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B. Atoms with the same number of protons and electrons but a different number
of neutrons
C. Oxygen often forms isotopes (O16, O17, and O18)
D. Unstable isotopes are radioactive; they emit energy or atomic fragments
Molecules and Compounds
A. Molecule: particle formed when two or more atoms chemically combine
B. Compound: particle formed when two or more atoms of different elements
chemically combine
C. Molecular formula: depict the elements present and the number of each atom
present in the molecule
Bonding of Atoms
A. Bonds form when atoms combine with other atoms
B. Electrons of an atom occupy regions of space called electron shells which
circle the nucleus
C. For atoms with atomic numbers of 18 or less, the following rules apply:
1. The first shell can hold up to 2 electrons
2. The second shell can hold up to 8 electrons
3. The third shell can hold up to 8 electrons
2.1 From Science to Technology: Radioactive Isotopes Reveal Physiology
2.2 From Science to Technology: Ionizing Radiation
Bonding of Atoms
A. Lower shells are filled first
B. If the outermost shell is full, the atom is stable
Bonding of Atoms: Ions
A. Ions
1. An atom that gains or loses electrons to become stable
2. An electrically charged atom
B. Cations
1. A positively charged ion
2. Formed when an atom loses electrons
C. Anions
1. A negatively charged ion
2. Formed when an atom gains electrons
Ionic Bonds
A. An attraction between a cation and an anion
B. Formed when electrons are transferred from one atom to another atom
Covalent Bonds
A. Formed when atoms share electrons
1. Hydrogen atoms form single bonds
2. Oxygen atoms form two bonds
3. Nitrogen atoms form three bonds
4. Carbon atoms form four bonds
Bonding of Atoms: Structural Formula
A. Structural formulas show how atoms bond and are arranged in various
molecules
C. Hormones
D. Receptors
E. Enzymes
F. Antibodies
G. Protein building blocks are amino acids
H. Amino acids held together with peptide bonds
Organic Substances: Nucleic Acids
A. Carry genes
B. Encode amino acid sequences of proteins
C. Building blocks are nucleotides
D. DNA (deoxyribonucleic acid) double polynucleotide
E. RNA (ribonucleic acid) single polynucleotide
2.3 From Science to Technology: CT Scanning and PET Imaging
Outcomes to be Assessed
2.1: Introduction
Give examples of how the study of living materials requires and understanding of
chemistry.
2.2: Structure of Matter
Describe how atomic structure determines how atoms interact.
Describe the relationships among matter, atoms, and molecules.
Explain how molecular and structural formulas symbolize the composition of
compounds.
Describe three types of chemical reactions.
Explain what acids, bases, and buffers are.
Define pH.
2.3: Chemical Constituents of Cells
List the major groups of inorganic chemicals common in cells.
Describe the general functions of the main classes of organic molecules in cells.
3. Rough ER
a. Studded with ribosomes
4. Smooth ER
a. Lipid synthesis
1). Added to proteins arriving from rough ER
b. Break down of drugs
B. Ribosomes
1. Free floating or connected to ER
2. Provide structural support and enzyme activity to amino acids to form
protein
C. Golgi apparatus
1. Stack of flattened, membranous sacs
2. Modifies, packages and delivers proteins
D. Vesicles
1. Membranous sacs
2. Store substances
E. Mitochondria
1. Membranous sacs with inner partitions
2. Generate energy
F. Lysosomes
1. Enzyme-containing sacs
2. Digest worn out cell parts or unwanted substances
G. Peroxisomes
1. Enzyme-containing sacs
2. Break down organic molecules
H. Centrosome
1. Two rod-like centrioles
2. Used to produce cilia and flagella
3. Distributes chromosomes during cell division
I. Cilia
1. Short hair-like projections
2. Propel substances on cell surface
J. Flagellum
1. Long tail-like projection
2. Provides motility to sperm
K. Microfilaments and microtubules
1. Thin rods and tubules
2. Support cytoplasm
3. Allows for movement of organelles
L. Inclusions
1. Temporary nutrients and pigments
3.2 Clinical Application: Disease at the Organelle Level
Cell Nucleus
A. Is the control center of the cell
B. Nuclear envelope
1. Porous double membrane
Outcomes to be Assessed
3.1: Introduction
Define cell.
State the range of cell numbers and cells sizes in a human body.
State the term for cell specialization.
3.2: A Composite Cell
List the three major parts of a composite cell.
State the general function of organelles.
Explain how the structure of a cell membrane makes possible its function.
Describe each type of organelle, and explain its function.
Describe the parts of a cell nucleus and their functions.
3.3: Movement Into and Out of the Cell
Explain the various ways that substances move through the cell membrane.
Discuss how the mechanisms of crossing cell membranes differ.
3.4: The Cell Cycle
Describe the parts of the cell cycle and identify the major activities during each
part.
Explain why regulation of the cell cycle is important to health.
Distinguish between mitosis and cytokinesis.
List the stages of mitosis and describe the events of each stage.
3.5: Control of Cell Division
Explain how different types of cells differ in their rate of cells division.
State the range of cell divisions a cell typically undergoes.
Discuss factors that influence whether or not a cell divides.
Explain how cancer arises from too-frequent cell division.
Distinguish the two types of genetic control of cancer.
3.6: Stem and Progenitor Cells
Define differentiation.
Distinguish between a stem cell and a progenitor cell.
Explain how two differentiated cell types can have the same genetic information,
but different appearances and functions.
3.7: Cell Death
Define apoptosis.
Distinguish apoptosis from necrosis.
List the steps of apoptosis.
Describe the relationship between apoptosis and mitosis.
Cellular Respiration
A. Produces:
1. Carbon dioxide
2. Water
3. ATP (chemical energy)
4. Heat
B. Includes:
1. Anaerobic reactions (without O2) - produce little ATP
2. Aerobic reactions (requires O2) - produce most ATP
Glycolysis
A. Series of ten reactions
B. Breaks down glucose into 2 pyruvic acid molecules
C. Occurs in cytosol
D. Anaerobic phase of cellular respiration
E. Yields two ATP molecules per glucose molecule
F. Summarized by three main phases or events:
1. Phosphorylation
2. Splitting
3. Production of NADH and ATP
Anaerobic Reactions
A. Event 1 - Phosphorylation
1. Two phosphates added to glucose
2. Requires ATP
B. Event 2 Splitting (cleavage)
1. 6-carbon glucose split into two 3-carbon molecules
C. Event 3 Production of NADH and ATP
1. Hydrogen atoms are released
2. Hydrogen atoms bind to NAD+ to produce NADH
3. NADH delivers hydrogen atoms to electron transport system if oxygen
is available
4. ADP is phosphorylated to become ATP
5. Two molecules of pyruvic acid are produced
6. Two molecules of ATP are generated
D. If oxygen is not available:
1. Electron transport system cannot accept new electrons from NADH
2. Pyruvic acid is converted to lactic acid
3. Glycolysis is inhibited
4. ATP production is less than in aerobic reactions
Aerobic Reactions
A. If oxygen is available:
1. Pyruvic acid is used to produce acetyl CoA
2. Citric acid cycle begins
3. Electron transport system functions
4. Carbon dioxide and water are formed
5. 34 molecules of ATP are produced per each glucose molecule
Genetic Code
A. Specification of the correct sequence of amino acids in a polypeptide chain
B. Each amino acid is represented by a triplet code
RNA Molecules
A. Messenger RNA (mRNA):
1. Making of mRNA (copying of DNA) is transcription
B. Transfer RNA (tRNA):
1. Carries amino acids to mRNA
2. Carries anticodon to mRNA
3. Translates a codon of mRNA into an amino acid
C. Ribosomal RNA (rRNA):
1. Provides structure and enzyme activity for ribosomes
D. Messenger RNA (mRNA):
1. Delivers genetic information from nucleus to the cytoplasm
2. Single polynucleotide chain
3. Formed beside a strand of DNA
4. RNA nucleotides are complementary to DNA nucleotides (exception
no thymine in RNA; replaced with uracil)
Protein Synthesis
4.3 From Science to Technology: MicroRNAs and RNA Interference
4.7: Changes in Genetic Information
A. Only about 1/10th of one percent of the human genome differs from person to
person
Nature of Mutations
A. Mutations change in genetic information
B. Result when:
1. Extra bases are added or deleted
2. Bases are changed
C. May or may not change the protein
Protection Against Mutation
A. Repair enzymes correct the mutations
Inborn Errors of Metabolism
A. Occurs from inheriting a mutation that then alters an enzyme
B. This creates a block in an otherwise normal biochemical pathway
4.4 From Science to Technology: The Human Metabolome
Outcomes to be Assessed
4.1: Introduction
Define metabolism.
Explain why protein synthesis is important.
4.2: Metabolic Processes
Compare and contrast anabolism and catabolism.
Define dehydration synthesis and hydrolysis.
4.3: Control of Metabolic Reactions
Describe how enzymes control metabolic reactions.
List the basic steps of an enzyme-catalyzed reaction.
Define active site.
3. Cover ovaries
4. Line ducts of some glands
C. Simple columnar:
1. Single layer of elongated cells
2. Nuclei usually near the basement
3. Membrane at same level
4. Sometimes possess cilia
5. Sometimes possess microvilli
6. Often have goblet cells
7. Line uterus, stomach, intestines
D. Pseudostratified columnar:
1. Single layer of elongated cells
2. Nuclei at two or more levels
3. Appear striated
4. Often have cilia
5. Often have goblet cells
6. Line respiratory passageways
E. Stratified squamous:
1. Many cell layers
2. Top cells are flat
3. Can accumulate keratin
4. Outer layer of skin
5. Line oral cavity, vagina, and anal canal
F. Stratified cuboidal:
1. 2-3 layers
2. Cube-shaped cells
3. Line ducts of mammary glands, sweat glands, salivary glands, and
the pancreas
G. Stratified columnar:
1. Top layer of elongated cells
2. Cube-shaped cells in deeper layers
3. Line part of male urethra and part of pharynx
H. Transitional:
1. Many cell layers
2. Cube-shaped and elongated cells
3. Line urinary bladder, ureters, and part of urethra
Glandular Epithelium
A. Composed of cells that are specialized to produce and secrete substances
B. There are two (2) types:
1. Endocrine glands are ductless (key word: hormone)
2. Exocrine glands have ducts
a. Unicellular exocrine gland:
1.) Composed of one cell
2.) Goblet cell
b. Multicellular exocrine gland:
1.) Composed of many cells
3.) Striated
4.) Intercalated discs
5.6: Nervous Tissue
A. Found in brain, spinal cord, and peripheral nerves
B. Functional cells are neurons
C. Neuroglial cells support and bind nervous tissue components
D. Sensory reception
E. Conduction of nerve impulses
5.2 From Science to Technology: Tissue Engineering: Replacement Bladders and Hearts
Outcomes to be Assessed
5.1: Introduction
Describe a tissue, and explain the intercellular junctions found in tissues.
List the four major tissue types in the body.
5.2: Epithelial Tissues
Describe the general characteristics and functions of epithelial tissue.
Name the types of epithelium and identify and organ in which each is found.
Explain how glands are classified.
5.3: Connective Tissues
Describe the general characteristics of connective tissue.
Compare and contrast the cellular components, structures, fibers, and
extracellular matrix (where applicable) in each type of connective tissue.
Describe the major functions of each type of connective tissue.
5.4: Types of Membranes
Describe and locate each of the four types of membranes.
5.5: Muscle Tissues
Distinguish among the three types of muscle tissue.
5.6: Nervous Tissues
Describe the general characteristics and functions of nervous tissue.
B. Tube-like depression
C. Extends into dermis
D. Three (3) parts:
1. Hair root
2. Hair shaft
3. Hair papilla
E. Dead epidermal cells
F. Melanin
G. Arrector pili muscle
Nails
A. Protective coverings
B. Three (3) parts:
1. Nail plate
2. Nail bed
3. Lunula
6.2 Clinical Application: Hair Loss
Sebaceous Glands
A. Usually associated with hair follicles
B. Holocrine glands
C. Secrete sebum (oil)
D. Absent on palms and soles
Sweat Glands
A. Aka sudoriferous glands
B. Widespread in skin
C. Originates in deeper dermis or hypodermis
D. Eccrine glands
E. Apocrine glands
F. Ceruminous glands
G. Mammary glands
6.3 Clinical Application: Acne
6.4: Regulation of Body Temperature
A. Regulation of body temperature is vitally important because even slight shifts
can disrupt metabolic reactions.
Heat Production and Loss
A. Heat is a product of cellular metabolism
1. The most active body cells are the heat producers and include:
a. Skeletal muscle
b. Cardiac muscle
c. Cells of certain glands such as the liver
B. The primary means of heat loss is radiation
1. Also there is conduction, convection and evaporation
Problems in Temperature Regulation
A. Hyperthermia abnormally high body temperature
B. Hypothermia abnormally low body temperature
6.4 Clinical Application: Elevated Body Temperature
6.5: Healing of Wounds and Burns
B. Central canal
C. Perforating canal aka Volkmanns canal
D. Osteocytes
E. Lamellae
F. Lacunae
G. Bone matrix
H. Canaliculi
Spongy Bone
A. Spongy bone is aka cancellous bone
7.3: Bone Development and Growth
A. Parts of the skeletal system begin to develop during the first few weeks of
prenatal development
B. Bones replace existing connective tissue in one of two ways:
1. As intramembranous bones
2. As endchondral bones
Intramembranous Bones
A. Intramembranous Bones
B. These bones originate within sheetlike layers of connective tissues
C. They are the broad, flat bones
1. Skull bones (except mandible)
D. Are known as intramembranous bones
Endochondral Bones
A. Endochondral Bones
B. Bones begin as hyaline cartilage
1. Form models for future bones
C. These are most bones of the skeleton
D. Are known as endochondral bones
Endochondral Ossification
A. Hyaline cartilage model
B. Primary ossification center
C. Secondary ossification centers
D. Epiphyseal plate
E. Osteoblasts vs. osteoclasts
Growth at the Epiphyseal Plate
A. First layer of cells
1. Closest to the end of epiphysis
2. Resting cells
3. Anchors epiphyseal plate to epiphysis
B. Second layer of cells
1. Many rows of young cells
2. Undergoing mitosis
C. Third layer of cells
1. Older cells
2. Left behind when new cells appear
3. Cells enlarging and becoming calcified
D. Fourth layer of cells
1. Thin
2. Dead cells
3. Calcified extracellular matrix
Homeostasis of Bone Tissue
A. Bone Resorption action of osteoclasts and parathyroid hormone aka
parathormone aka PTH
B. Bone Deposition action of osteoblasts and calcitonin
C. Occurs by direction of the thyroid and parathyroid glands
Factors Affecting Bone Development, Growth and Repair
A. Deficiency of Vitamin A retards bone development
B. Deficiency of Vitamin C results in fragile bones
C. Deficiency of Vitamin D rickets, osteomalacia
D. Insufficient Growth Hormone dwarfism
E. Excessive Growth Hormone gigantism, acromegaly
F. Insufficient Thyroid Hormone delays bone growth
G. Sex Hormones promote bone formation; stimulate ossification of epiphyseal
plates
H. Physical Stress stimulates bone growth
7.1 Clinical Application: Fractures
7.4: Bone Function
A. Bones shape, support, and protect body structures
Support, Protection, and Movement
A. Gives shape to head, etc.
B. Supports bodys weight
C. Protects lungs, etc.
D. Bones and muscles interact
E. When limbs or body parts move
Blood Cell Formation
A. Also known as hematopoiesis
B. Occurs in the red bone marrow
Inorganic Salt Storage
A. Calcium
B. Phosphate
C. Magnesium
D. Sodium
E. Potassium
7.2 Clinical Application: Osteopenia and Osteoporosis: Preventing Fragility Fractures
7.5: Skeletal Organization
A. The actual number of bones in the human skeleton varies from person to
person
B. Typically there are about 206 bones
C. For convenience the skeleton is divided into the:
1. Axial skeleton
2. Appendicular skeleton
Divisions of the Skeleton
A. Axial Skeleton
1. Skull
2. Spine
3. Rib cage
B. Appendicular Skeleton
1. Upper limbs
2. Lower limbs
3. Shoulder girdle
4. Pelvic girdle
7.6: Skull
A. Is composed of the cranium (brain case) and the facial bones
1. Frontal Bone (1)
a. Forehead
b. Roof of nasal cavity
c. Roofs of orbits
d. Frontal sinuses
e. Supraorbital foramen
f. Coronal suture
2. Parietal Bones (2)
a. Side walls of cranium
b. Roof of cranium
c. Sagittal suture
3. Occipital Bone (1)
a. Back of skull
b. Base of cranium
c. Foramen magnum
d. Occipital condyles
e. Lambdoidal suture
4. Temporal Bones (2)
a. Side walls of cranium
b. Floor of cranium
c. Floors and sides of orbits
d. Squamous suture
e. External acoustic meatus
f. Mandibular fossa
g. Mastoid process
h. Styloid process
i. Zygomatic process
5. Sphenoid Bone (1)
a. Base of cranium
b. Sides of skull
c. Floors and sides of orbits
d. Sella turcica
e. Sphenoid sinuses
6. Ethmoid Bone (1)
a. Roof and walls of nasal cavity
b. Floor of cranium
c. Wall of orbits
d. Cribiform plates
e. Perpendicular plate
f. Superior and middle nasal conchae
g. Ethmoid sinuses
h. Crista galli
7. Maxillary Bones (2)
a. Upper jaw
b. Anterior roof of mouth
c. Floors of orbits
d. Sides of nasal cavity
e. Floors of nasal cavity
f. Alveolar processes
g. Maxillary sinuses
h. Palatine process
8. Palatine Bones (2)
a. L shaped bones located behind the maxillae
b. Posterior section of hard palate
c. Floor of nasal cavity
d. Lateral walls of nasal cavity
9. Zygomatic Bones (2)
a. Prominences of cheeks
b. Lateral walls of orbits
c. Floors of orbits
d. Temporal process
10. Lacrimal Bones (2)
a. Medial walls of orbits
b. Groove from orbit to nasal cavity
11. Nasal Bones (2)
a. Bridge of nose
12. Vomer Bone (1)
a. Inferior portion of nasal septum
13. Inferior Nasal Conchae (2)
a. Extend from lateral walls of nasal cavity
14. Mandible Bone (1)
a. Lower jaw
b. Body
c. Ramus
d. Mandibular condyle
e. Coronoid process
f. Alveolar process
g. Mandibular foramen
h. Mental foramen
Infantile Skull
A. Fontanels fibrous membranes
7.7: Vertebral Column
A. Aka tailbone
B. 3-4 fused segments
7.3 Clinical Application: Disorders of the Vertebral Column
7.8: Thoracic Cage
A. The thoracic cage includes the ribs, the thoracic vertebrae, the sternum, and the
costal cartilages that attach the ribs to the sternum.
1. Ribs (12)
2. Sternum
3. Thoracic vertebrae (12)
4. Costal cartilages
5. Supports shoulder girdle and upper limbs
6. Protects viscera
7. Role in breathing
Ribs
A. Humans have 12 pairs of ribs:
1. True ribs (7)
2. False ribs (5), of which:
a. Floating (2)
B. There are some anomalies:
1. Cervical ribs
2. Lumbar ribs
Rib Structure
A. Shaft
B. Head posterior end; articulates with vertebrae
C. Tubercle articulates with vertebrae
D. Costal cartilage hyaline cartilage
Sternum
A. Three (3) parts of the sternum:
1. Manubrium
2. Body
3. Xiphoid process
7.9: Pectoral Girdle
A. Also known as the shoulder girdle
B. Clavicles
C. Scapulae
D. Supports upper limbs
E. True shoulder joint is simply the articulation of the humerus and scapula
Clavicles
A. Articulate with manubrium
B. Articulate with scapulae (acromion process)
C. A-C joint
Scapulae
A. Spine
B. Supraspinous fossa
C. Infraspinous fossa
D. Acromion process
E. Coracoid process
F. Glenoid fossa or cavity
7.10: Upper Limb
A. Humerus
B. Radius
C. Ulna
D. (Interosseous membrane)
E. Carpals
F. Metacarpals
G. Phalanges
Humerus
A. Head
B. Greater tubercle
C. Lesser tubercle
D. Anatomical neck
E. Surgical neck
F. Deltoid tuberosity
G. Capitulum
H. Trochlea
I. Coronoid fossa
J. Olecranon fossa
Radius
A. Lateral forearm bone
B. Head
C. Radial tuberosity
D. Styloid process
Ulna
A. Medial forearm bone
B. Trochlear notch
C. Olecranon process
D. Coronoid process
E. Styloid process
Wrist and Hand
A. Carpal Bones (16 total bones)
1. Scaphoid
2. Lunate
3. Triquetral
4. Pisiform
5. Hamate
6. Capitate
7. Trapezoid
8. Trapezium
B. Metacarpal Bones (10)
C. Phalangeal Bones (28)
1. Proximal phalanx
2. Middle phalanx
3. Distal phalanx
7.11: Pelvic Girdle
A. Coxal Bones (2)
1. Supports trunk of body
2. Protects viscera
3. Forms pelvic cavity
Hip Bones
A. Also known as the coxae:
1. Acetabulum
2. There are three (3) bones:
a. Ilium
1.) Iliac crest
2.) Iliac spines
3.) Greater sciatic notch
b. Ischium
1.) Ischial spines
2.) Lesser sciatic notch
3.) Ischial tuberosity
c. Pubis
1.) Obturator foramen
2.) Symphysis pubis
3.) Pubic arch
Greater and Lesser Pelves
A. Greater Pelvis
1. Lumbar vertebrae posteriorly
2. Iliac bones laterally
3. Abdominal wall anteriorly
B. Lesser Pelvis
1. Sacrum and coccyx posteriorly
2. Lower ilium, ischium, and pubic bones laterally and anteriorly
Differences Between Male Female Pelves
A. Female pelvis
1. Iliac bones more flared
2. Broader hips
3. Pubic arch angle greater
4. More distance between ischial spines and ischial tuberosities
5. Sacral curvature shorter and flatter
6. Lighter bones
7. Why?
7.12: Lower Limb
A. Femur
B. Patella
C. Tibia
D. Fibula
E. Tarsals
F. Metatarsals
G. Phalanges
Femur
A. Longest bone of body
B. Head
C. Fovea capitis
D. Neck
E. Greater trochanter
F. Lesser trochanter
G. Linea aspera
H. Condyles
I. Epicondyles
Patella
A. Aka kneecap
B. Anterior surface of the knee joint
C. Flat sesamoid bone located in the quadriceps tendon
Tibia
A. Aka shin bone
B. Medial to fibula
C. Condyles
D. Tibial tuberosity
E. Anterior crest
F. Makes the medial malleolus
Fibula
A. Lateral to tibia
B. Long, slender
C. Head
D. Makes the lateral malleolus
E. Non-weight bearing
Foot
A. Tarsal Bones (14)
1. Calcaneus
2. Talus
3. Navicular
4. Cuboid
5. Lateral (3rd) cuneiform
6. Intermediate (2nd) cuneiform
7. Medial (1st) cuneiform
B. Metatarsal Bones (10)
C. Phalanges (28)
1. Proximal
2. Middle
3. Distal
7.13: Lifespan Changes
A. Decrease in height at about age 30
B. Calcium levels fall
C. Bones become brittle
F. Gliding Joint
1. Between carpals
2. Between tarsals
3. Between facets of adjacent vertebrae
8.5: Types of Joint Movements
A. Movement at a joint occurs when a muscle contracts and its fibers pull its
moveable end (insertion) towards its fixed end (origin).
Types of Joint Movements
A. Abduction/adduction
B. Dorsiflexion/plantar flexion
C. Flexion/extension/hyperextension
D. Lateral flexion
E. Rotation
F. Circumduction
G. Supination/pronation
H. Eversion/inversion
I. Protraction/retraction
J. Elevation/depression
8.6: Examples of Synovial Joints
A. The shoulder, elbow, hip, and knee are large, freely moveable joints.
Shoulder Joint
A. Ball-and-socket
B. Head of humerus and glenoid cavity of scapula
C. Loose joint capsule
D. Bursae
E. Ligaments prevent displacement
F. Very wide range of movement (circumduction)
Elbow Joint
A. Hinge joint
1. Trochlea of humerus
2. Trochlear notch of ulna
B. Gliding joint
1. Capitulum of humerus
2. Head of radius
C. Flexion and extension
D. Many reinforcing ligaments
E. Stable joint
Hip Joint
A. Ball-and-socket joint
B. Head of femur and acetabulum of coxa
C. Heavy joint capsule
D. Many reinforcing ligaments
E. Less freedom of movement than shoulder joint
F. Circumduction
Knee Joint
A. Largest joint
B. Most complex
C. Medial and lateral condyles of distal end of femur and
D. Medial and lateral condyles of proximal end of tibia and
E. Femur articulates anteriorly with patella
F. Strengthened by many ligaments and tendons
G. Menisci separate femur and tibia
H. Bursae
8.1 Clinical Application: Replacing Joints
8.2 Clinical Application: Joint Disorders
8.7: Lifespan Changes
A. Joint stiffness is an early sign of aging
B. Fibrous joints first to change; can strengthen however over a lifetime
C. Changes in symphysis joints of vertebral column diminish flexibility and
decrease height (remember water loss from the IVDs)
D. Synovial joints lose elasticity
E. Disuse hampers the blood supply
F. Activity and exercise can keep joints functional longer
Outcomes to be Assessed
8.1: Introduction
List the functions of joints.
8.2: Classification of Joints
Explain how joints can be classified according the type of tissue that binds the
bones together.
Describe how bones of fibrous joints are held together.
Describe how bones of cartilaginous joints are held together.
8.3: General Structure of a Synovial Joint
Describe the general structure of a synovial joint.
8.4: Types of Synovial Joints
Distinguish among the six types of synovial joints and give an example of each
type.
8.5: Types of Joint Movements
Explain how skeletal muscles produce movements at joints, and identify several
types of joint movements.
8.6: Examples of Synovial Joints
Describe the shoulder joint and explain how its articulating parts are held
together.
Describe the elbow, hip, and knee joints and explain how their articulating parts
are held together.
8.7: Lifespan Changes
Describe lifespan changes in joints.
B. Sacroplasm
C. Sarcoplasmic reticulum (SR)
D. Transverse (T) tubule
E. Triad
1. Cisternae of SR
2. T tubule
F. Myofibril
G. Actin myofilaments
H. Myosin myofilaments
I. Sarcomere
9.3: Skeletal Muscle Contraction
A. Movement within the myofilaments
B. I band (thin)
C. A band (thick and thin)
D. H zone (thick)
E. Z line (or disc)
F. M line
Myofilaments
A. Thick myofilaments
1. Composed of myosin protein
2. Form the cross-bridges
B. Thin myofilaments
1. Composed of actin protein
2. Associated with troponin and tropomyosin proteins
Neuromuscular Junction
A. Also known as NMJ or myoneural junction
B. Site where an axon and muscle fiber meet
C. Parts to know:
1. Motor neuron
2. Motor end plate
3. Synapse
4. Synaptic cleft
5. Synaptic vesicles
6. Neurotransmitters
Motor Unit
A. Single motor neuron
B. All muscle fibers controlled by motor neuron
C. As few as four fibers
D. As many as 1000s of muscle fibers
Stimulus for Contraction
A. Acetylcholine (ACh)
B. Nerve impulse causes release of ACh from synaptic vesicles
C. ACh binds to ACh receptors on motor end plate
D. Generates a muscle impulse
E. Muscle impulse eventually reaches the SR and the cisternae
9.1 Clinical Application: Myasthenia Gravis
Excitation-Contraction Coupling
A. Muscle impulses cause SR to release calcium ions into cytosol
B. Calcium binds to troponin to change its shape
C. The position of tropomyosin is altered
D. Binding sites on actin are now exposed
E. Actin and myosin molecules bind via myosin cross-bridges
The Sliding Filament Model of Muscle Contraction
A. When sarcromeres shorten, thick and thin filaments slide past one another
B. H zones and I bands narrow
C. Z lines move closer together
Cross Bridge Cycling
A. Myosin cross-bridge attaches to actin binding site
B. Myosin cross-bridge pulls thin filament
C. ADP and phosphate released from myosin
D. New ATP binds to myosin
E. Linkage between actin and myosin cross-bridge break
F. ATP splits
G. Myosin cross-bridge goes back to original position
Relaxation
A. Acetylcholinesterase rapidly decomposes Ach remaining in the synapse
B. Muscle impulse stops
C. Stimulus to sarcolemma and muscle fiber membrane ceases
D. Calcium moves back into sarcoplasmic reticulum (SR)
E. Myosin and actin binding prevented
F. Muscle fiber relaxes
Energy Sources for Contraction
A. 1) Creatine phosphate and 2) Cellular respiration
B. Creatine phosphate stores energy that quickly converts ADP to ATP
Oxygen Supply and Cellular Respiration
A. Cellular respiration:
1. Anaerobic Phase
a. Glycolysis
b. Occurs in cytoplasm
c. Produces little ATP
2. Aerobic Phase
a. Citric acid cycle
b. Electron transport system
c. Occurs in the mitochondria
d. Produces most ATP
e. Myoglobin stores extra oxygen
Oxygen Debt
A. Oxygen debt amount of oxygen needed by liver cells to use the accumulated
lactic acid to produce glucose
1. Oxygen not available
2. Glycolysis continues
3. Pyruvic acid converted to lactic acid
Outcomes to be Assessed
9.1: Introduction
List various outcomes of muscle action.
9.2: Structure of a Skeletal Muscle
Describe how connective tissue is a part of the structure of a skeletal muscle.
Name the major parts of a skeletal muscle fiber and describe the functions of
each.
9.3: Skeletal Muscle Contraction
Describe the neural control of skeletal muscle contraction.
Identify the major events that occur during skeletal muscle fiber contraction.
List the energy sources for skeletal muscle fiber contraction.
Describe how a muscle may become fatigued.
Describe oxygen debt.
9.4: Muscular Responses
Distinguish between fast and slow twitch muscle fibers.
Distinguish between a twitch and a sustained contraction.
Describe how exercise affects skeletal muscles.
Explain how various types of muscular contractions produce body movements
and help maintain posture.
9.5: Smooth Muscle
Distinguish between the structures and functions of multiunit smooth muscle and
visceral smooth muscle.
Compare the contraction mechanisms of skeletal and smooth muscle fibers.
9.6: Cardiac Muscle
Compare the contraction mechanisms of skeletal and cardiac muscle fibers.
9.7: Skeletal Muscle Actions
Explain how the attachments, locations, and interactions of skeletal muscles
make possible certain movements.
9.8: Major Skeletal Muscles
Identify and locate the skeletal muscles of each body region and describe the
action (s) of each muscle.
B. They may differ in length and size of their axons and dendrites
C. Neurons share certain features:
1. Dendrites
2. A cell body
3. An axon
Myelination of Axons
A. White Matter
1. Contains myelinated axons
2. Considered fiber tracts
B. Gray Matter
1. Contains unmyelinated structures
2. Cell bodies, dendrites
10.2 Clinical Application: Multiple Sclerosis
10.4: Classification of Neurons and Neuroglia
A. Neurons vary in function
1. They can be sensory, motor, or integrative neurons
B. Neurons vary in size and shape, and in the number of axons and dendrites that
they may have
C. Due to structural differences, neurons can be classified into three (3) major
groups:
1. Bipolar neurons
2. Unipolar neurons
3. Multipolar neurons
Classification of Neurons: Structural Differences
A. Bipolar neurons
1. Two processes
2. Eyes, ears, nose
B. Unipolar neurons
1. One process
2. Ganglia of PNS
3. Sensory
C. Multipolar neurons
1. 99% of neurons
2. Many processes
3. Most neurons of CNS
Classification of Neurons: Functional Differences
A. Sensory Neurons
1. Afferent
2. Carry impulse to CNS
3. Most are unipolar
4. Some are bipolar
B. Interneurons
1. Link neurons
2. Aka association neurons or internuncial neurons
3. Multipolar
4. Located in CNS
C. Motor Neurons
1. Multipolar
2. Carry impulses away from CNS
3. Carry impulses to effectors
Types of Neuroglial Cells in the PNS
A. Schwann Cells
1. Produce myelin found on peripheral myelinated neurons
2. Speed up neurotransmission
B. Satellite Cells
1. Support clusters of neuron cell bodies (ganglia)
Types of Neuroglial Cells in the CNS
A. Microglia
1. CNS
2. Phagocytic cell
B. Astrocytes
1. CNS
2. Scar tissue
3. Mop up excess ions, etc.
4. Induce synapse formation
5. Connect neurons to blood vessels
C. Oligodendrocytes
1. CNS
2. Myelinating cell
D. Ependyma or ependymal
1. CNS
2. Ciliated
3. Line central canal of spinal cord
4. Line ventricles of brain
Regeneration of A Nerve Axon
10.5: The Synapse
A. Nerve impulses pass from neuron to neuron at synapses, moving from a presynaptic neuron to a post-synaptic neuron.
Synaptic Transmission
A. Neurotransmitters are released when impulse reaches synaptic knob
10.6: Cell Membrane Potential
A. A cell membrane is usually electrically charged, or polarized, so that the inside
of the membrane is negatively charged with respect to the outside of the
membrane (which is then positively charged).
B. This is as a result of unequal distribution of ions on the inside and the outside
of the membrane.
Distribution of Ions
A. Potassium (K+) ions are the major intracellular positive ions (cations).
B. Sodium (Na+) ions are the major extracellular positive ions (cations).
C. This distribution is largely created by the Sodium/Potassium Pump (Na+/K+
pump).
D. This pump actively transports sodium ions out of the cell and potassium ions
into the cell.
Resting Potential
A. Resting Membrane Potential (RMP):
1. 70 mV difference from inside to outside of cell
2. It is a polarized membrane
3. Inside of cell is negative relative to the outside of the cell
4. RMP = -70 mV
5. Due to distribution of ions inside vs. outside
6. Na+/K+ pump restores
Local Potential Changes
A. Caused by various stimuli:
1. Temperature changes
2. Light
3. Pressure
B. Environmental changes affect the membrane potential by opening a gated ion
channel
C. Channels are 1) chemically gated, 2) voltage gated, or 3) mechanically gated
D. If membrane potential becomes more negative, it has hyperpolarized
E. If membrane potential becomes less negative, it has depolarized
F. Graded (or proportional) to intensity of stimulation reaching threshold potential
G. Reaching threshold potential results in a nerve impulse, starting an action
potential
Action Potentials
A. At rest, the membrane is polarized (RMP = -70)
B. Threshold stimulus reached (-55)
C. Sodium channels open and membrane depolarizes (toward 0)
D. Potassium leaves cytoplasm and membrane repolarizes (+30)
E. Brief period of hyperpolarization (-90)
All-or-None Response
A. If a neuron responds at all, it responds completely
B. A nerve impulse is conducted whenever a stimulus of threshold intensity or
above is applied to an axon
C. All impulses carried on an axon are the same strength
Refractory Period
A. Absolute Refractory Period
1. Time when threshold stimulus does not start another action potential
B. Relative Refractory Period
1. Time when stronger threshold stimulus can start another action potential
10.3 Clinical Application: Factors Affecting Impulse Conduction
10.7: Synaptic Transmission
A. This is where released neurotransmitters cross the synaptic cleft and react with
specific molecules called receptors in the postsynaptic neuron membrane.
B. Effects of neurotransmitters vary.
C. Some neurotransmitters may open ion channels and others may close ion
channels.
Synaptic Potentials
A. EPSP
1. Excitatory postsynaptic potential
2. Graded
3. Depolarizes membrane of postsynaptic neuron
4. Action potential of postsynaptic neuron becomes more likely
B. IPSP
1. Inhibitory postsynaptic potential
2. Graded
3. Hyperpolarizes membrane of postsynaptic neuron
4. Action potential of postsynaptic neuron becomes less likely
Summation of EPSPs and IPSPs
A. EPSPs and IPSPs are added together in a process called summation
B. More EPSPs lead to greater probability of an action potential
Neurotransmitters
Neuropeptides
A. Neurons in the brain or spinal cord synthesize neuropeptides.
B. These neuropeptides act as neurotransmitters.
C. Examples include:
1. Enkephalins
2. Beta endorphin
3. Substance P
10.4 Clinical Application: Opiates in the Human Body
10.8: Impulse Processing
A. Way the nervous system processes nerve impulses and acts upon them
1. Neuronal Pools
a. Interneurons
b. Work together to perform a common function
c. May excite or inhibit
2. Convergence
a. Various sensory receptors
b. Can allow for summation of impulses
3. Divergence
a. Branching axon
b. Stimulation of many neurons ultimately
Neuronal Pools
A. Groups of interneurons that make synaptic connections with each other
B. Interneurons work together to perform a common function
C. Each pool receives input from other neurons
D. Each pool generates output to other neurons
Convergence
A. Neuron receives input from several neurons
B. Incoming impulses represent information from different types of sensory
receptors
C. Allows nervous system to collect, process, and respond to information
D. Makes it possible for a neuron to sum impulses from different sources
Divergence
A. One neuron sends impulses to several neurons
B. Can amplify an impulse
C. Impulse from a single neuron in CNS may be amplified to activate enough
motor units needed for muscle contraction
Outcomes to be Assessed
10.1: Introduction
Describe the general functions of the nervous system.
Identify the two types of cells that comprise nervous tissue.
Identify the two major groups of nervous system organs.
10.2: General Functions of the Nervous System
List the functions of sensory receptors.
Describe how the nervous system responds to stimuli.
10.3: Description of Cells of the Nervous System
Describe the three major parts of a neuron.
Define neurofibrils and chromatophilic substance.
Describe the relationship among myelin, the neurilemma, and the nodes of
Ranvier.
Distinguish between the sources of white matter and gray matter.
10.4: Classification of Neurons and Neuroglia
Identify structural and functional differences among neurons.
Identify the types of neuroglia in the central nervous system and their functions.
Describe the Schwann cells of the peripheral nervous system.
10.5: The Synapse
Define presynaptic and postsynaptic.
Explain how information passes from a presynaptic to a postsynaptic neuron.
10.6: Cell Membrane Potential
Explain how a cell membrane becomes polarized.
Define resting potential, local potential, and action potential.
Describe the events leading to the conduction of a nerve impulse.
Compare nerve impulse conduction in myelinated and unmyelinated neurons.
10.7: Synaptic Transmission
Identify the changes in membrane potential associated with excitatory and
inhibitory neurotransmitters.
10.8: Impulse Processing
Describe the basic ways in which the nervous system processes information.
11.5: Brain
A. Functions of the brain:
1. Interprets sensations
2. Determines perception
3. Stores memory
4. Reasoning
5. Makes decisions
6. Coordinates muscular movements
7. Regulates visceral activities
8. Determines personality
B. Major parts of the brain:
1. Cerebrum
a. Frontal lobes
b. Parietal lobes
c. Occipital lobes
d. Temporal lobes
e. Insula
2. Diencephalon
3. Cerebellum
4. Brainstem
a. Midbrain
b. Pons
c. Medulla oblongata
Brain Development
A. Neural tube
B. Three primary vesicles:
1. Forebrain (Prosencephalon)
2. Midbrain (Mesencephalon)
3. Hindbrain (Rhombencephalon)
C. Five secondary vesicles:
1. Telencephalon
2. Diencephalon
3. Mesencephalon
4. Metencephalon
5. Myelencephalon
Structure of the Cerebrum
A. Corpus callosum
1. Connects cerebral hemispheres (a commissure)
B. Gyri
1. Bumps or convolutions
C. Sulci
1. Grooves in gray matter
a. Central sulcus of Rolando
D. Fissures
1. Longitudinal: separates the cerebral hemispheres
2. Transverse: separates cerebrum from cerebellum
a. Understanding speech
b. Choosing words to express thought
3. Temporal lobe association areas
a. Interpret complex sensory experiences
b. Store memories of visual scenes, music, and complex patterns
4. Occipital lobe association areas
a. Analyze and combine visual images with other sensory
experiences
Motor Areas (pre-central sulcus)
A. Primary motor areas
1. Frontal lobes
2. Control voluntary muscles
B. Brocas area
1. Anterior to primary motor cortex
2. Usually in left hemisphere
3. Controls muscles needed for speech
C. Frontal eye field
1. Above Brocas area
2. Controls voluntary movements of eyes and eyelids
Hemisphere Dominance
A. The left hemisphere is dominant in most individuals
1. Dominant hemisphere controls:
a. Speech
b. Writing
c. Reading
d. Verbal skills
e. Analytical skills
f. Computational skills
2. Nondominant hemisphere controls:
a. Nonverbal tasks
b. Motor tasks
c. Understanding and interpreting musical and visual patterns
d. Provides emotional and intuitive thought processes
Memory
A. Short term memory
1. Working memory
2. Closed neuronal circuit
3. Circuit is stimulated over and over
4. When impulse flow ceases, memory does also unless it enters long-term
memory via memory consolidation
B. Long term memory
1. Changes structure or function of neurons
2. Enhances synaptic transmission
11.4 Clinical Application: Traumatic Brain Injury
Basal Nuclei
A. Masses of gray matter
C. Cerebral aqueduct
D. Cerebral peduncles (bundles of nerve fibers)
E. Corpora quadrigemina (centers for visual and auditory reflexes)
Pons
A. Rounded bulge on underside of brainstem
B. Between medulla oblongata and midbrain
C. Helps regulate rate and depth of breathing
D. Relays nerve impulses to and from medulla oblongata and cerebellum
Medulla Oblongata
A. Enlarged continuation of spinal cord
B. Conducts ascending and descending impulses between brain and spinal cord
C. Contains cardiac, vasomotor, and respiratory control centers
D. Contains various nonvital reflex control centers (coughing, sneezing,
swallowing, and vomiting)
Reticular Formation
A. Complex network of nerve fibers scattered throughout the brain stem
B. Extends into the diencephalon
C. Connects to centers of hypothalamus, basal nuclei, cerebellum, and cerebrum
D. Filters incoming sensory information
E. Arouses cerebral cortex into state of wakefulness
Types of Sleep
A. Slow wave
1. Non-REM sleep
2. Person is tired
3. Decreasing activity of reticular system
4. Restful
5. Dreamless
6. Reduced blood pressure and respiratory rate
7. Ranges from light to heavy
8. Alternates with REM sleep
B. Rapid Eye Movement (REM)
1. Paradoxical sleep
2. Some areas of brain active
3. Heart and respiratory rates irregular
4. Dreaming occurs
Cerebellum
A. Inferior to occipital lobes
B. Posterior to pons and medulla oblongata
C. Two hemispheres
D. Vermis connects hemispheres
E. Cerebellar cortex (gray matter)
F. Arbor vitae (white matter)
G. Cerebellar peduncles (nerve fiber tracts)
H. Dentate nucleus (largest nucleus in cerebellum)
I. Integrates sensory information concerning position of body parts
J. Coordinates skeletal muscle activity
K. Maintains posture
11.6 Clinical Application: Brain Waves
11.6: Peripheral Nervous System
A. Cranial nerves arising from the brain
1. Somatic fibers connecting to the skin and skeletal muscles
2. Autonomic fibers connecting to viscera
B. Spinal nerves arising from the spinal cord
1. Somatic fibers connecting to the skin and skeletal muscles
2. Autonomic fibers connecting to viscera
Nerve and Nerve Fiber Classification
A. Sensory nerves
1. Conduct impulses into brain or spinal cord
B. Motor nerves
1. Conduct impulses to muscles or glands
C. Mixed (both sensory and motor) nerves
1. Contain both sensory nerve fibers and motor nerve fibers
2. Most nerves are mixed nerves
3. ALL spinal nerves are mixed nerves (except the first pair)
Nerve Fiber Classification
A. General somatic efferent (GSE) fibers
1. Carry motor impulses from CNS to skeletal muscles
B. General visceral efferent (GVE) fibers
1. Carry motor impulses away from CNS to smooth muscles and glands
C. General somatic afferent (GSA) fibers
1. Carry sensory impulses to CNS from skin and skeletal muscles
D. General visceral afferent (GVA) fibers
1. Carry sensory impulses to CNS from blood vessels and internal organs
E. Special somatic efferent (SSE) fibers
1. Carry motor impulses from brain to muscles used in chewing,
swallowing, speaking and forming facial expressions
F. Special visceral afferent (SVA) fibers
1. Carry sensory impulses to brain from olfactory and taste receptors
G. Special somatic afferent (SSA) fibers
1. Carry sensory impulses to brain from receptors of sight, hearing and
equilibrium
Cranial Nerves
A. Remember:
1. Cranial nerves are designated C N
2. Cranial nerves are designated with Roman numerals (I XII)
Cranial Nerves I and II
A. Olfactory nerve (CN I)
1. Sensory nerve
2. Fibers transmit impulses associated with smell
B. Optic nerve (CN II)
1. Sensory nerve
2. Fibers transmit impulses associated with vision
A. Cholinergic fibers
1. Release acetylcholine
2. Preganglionic sympathetic and parasympathetic fibers
3. Postganglionic parasympathetic fibers
B. Adrenergic fibers
1. Release norepinephrine
2. Most postganglionic sympathetic fibers
Actions of Autonomic Neurotransmitters
A. Result from binding to protein receptors in the membrane of effector cells:
1. Cholinergic receptors
a. Bind to acetylcholine (Ach)
b. Muscarinic
1.) Excitatory
2.) Slow
c. Nicotinic
1.) Excitatory
2.) Rapid
2. Adrenergic receptors
a. Bind to epinephrine and norepinephrine
b. Alpha and beta
1.) Both elicit different responses on various effectors
Terminating Autonomic Neurotransmitter Actions
A. The enzyme acetylcholinesterase rapidly decomposes the acetylcholine that
cholinergic fibers release.
B. Norepinephrine from adrenergic fibers is removed by active transport.
Control of Autonomic Activity
A. Controlled largely by CNS
B. Medulla oblongata regulates cardiac, vasomotor and respiratory activities
C. Hypothalamus regulates visceral functions, such as body temperature, hunger,
thirst, and water and electrolyte balance
D. Limbic system and cerebral cortex control emotional responses
11.8: Lifespan Changes
A. Brain cells begin to die before birth
B. Over average lifetime, brain shrinks 10%
C. Most cell death occurs in temporal lobes
D. By age 90, frontal cortex has lost half its neurons
E. Number of dendritic branches decreases
F. Decreased levels of neurotransmitters
G. Fading memory
H. Slowed responses and reflexes
I. Increased risk of falling
J. Changes in sleep patterns that result in fewer sleeping hours
Outcomes to be Assessed
11.1: Introduction
Describe the general structure of the brain.
Describe the relationship among the brain, brainstem, and spinal cord.
11.2: Meninges
Describe the coverings of the brain and spinal cord.
11.3: Ventricles and Cerebrospinal Fluid
Describe the formation and function of cerebrospinal fluid.
11.4: Spinal Cord
Describe the structure of the spinal cord and its major functions.
Describe a reflex arc.
Describe reflex behavior.
11.5: Brain
Name the major parts of the brain and describe the functions of each.
Distinguish among motor, sensory, association areas of the cerebral cortex.
Explain hemisphere dominance.
Explain stages in memory storage.
Explain the functions of the limbic system and reticular formation.
11.6: Peripheral Nervous System
List the major parts of the peripheral nervous system.
Describe the structure of a peripheral nerve and how its fibers are classified.
Name the cranial nerves and list their major functions.
Explain how spinal nerves are named and their functions
11.7: Autonomic Nervous System
Describe the general characteristics of the autonomic nervous system.
Distinguish between the sympathetic and the parasympathetic divisions of the
autonomic nervous system.
Describe a sympathetic and a parasympathetic nerve pathway.
Explain how the autonomic neurotransmitters differently affect visceral effectors
Visceral Senses
A. Receptors in internal organs
B. Convey information that includes the sense of fullness after eating a meal as
well as the discomfort of intestinal gas and the pain that signals a heart attack
12.4: Special Senses
A. Sensory receptors are within large, complex sensory organs in the head
B. Smell in olfactory organs
C. Taste in taste buds
D. Hearing and equilibrium in ears
E. Sight in eyes
Sense of Smell
A. Olfactory receptors
1. Chemoreceptors
2. Respond to chemicals dissolved in liquids
B. Olfactory organs
1. Contain olfactory receptors and supporting epithelial cells
2. Cover parts of nasal cavity, superior nasal conchae, and a portion of the
nasal septum
Olfactory Nerve Pathways
A. Once olfactory receptors are stimulated, nerve impulses travel through
B. Olfactory nerves to - olfactory bulbs to - olfactory tracts to limbic
system (for emotions) and olfactory cortex (for interpretation)
Olfactory Stimulation
A. Olfactory organs located high in the nasal cavity above the usual pathway of
inhaled air
B. Olfactory receptors undergo sensory adaptation rapidly
C. Sense of smell drops by 50% within a second after stimulation
D. Olfactory code
1. Hypothesis
2. Odor that is stimulated by a distinct set of receptor cells and its
associated receptor proteins
12.2 Clinical Application: Mixed-Up Senses: Synesthesia
Sense of Taste
A. Taste buds
1. Organs of taste
2. Located on papillae of tongue, roof of mouth, linings of cheeks and
walls of pharynx
B. Taste receptors
1. Chemoreceptors
2. Taste cells modified epithelial cells that function as receptors
3. Taste hairs microvilli that protrude from taste cells; sensitive parts of
taste cells
Taste Sensations
A. Four primary taste sensations
1. Sweet stimulated by carbohydrates
2. Sour stimulated by acids
2. Membranous labyrinth
a. Tube within osseous labyrinth
b. Filled with endolymph
B. Three (3) parts of labyrinths:
1. Cochlea
a. Functions in hearing
2. Semicircular canals
a. Functions in equilibrium
3. Vestibule
a. Functions in equilibrium
Cochlea
A. Scala vestibuli
1. Upper compartment
2. Leads from oval window to apex of spiral
3. Part of bony labyrinth
B. Scala tympani
1. Lower compartment
2. Extends from apex of the cochlea to round window
3. Part of bony labyrinth
C. Cochlear duct
1. Portion of membranous labyrinth in cochlea
D. Vestibular membrane
1. Separates cochlear duct from scala vestibuli
E. Basilar membrane
1. Separates cochlear duct from scala tympani
12.4 Clinical Application: Getting a Cochlear Implant
Organ of Corti
A. Group of hearing receptor cells (hair cells)
B. On upper surface of basilar membrane
C. Different frequencies of vibration move different parts of basilar membrane
D. Particular sound frequencies cause hairs of receptor cells to bend
E. Nerve impulse generated
12.5 Clinical Application: Hearing Loss
Sense of Equilibrium
A. Static equilibrium
1. Vestibule
2. Senses position of head when body is not moving
B. Dynamic Equilibrium
1. Semicircular canals
2. Senses rotation and movement of head and body
Vestibule
A. Utricle
1. Communicates with saccule and membranous portion of semicircular
canals
B. Saccule
1. Communicates with cochlear duct
C. Macula
1. Hair cells of utricle and saccule
Macula
A. Responds to changes in head position
B. Bending of hairs results in generation of nerve impulse
Semicircular Canals
A. Three (3) canals at right angles
1. Ampulla
a. Swelling of membranous labyrinth that communicates with the
vestibule
2. Crista ampullaris
a. Sensory organ of ampulla
b. Hair cells and supporting cells
c. Rapid turns of head or body stimulate hair cells
Sense of Sight
A. Visual accessory organs
1. Eyelids
2. Lacrimal apparatus
3. Extrinsic eye muscles
Eyelid
A. Palpebra
B. Composed of four (4) layers:
1. Skin
2. Muscle
3. Connective tissue
4. Conjunctiva
C. Orbicularis oculi closes eyelid
D. Levator palpebrae superioris opens eyelid
E. Tarsal glands secrete oil onto eyelashes
F. Conjunctiva mucous membrane; lines eyelid and covers portion of eyeball
Lacrimal Apparatus
A. Lacrimal gland
1. Lateral to eye
2. Secretes tears
B. Canaliculi
1. Collect tears
C. Lacrimal sac
1. Collects from canaliculi
D. Nasolacrimal duct
1. Collects from lacrimal sac
2. Empties tears into nasal cavity
Extrinsic Eye Muscles
A. Superior rectus
1. Rotates eye up and medially
B. Inferior rectus
1. Rotates eye down and medially
C. Medial rectus
1. Rotates eye medially
D. Lateral rectus
1. Rotates eye laterally
E. Superior oblique
1. Rotates eye down and laterally
F. Inferior oblique
1. Rotates eye up and laterally
Structure of the Eye
A. Hollow
B. Spherical
C. Wall has three (3) layers:
1. Outer fibrous tunic
2. Middle vascular tunic
3. Inner nervous tunic
Outer Tunic
A. Cornea
1. Anterior portion
2. Transparent
3. Light transmission
4. Light refraction
B. Sclera
1. Posterior portion
2. Opaque
3. Protection
Middle Tunic
A. Iris
1. Anterior portion
2. Pigmented
3. Controls light intensity
B. Ciliary body
1. Anterior portion
2. Pigmented
3. Holds lens
4. Moves lens for focusing
C. Choroid coat
1. Provides blood supply
2. Pigments absorb extra light
Anterior Portion of Eye
A. Filled with aqueous humor
Lens
A. Transparent
B. Biconvex
C. Lies behind iris
D. Largely composed of lens fibers
E. Elastic
B. Image focused on retina is upside down and reversed from left to right
Visual Receptors
A. Rods
1. Long, thin projections
2. Contain light sensitive pigment called rhodopsin
3. Hundred times more sensitive to light than cones
4. Provide vision in dim light
5. Produce colorless vision
6. Produce outlines of objects
B. Cones
1. Short, blunt projections
2. Contain light sensitive pigments called erythrolabe, chlorolabe, and
cyanolabe
3. Provide vision in bright light
4. Produce sharp images
5. Produce color vision
12.6 Clinical Application: Refraction Disorders
Visual Pigments
A. Rhodopsin
1. Light-sensitive pigment in rods
2. Decomposes in presence of light
3. Triggers a complex series of reactions that initiate nerve impulses
4. Impulses travel along optic nerve
B. Pigments on cones
1. Each set contains different light-sensitive pigment
2. Each set is sensitive to different wavelengths
3. Color perceived depends on which sets of cones are stimulated
4. Erythrolabe responds to red
5. Chlorolabe responds to green
6. Cyanolabe responds to blue
Stereoscopic Vision
A. Provides perception of distance and depth
B. Results from formation of two slightly different retinal images
12.5: Lifespan Changes
A. Age related hearing loss due to:
1. Damage of hair cells in organ of Corti
2. Degeneration of nerve pathways to the brain
3. Tinnitus
B. Age-related visual problems include:
1. Dry eyes
2. Floaters (crystals in vitreous humor)
3. Loss of elasticity of lens
4. Glaucoma
5. Cataracts
6. Macular degeneration
Outcomes to be Assessed
12.1: Introduction
Explain the difference between general senses and special senses.
12.2: Receptors, Sensation, and Perception
Name the five types of receptors and state the function of each.
Explain how receptors stimulate sensory impulses.
Explain how a sensation is produced.
12.3: General Senses
Distinguish between general and special senses.
Describe the differences among receptors associated with the senses of touch,
pressure, temperature, and pain.
Describe how the sensation of pain is produced.
Explain the importance of stretch receptors in muscles and tendons.
12.4: Special Senses
Explain the relationship between the senses of smell and taste.
Name the parts of the ear and the function of each part.
Distinguish between static and dynamic equilibrium.
Name the parts of the eye and the function of each part.
Explain how the eye refracts light.
Explain how the brain perceives depth and distance.
Draw a diagram of the visual nerve pathways.
A. Steroids
Review Table 13.4
Review Figure 13.5
Animation: Mechanism of Steroid Hormone Action
Action of Hormones
Non-steroid hormones
Review Table 13.5
Review Figure 13.7
Animation: Peptide Hormone Action
13.1 Clinical Application
Prostaglandins
A. Prostaglandins:
1. Are paracrine substances
2. Act locally
3. Are very potent in small amounts
4. Are not stored in cells but synthesized just before release
5. Rapidly inactivate
6. Regulate cellular responses to hormones
7. Can activate or inhibit adenylate cyclase
a. Controls cAMP production
b. Alters a cells response to hormones
8. Has a wide variety of effects
13.4: Control of Hormonal Secretions
A. Primarily controlled by negative feedback mechanism
B. Hormones can be short-lived or may last for days
C. Hormone secretions are precisely regulated
Control Sources
Review Figure 13.10
Control Sources
Review Figure 13.8
13.5: Pituitary Gland
A. Lies at the base of the brain in the sella turcica
B. Consists of two distinct portions:
1. Anterior pituitary (adenohypophysis)
2. Posterior pituitary (neurohypophysis)
Review Figure 13.9
Anterior Pituitary Hormones
A. Hypothalamic releasing hormones stimulate cells of anterior pituitary to
release hormones
B. Nerve impulses from hypothalamus stimulate nerve endings in the posterior
pituitary gland to release hormones
Review Figure 13.12
Review Figures 13.13 and 13.14
Review Figure 13.15
13.2 Clinical Application
Posterior Pituitary Hormones
Outcomes to be Assessed
13.1: Introduction
Define hormone.
Distinguish between endocrine and exocrine glands.
13.2: General Characteristics of the Endocrine System
Explain what makes a cell a target cell for a hormone.
List some important functions of hormones.
13.3: Hormone Action
Describe how hormones can be classified according to their chemical
composition.
Explain how steroid and non-steroid hormones affect their target cells.
13.4: Control of Hormone Secretion
Discuss how negative feedback mechanisms regulate hormone secretion.
Explain how the nervous system controls hormone secretion.
13.5-13.10: Pituitary Gland Other Endocrine Glands
Name and describe the locations of the major endocrine glands and list the
hormones that they secrete.
Describe the actions of the various hormones and their contributions to
homeostasis.
Explain how the secretion of each hormone is regulated.
13.11: Stress and Its Effects
Distinguish between physical and psychological stress.
Describe the general stress response.
13.12: Lifespan Changes
Describe some of the changes associated with aging of the endocrine system.
Plasma Electrolytes
A. Plasma contains a variety of these ions called electrolytes
B. They are absorbed from the intestine or released as by-products of cellular
metabolism
C. They include:
1. Sodium (most abundant with chloride)
2. Potassium
3. Calcium
4. Magnesium
5. Chloride (most abundant with sodium)
6. Bicarbonate
7. Phosphate
8. Sulfate
14.4: Hemostasis
A. Hemostasis refers to the stoppage of bleeding
B. Actions that limit or prevent blood loss include:
1. Blood vessel spasm
2. Platelet plug formation
3. Blood coagulation
Blood Vessel Spasm
A. Blood vessel spasm
1. Triggered by pain receptors, platelet release, or serotonin
2. Smooth muscle in blood vessel contracts
Platelet Plug Formation
A. Platelet plug formation
1. Triggered by exposure of platelets to collagen
2. Platelets adhere to rough surface to form a plug
Review Figure 14.17
Blood Coagulation
A. Blood coagulation
1. Triggered by cellular damage and blood contact with foreign surfaces
2. A blood clot forms
3. This is a:
a. Hemostatic mechanism
b. Causes the formation of a blot clot via a series of reactions which
activates the next in a cascade
c. Occurs extrinsically or intrinsically
Review Table 14.7
Extrinsic Clotting Mechanism
A. Extrinsic clotting mechanism
1. Chemical outside of blood vessel triggers blood coagulation
2. Triggered by tissue thromboplastin (factor III) (not found in blood)
3. A number of events occur that includes factor VII, factor X, factor V,
factor IV, and factor II (prothrombin)
4. Triggered when blood contacts damaged blood vessel walls or tissues
5. This is an example of a positive feedback mechanism
1. Antigen A
2. Antigen B
Review Table 14.12
Review Table 14.13
Rh Blood Group
A. The Rh blood group was named for the rhesus monkey
B. The group includes several Rh antigens or factors
C. Rh positive presence of antigen D or other Rh antigens on the red blood cell
membranes
D. Rh negative lack of these antigens
E. The seriousness of the Rh blood group is evident in a fetus that develops the
condition erythroblastosis fetalis or hemolytic disease of the newborn
Review Figure 14.23
Outcomes to be Assessed
14.1: Introduction
Describe the general characteristics of blood and discuss its major functions.
Distinguish among the formed elements of blood and the liquid portion of blood.
14.2: Blood Cells
Describe the origin of blood cells.
Explain the significance of red blood cells counts and how they are used to
diagnose disease.
Discuss the life cycle of a red blood cell.
Summarize the control of red blood cell production.
Distinguish among the five types of white blood cells and give the function(s) of
each type.
Describe a blood platelet and explain its functions.
14.3: Blood Plasma
Describe the functions of each of the major components of plasma.
14.4: Hemostasis
Define hemostasis and explain the mechanisms that help to achieve it.
Review the major steps in coagulation.
Explain how to prevent coagulation.
14.5: Blood Groups and Transfusions
Explain blood typing and how it is used to avoid adverse reactions following
blood transfusions.
Describe how blood reactions may occur between fetal and maternal tissues.
2. The chordae tendinae prevent the cusps of the valves from bulging too far
into the atria
3. The atria relax
4. The blood flows into atria
5. The ventricular pressure increases and opens the semilunar valves
6. The blood flows into pulmonary trunk and aorta
Animation: The Cardiac Cycle
Animation: Mechanical Events of the Cardiac Cycle
Heart Sounds
A. A heart beat through a stethoscope sounds like lubb-dupp
B. The lubb
1. The first heart sound
2. It occurs during ventricular systole
3. The A-V valves are closing
C. The dupp
1. The second heart sound
2. It occurs during ventricular diastole
3. The pulmonary and aortic semilunar valves are closing
D. A murmur abnormal heart sound from the cusps not completely closing
Review Figure 15.17
Cardiac Muscle Fibers
A. Cardiac muscle fibers form a functional syncytium
B. This is a mass of cells that function as a unit
C. Two such areas exist in the heart:
1. In the atrial walls called the atrial syncytium
2. In the ventricular walls called the ventricular syncytium
Animation: Action Potentials in the Sinoatrial (SA) Node
Cardiac Conduction System
A. Clumps or strands of specialized cardiac muscle tissue which initiate and
distribute impulses throughout the myocardium
B. The cardiac conduction system coordinates the events of the cardiac cycle
Review Figure 15.19
Review Figures 15.18 and 15.20
Animation: Conducting System of the Heart
15.1 From Science to Technology
Electrocardiogram
A. An electrocardiogram or ECG is a recording of electrical changes that occur in
the myocardium during the cardiac cycle
B. It is used to assess the hearts ability to conduct impulses
C. The deflections in the normal ECG, or waves, include:
1. P wave atrial depolarization
2. QRS complex (three waves) ventricular depolarization
3. T wave ventricular repolarization
Animation: Baroreceptor Reflex Control of Blood Pressure
Review Figures 15.21 and 15.23
Review Figure 15.22
A. Blood pressure decreases as the blood moves through the arterial system and
into the capillary network, so little pressure remains at the venular ends of the
capillaries
B. Only partly a direct result of heart action
C. Dependent on:
1. Skeletal muscle contraction
2. Breathing
3. Venoconstriction
Review Figure 15.39
15.5 Clinical Application
Central Venous Pressure
A. All veins, except those returning to the heart from the lungs, drain into the
right atrium
B. This is therefore pressure in the right atrium
C. Factors that influence it alter flow of blood into the right atrium
D. It effects pressure within the peripheral veins
E. A weakly beating heart increases central venous pressure
F. An increase in central venous pressure causes blood to back up into the
peripheral veins
G. This can lead to peripheral edema
15.6 Clinical Application
15.6: Paths of Circulation
A. Blood vessels can be divided into two major pathways:
1. The pulmonary circuit
2. The systemic circuit (includes coronary circulation)
Pulmonary Circuit
Review Figure 15.40
Review Figure 15.41
Systemic Circuit
A. Composed of vessels that lead from the heart to all body parts (except the
lungs) and back to the heart
B. Includes the aorta and its branches
C. Includes the system of veins that return blood to the right atrium
15.7: Arterial System
Review Figure 15.51
Principal Branches of the Aorta
Review Table 15.4
Review Figures 15.42 and 15.43
Arteries to the Brain, Head, and Neck
Review Figures 15.44, 15.45, and 15.46
Arteries to the Shoulder and Upper Limb
Review Figure 15.47
Arteries to the Thoracic and Abdominal Walls
Review Figure 15.48
Arteries to the Pelvis and Lower Limb
Review Figures 15.49 and 15.50
Describe how substances are exchanged between blood in capillaries and the
tissue fluid surrounding body cells.
15.5: Blood Pressure
Explain how blood pressure is produced and controlled.
Describe the mechanisms that aid in returning venous blood to the heart.
15.6: Paths of Circulation
Compare the pulmonary and systemic circuits of the cardiovascular system.
15.7-15.8: Arterial System Venous System
Identify and locate the major arteries and veins.
15.9: Lifespan Changes
Describe the lifespan changes in the cardiovascular system.
A. Filtration from the plasma normally exceeds reabsorption, leading to the net
formation of tissue fluid
B. This increases the tissue fluid hydrostatic pressure within interstitial spaces
forcing fluid into lymphatic capillaries forming lymph
C. This process prevents accumulation of excess tissue fluid or edema
Lymph Function
A. Lymphatic vessels play a role in:
1. Absorption of dietary fats
2. Delivering fats to the bloodstream
3. Collecting of excess interstitial fluids
4. Delivering excess fluids to the bloodstream
5. Delivering foreign particles to the lymph nodes
Review Figure 16.8
16.4: Lymph Movement
A. Hydrostatic pressure of tissue fluid drives the lymph into the lymphatic
capillaries
B. Muscle activity largely influences the movement of lymph through the
lymphatic vessels via:
1. Action of skeletal muscles
2. Respiratory movements
3. Smooth muscle in the larger lymphatic vessels
4. Valves in the lymphatic vessels
Lymph Flow
Review Figure 16.10
Obstruction of Lymph Movement
Review Figure 16.9
16.5: Lymph Nodes
A. Lymph nodes or lymph glands are located along the lymphatic pathways
B. They contain lymphocytes and macrophages to fight invading pathogens
Structure of a Lymph Node
Review Figure 16.10
Locations of Lymph Nodes
A. Lymph nodes are found in groups or chains along the paths of the larger
lymphatic vessels throughout the body, including the:
1. Cervical region
2. Axillary region
3. Supratrochlear region
4. Inguinal region
5. Pelvic cavity
6. Abdominal cavity
7. Thoracic cavity
Review Figure 16.11
Functions of Lymph Nodes
A. Lymph nodes have two primary functions:
1. Filter potentially harmful particles from the lymph
2. Act with immune surveillance provided by macrophages and lymphocytes
B. Along with the red bone marrow, the lymph nodes are centers for lymphocyte
production
16.6: Thymus and Spleen
A. These are two other lymphatic organs with functions similar to those of the
lymph nodes
Thymus
A. The thymus is:
1. Larger in infancy and during puberty
2. Small in an adult
3. Replaced by fat and connective tissue in the elderly
4. Site of T lymphocyte (or T cell) production
5. Secretes protein hormones called thymosins
Review Figure 16.13
Review Figure 16.12
Spleen
A. The spleen is:
1. The largest lymphatic organ
2. Located in the upper left abdominal quadrant
3. Has sinuses filled with blood
4. Contains two tissue types:
a. White pulp (lymphocytes)
b. Red pulp (red blood cells, lymphocytes and macrophages)
Review Figure 16.14
Review Table 16.1
16.7: Body Defenses Against Infection
A. The presence and multiplication of a pathogen in the body may cause an
infection
B. Pathogens are:
1. Disease causing agents
2. Bacteria, viruses, complex microorganisms, and spores of multicellular
organisms
C. The body can prevent entry of pathogens or destroy them with defense
mechanisms such as:
1. Innate defenses:
a. These are general defenses
b. They protect against many pathogens
2. Adaptive defenses:
a. Known as immunity
b. More specific and precise targeting specific antigens
c. Are carried out by lymphocytes
16.8: Innate (Nonspecific) Defenses
Review Table 16.3
Species Resistance
A. Refers to a given type of organism, or species, that develops diseases unique to
it
Animation: Nonspecific Immunity
Mechanical Barriers
A. The skin and mucous membranes create mechanical barriers
B. Mechanical barriers are considered the first line of defense (all other nonspecific defenses are part of the second line of defense)
Chemical Barriers
A. Enzymes in body fluids provide a chemical barrier to pathogens, and they may
include:
1. Interferons are hormone-like peptides and stimulate phagocytosis
2. Defensins are peptides produced by neutrophils and other granulocytes.
They cripple microbes.
3. Collectins are proteins with broad protection against bacteria, yeast and
some viruses
4. Complement is a group of proteins in plasma and other body fluids that
stimulate inflammation, attract phagocytes and enhance phagocytosis
Animation: Antiviral Activity of Interferon
Animation: Activation of Complement
Animation: Complement Function
Natural Killer (NK) Cells
A. NK cells are a small population of lymphocytes defending against viruses and
cancer by secreting cytolytic substances called perforins that destroy the infected
cell
B. NK may also enhance inflammation
Inflammation
A. Inflammation produces local redness, swelling, heat and pain
B. Table 16.2 summarizes the process
Animation: The Inflammatory Responses
Phagocytosis
A. Phagocytosis removes foreign particles from the lymph
B. Phagocytes are also in the blood vessels and in the tissues of the spleen, liver
or bone marrow
C. The most active phagocytic cells are neutrophils and monocytes
D. Chemicals attract these phagocytic cells to the injury and this is called
chemotaxis
Animation: Phagocytosis
Fever
A. A fever begins when a viral or bacterial infection stimulates lymphocytes to
proliferate, producing cells that secrete a substance called interleukin-1 (IL-1)
16.9: Adaptive (Specific) Defenses or Immunity
A. This is the third line of defense and known as immunity
B. It is resistance to particular pathogens or to their toxins or metabolic byproducts
C. It is based on the ability to distinguish molecules that are part of the body
(self from non-self)
D. Antigens are molecules that can elicit an immune response
Antigens
A. Antigens may be:
1. Proteins
2. Polysaccharides
3. Glycoproteins
4. Glycolipids
B. The most effective antigens are large and complex
C. Haptens are small molecules that are not antigenic by themselves, but when
they combine with a large molecule can stimulate an immune response
Lymphocyte Origins
Review Figure 16.16
T Cells and the Cellular Immune Response
A. A lymphocyte must be activated before it can respond to an antigen
B. T cell activation requires antigen-presenting cell (accessory cell) and may
include macrophages, B cells and several other types of cells
C. Requires major histocompatibility complex (MHC) or human leukocyte
antigens (HLA) to recognize non-self
D. T cells can synthesize and secrete polypeptides called cytokines
E. Types of specialized T cells include:
1. Helper T cells
2. Cytotoxic T cells
3. Memory T cells
Animation: Cytotoxic T-cell Activity Against Target Cells
Animation: Interaction of Antigen Presenting Cells and T-helper Cells
Review Table 16.5
B Cells and the Humoral Immune Response
A. B cells can be activated when an antigen fits the shape of its receptor
B. Most of the time B cell activation requires T cells
C. T cells release cytokines that stimulate B cells
D. Some B cells may become memory B cells while others differentiate into
plasma cells and produce and secrete large globular proteins called antibodies or
immunoglobulins
Review Figure 16.17
Review Figure 16.18
Review Figure 16.19
Review Table 16.6
Animation: Monoclonal Antibody Production
Review Tables 16.7 and 16.8
Animation: Antibodies
16.1 From Science to Technology
Immune Responses
Review Figure 16.21
Animation: The Immune Response
Practical Classification of Immunity
Review Table 16.9
Allergic Reactions
A. Type I
1. Immediate-reaction allergy
F. Elderly may not be candidates for certain medical treatments that suppresses
immunity
16.1 Clinical Application
Outcomes to be Assessed
16.1: Introduction
Describe the general functions of the lymphatic system.
16.2: Lymphatic Pathways
Identify and describe the parts of the major lymphatic pathways.
16.3: Tissue Fluid and Lymph
Describe how tissue fluid and lymph form, and explain the function of lymph.
16.4: Lymph Movement
Explain how lymphatic circulation is maintained, and describe the consequence
of lymphatic obstruction.
16.5: Lymph Nodes
Describe a lymph node and its major functions.
Describe the location of the major chains of lymph nodes.
16.6: Thymus and Spleen
Discuss the locations and functions of the thymus and spleen.
16.7: Body Defenses Against Infection
Distinguish between innate (nonspecific) and adaptive (specific) defenses.
16.8: Innate (Nonspecific) Defenses
List seven innate body defense mechanisms, and describe the action of each
mechanism.
16.9: Adaptive (Specific) Defenses, or Immunity
Explain how two major types of lymphocytes are formed, activated, and how
they function in immune mechanisms.
Discuss the origins and actions of the five different types of antibodies.
Distinguish between primary and secondary immune responses.
Distinguish between active and passive immunity.
Explain how allergic reactions, tissue rejection reactions, and autoimmunity arise
from immune mechanisms.
16.10: Lifespan Changes
Describe lifespan changes in immunity.
Palate
A. The palate forms the roof of the oral cavity and consists of a hard anterior part
and a soft posterior part
Review Figure 17.7
Teeth
A. The teeth are the hardest structures in the body
B. There are primary (deciduous) teeth numbering 20
C. There are secondary (permanent) teeth numbering 32
Review Figure 17.8
Review Table 17.2 and Figure 17.9
Review Figure 17.10
17.1 Clinical Application
17.4: Salivary Glands
A. Salivary glands secrete saliva
B. This begins the digestion of carbohydrates
C. There are three pairs of major salivary glands, including:
1. Parotid glands
2. Submandibular glands
3. Sublingual glands
D. There are many minor glands scattered throughout the mucosa of the tongue,
palate, and cheeks
Salivary Secretions
A. The different salivary glands have varying proportions of two types of
secretory cells, serous cells and mucous cells
1. Serous cells produce a watery fluid with a digestive enzyme called salivary
amylase
2. Mucous cells secrete mucous
B. Parotid glands
1. Secrete clear watery, serous fluid
2. Rich in salivary amylase
C. Submandibular glands
1. Secrete primarily serous fluid and some mucus
D. Sublingual glands
1. Secrete primarily mucus
Major Salivary Glands
Review Figures 17.11 and 17.12
17.5: Pharynx and Esophagus
A. The pharynx is a cavity posterior to the mouth from which the tubular
esophagus leads to the stomach
B. Both the pharynx and esophagus muscular walls function in swallowing
Review Figure 17.13
Structure of the Pharynx
A. The pharynx can be divided into the following parts:
1. Nasopharynx
2. Oropharynx
3. Laryngopharynx
1. Phenol
2. Hydrogen sulfide
3. Indole
4. Skatole
5. Ammonia
17.5 Clinical Application
17.11: Lifespan Changes
A. Changes to the digestive system are slow and slight, and eventually include:
1. Teeth may become sensitive
2. Gums may recede
3. Teeth may loosen, break or fall out
4. Heartburn may become more frequent
5. Constipation may become more frequent
6. Nutrient absorption decreases
7. Accessory organs age but typically not necessarily in ways that effect
health
Outcomes to be Assessed
17.1: Introduction
Describe the general functions of the digestive system.
Name the major organs of the digestive system.
17.2: General Characteristics of the Alimentary Canal
Describe the structure of the wall of the alimentary canal.
Explain how the contents of the alimentary canal are mixed and moved.
17.3: Mouth
Describe the functions of the structures of the mouth.
Describe how different types of teeth are adapted for different functions, and list
the parts of the tooth.
17.4-17.10: Salivary Glands Large Intestine
Locate each of the organs and glands; then describe the general function of each.
Identify the function of each enzyme secreted by the digestive organs and glands.
Describe how digestive secretions are regulated.
Explain control of movement of material through the alimentary canal.
Describe the mechanisms of swallowing, vomiting, and defecating.
Explain how the products of digestion are absorbed.
17.11: Lifespan Changes
Describe aging-related changes in the digestive system.
B. Requirements vary with age, sex, growth rate, level of physical activity and
stress, and genetic and environmental factors
C. Dietary requirements such as recommended daily allowances (RDA) are best
to follow
D. The U.S. Department of Agricultures Food Pyramid is another tool to follow
E. Nutritional information and ingredients are listed on most grocery items for
retail sale
Review Figure 18.20
Malnutrition
A. Malnutrition is poor nutrition that results from a lack of essential nutrients or
failure to use them
1. Undernutrition deficiency of essential nutrients
2. Overnutrition excess of nutrient intake
B. Malnutrition can be a result of:
1. Primary malnutrition malnutrition from diet alone
2. Secondary malnutrition adequate diet but individual characteristics make
the diet insufficient
18.2 Clinical Application
Starvation
A. A healthy human can survive 50-70 days without food
B. Symptoms include low blood pressure, slow pulse, chills, dry skin, hair loss,
and poor immunity
C. Common nutritional disorders include:
1. Marasmus lack of all nutrients
2. Kwashiorkor protein starvation
3. Anorexia nervosa eating disorder; self-starvation
4. Bulimia eating disorder; binge and purge cycle
18.3 Clinical Application
18.9: Lifespan Changes
A. Dietary requirements remain generally the same throughout life
B. BMR rises in early childhood and peaks in adolescence
C. BMR declines in adulthood
D. Change in nutrition often reflects the effects of medical conditions and the
social and economic circumstances
Review Table 18.12
Outcomes to be Assessed
18.1: Introduction
Define nutrition, nutrients, and essential nutrients.
Explain appetite control.
18.2-18.4: Carbohydrate - Proteins
List the major sources of carbohydrates, lipids, and proteins.
Describe how cells utilize carbohydrates, lipids, and proteins.
Define nitrogen balance.
18.5: Energy Expenditures
Explain how energy values of food are determined.
Explain the factors that affect an individuals energy requirements.
Pharynx
A. The pharynx is posterior to the oral cavity and between the nasal cavity and the
larynx
Review Figure 19.2
Larynx
A. The larynx is an enlargement in the airway superior to the trachea and inferior
to the pharynx
B. It is composed of a framework of muscles and cartilages bound by elastic
tissue
Review Figures 19.5, 19.6, and 19.7
Trachea
A. The trachea (windpipe) is a flexible cylindrical tube about 2.5 centimeters in
diameter and 12.5 centimeters in length
B. As it extends downward anterior to the esophagus and into the thoracic cavity,
it splits into the right and left primary bronchi
Review Figure 19.8
Review Figures 19.9, 19.10, and 19.11
Bronchial Tree
A. The bronchial tree consists of branched airways leading from the trachea to the
microscopic air sacs in the lungs
Review Figure 19.12
Branches of the Bronchial Tree
A. The successive divisions of the branches from the trachea to the alveoli are:
1. Right and left primary bronchi
2. Secondary or lobar bronchi
3. Tertiary or segmental bronchi
4. Intralobular bronchioles
5. Terminal bronchioles
6. Respiratory bronchioles
7. Alveolar ducts
8. Alveolar sacs
9. Alveoli
Review Figure 19.13
Review Figures 19.14 and 19.15
The Respiratory Tubes
A. The structure of the bronchus is similar to that of the trachea, but the C-shaped
cartilaginous rings are replaced with cartilaginous plates where the bronchus
enters the lung
B. These respiratory tubes become thinner and thinner, and the cell layers thin and
change until the alveoli is reached
C. It is the alveoli that provides surface area for gas exchange
Review Figure 19.16
Review Figures 19.17 and 19.18
Animation: Alveolar Pressure Changes During Inspiration and Expiration
Lungs
A. The right and left lungs are soft, spongy, cone-shaped organs in the thoracic
cavity
B. The right lung has three lobes and the left lung two lobes
Review Figures 19.19 and 19.20
Animation: The Pleural Membranes
Review Table 19.1
19.2 Clinical Application
19.4: Breathing Mechanism
A. Breathing or ventilation is the movement of air from outside of the body into
the bronchial tree and the alveoli
B. The actions responsible for these air movements are inspiration, or inhalation,
and expiration, or exhalation
Inspiration
A. Atmospheric pressure due to the weight of the air is the force that moves air
into the lungs
B. At sea level, atmospheric pressure is 760 millimeters of mercury (mm Hg)
C. Moving the plunger of a syringe causes air to move in or out
D. Air movements in and out of the lungs occur in much the same way
Review Figures 19.21 and 19.22
Inspiration
A. Intra-alveolar pressure decreases to about 758mm Hg as the thoracic cavity
enlarges due to diaphragm downward movement caused by impulses carried by
the phrenic nerves
B. Atmospheric pressure then forces air into the airways
Review Figure 19.23
Inspiration
Review Figure 19.24
Review Table 19.2
Expiration
A. The forces responsible for normal resting expiration come from elastic recoil
of lung tissues and from surface tension
B. These factors increase the intra-alveolar pressure about 1 mm Hg above
atmospheric pressure forcing air out of the lungs
Expiration
Review Figure 19.25
Review Table 19.3
Respiratory Air Volumes and Capacities
A. Different degrees of effort in breathing move different volumes of air in and
out of the lungs
B. This measurement of volumes is called spirometry
Review Figure 19.26
Review Table 19.4
Alveolar Ventilation
A. The volume of new atmospheric air moved into the respiratory passages each
minute is minute ventilation
B. It equals the tidal volume multiplied by the breathing rate
C. Much of the new air remains in the physiologic dead space
D. The tidal volume minus the physiologic dead space then multiplied by
breathing rate is the alveolar ventilation rate
A. The alveoli are the sites of the vital process of gas exchange between the air
and the blood
Alveoli
Review Figure 19.32
Review Figure 19.33
Respiratory Membrane
A. Part of the wall of an alveolus is made up of cells (type II cells) that secrete
pulmonary surfactant
B. The bulk of the wall of an alveolus consists of a layer of simple squamous
epithelium (type I cells)
C. Both of these layers make up the respiratory membrane through which gas
exchange takes place
Review Figure 19.34
Review Figure 19.35
Animation: Gas Exchange During Respiration
Diffusion Through the Respiratory Membrane
A. Molecules diffuse from regions where they are in higher concentration toward
regions where they are in lower concentration
B. It is important to know the concentration gradient
C. In respiration, think in terms of gas partial pressures
D. Gases diffuse from areas of higher partial pressure to areas of lower partial
pressure
E. The respiratory membrane is normally thin and gas exchange is rapid
1. Increased diffusion is favored with more surface area, shorter distance,
greater solubility of gases and a steeper partial pressure gradient
2. Decreased diffusion occurs from decreased surface area
19.5 Clinical Application
19.6 Clinical Application
19.7: Gas Transport
A. Blood transports O2 and CO2 between the lungs and the body cells
B. As the gases enter the blood, they dissolve in the plasma or chemically
combine with other atoms or molecules
Oxygen Transport
A. Almost all oxygen carried in the blood is bound to the protein hemoglobin in
the form of oxyhemoglobin
B. Chemical bonds between O2 and hemoglobin are relatively unstable
C. Oxyhemoglobin releases O2 into the body cells
D. About 75% of the O2 remains bound to hemoglobin in the venous blood
ensuring safe CO2 levels and thereby pH
Review Figure 19.37
Review Figure 19.36
Review Figures 19.38, 19.39, and 19.40
Carbon Dioxide Transport
A. Blood flowing through capillaries gains CO2 because the tissues have a high
Pco2
B. The CO2 is transported to the lungs in one of three forms:
1. As CO2 dissolved in plasma
1. Substances move from the renal tubules into the interstitial fluid where
they then diffuse into the peritubular capillaries
2. The proximal convoluted tubule reabsorbs (70%):
a. Glucose, water, urea, proteins, and creatine
b. Amino, lactic, citric, and uric acids
c. Phosphate, sulfate, calcium, potassium, and sodium ions
Review Figure 20.21
Review Figure 20.22
Review Table 20.2
20.3 Clinical Application
Tubular Secretion
A. Tubular secretion
1. Substances move from the plasma of the peritubular capillaries into the
fluid of the renal tubules
2. Active transport mechanisms function here
3. Secretion of substances such as drugs and ions
Review Figure 20.23
Regulation of Urine Concentration and Volume
A. Hormones such as aldosterone and ANP affect the solute concentration of
urine, particularly sodium
B. The ability of the kidneys to maintain the internal environment rests in a large
part on their ability to concentrate urine by reabsorbing large volumes of water
C. The distal convoluted tubule and the collecting duct are impermeable to water,
so water may be excreted as dilute urine
D. If ADH is present, these segments become permeable, and water is reabsorbed
by osmosis into the extremely hypertonic medullary interstitial fluid
E. A countercurrent mechanism in the nephron loops (the descending and the
ascending limbs) ensures that the medullary interstitial fluid becomes hypertonic
F. This mechanism is known as the countercurrent multiplier
G. The vasa recta also contributes as a countercurrent mechanism
Review Figure 20.24
Review Table 20.3
Review Figure 20.25
Review Figure 20.26
Review Table 20.4
Urea and Uric Acid Excretion
A. Urea:
1. A by-product of amino acid catabolism
2. The plasma concentration reflects the amount or protein in diet
3. It enters the renal tubules through glomerular filtration
4. It contributes to the reabsorption of water from the collecting duct
5. About 80% is recycled
B. Uric acid:
1. Is a product of nucleic acid metabolism
2. It enters the renal tubules through glomerular filtration
3. Most reabsorption occurs by active transport
B. It contacts the anterior walls of the uterus and vagina in the female, and lies
posteriorly against the rectum in the male
C. The openings for the ureters is the area of trigone
D. It has four layers: inner mucous coat, a submucous coat, a muscular coat, and
an outer serous coat
E. Smooth muscle fibers comprise the detrusor muscle which is the muscle of the
bladder wall
Review Figure 20.28
Review Figure 20.29
Review Figure 20.30
Review Figure 20.32
Urethra
A. The urethra is a tube that conveys urine from the urinary bladder to the outside
of the body
B. Its wall is lined with a mucous membrane and it has a thick layer of
longitudinal smooth muscle fibers
C. In a female:
1. It is about 4 centimeters long
2. It runs obliquely
D. In a male:
1. It is about 17.5 centimeters long
2. It has a dual function for both urination and reproduction
3. It has three sections:
a. Prostatic urethra
b. Membranous urethra
c. Penile urethra
Review Figure 20.31
Micturition
A. Urine leaves the urinary bladder by micturition or urination reflex
Review Table 20.5
Animation: Micturition Reflex
Micturition
Review Table 20.6
Animation: Renal Process
20.4 Clinical Application
20.5: Lifespan Changes
A. The urinary system is sufficiently redundant, in both structure and function, to
mask age-related changes
B. The kidneys become slower to remove nitrogenous wastes and toxins and to
compensate for changes that maintain homeostasis
C. Changes include:
1. The kidneys appear scarred and grainy
2. Kidney cells die
3. By age 80 the kidneys have lost a third of their mass
4. Kidney shrinkage is due to loss of glomeruli
5. Proteinuria may develop
Explain how chemical buffer systems, the respiratory system, and the kidneys
keep the pH of body fluids relatively constant.
21.6: Acid-Base Imbalances
Describe the causes and consequences of increase or decrease in body fluid pH.
A. The fluid the urethra conveys to the outside during ejaculation is called semen
B. Semen consists of:
1. Sperm cells
2. Secretions of the seminal vesicles, prostate gland, and bulbourethral glands
3. It is slightly alkaline
4. Contains prostaglandins
5. Contains nutrients
6. Volume is 2-5 milliliters of semen per ejaculation
7. Average 120 million sperm cells per milliliter of semen
22.1 Clinical Application
22.2 Clinical Application
Male External Reproductive Organs
A. Includes the:
1. Scrotum (and two testes)
2. Penis
Review Figure 22.4
Scrotum
A. Pouch of skin and subcutaneous tissue
B. Dartos muscle smooth muscle in subcutaneous tissue; contracts to cause
wrinkling of the scrotum
C. Medial septum divides the scrotum into two chambers
D. Each chamber is lined with a serous membrane
E. Each chamber houses a testis and epididymis
Penis
A. Conveys urine and semen
B. Specialized to become erect for insertion into the vagina
Review Figure 22.15
Erection, Orgasm, and Ejaculation
A. The erection:
1. Parasympathetic nerve impulses
2. Blood accumulates in the erectile tissues
B. The orgasm:
1. Culmination of sexual stimulation
2. Accompanied by emission and ejaculation
C. The ejaculation:
1. Emission is the movement of semen into the urethra
2. Ejaculation is the movement of semen out of the urethra
3. This is largely dependent on sympathetic nerve impulses
Erection, Orgasm, and Ejaculation
Review Figures 22.16 and 22.17
Review Table 22.1
22.3: Hormonal Control of Male Reproductive Functions
A. Hormones secreted by the hypothalamus, the anterior pituitary gland, and the
testes control male reproductive functions
B. Hormones initiate and maintain sperm cell production and oversee the
development and maintenance of male sex characteristics
Describe fertilization.
23.3: Prenatal Period
List and provide details of the major events of cleavage.
Describe implantation.
Discuss the hormonal and other changes in the maternal body during pregnancy.
Explain how the primary germ layers originate and list the structures each layer
produces.
Describe the major events of the embryonic stage of development.
Describe the formation and function of the placenta.
Define fetus, and describe the major events that occur during the fetal stage of
development.
Trace the path of blood through the fetal cardiovascular system.
Explain the role of hormones in the birth process and milk production.
23.4: Postnatal Period
Describe the major cardiovascular and physiological adjustments that occur in a
newborn.
Name the postnatal stages of development of a human, and indicate the general
characteristics of each stage.
23.5: Aging
Distinguish between active and passive aging.
Contrast lifespan and life expectancy.
B. Polygenic traits
1. Determined by more than one gene
2. Examples include height, skin color, and eye color
C. Multifactorial traits
1. Traits molded by one or more genes plus environmental factors
2. Examples include height and skin color
3. Common diseases such as heart disease, diabetes mellitus, hypertension,
and cancers are multifactorial
Review Figures 24.7, 24.8, and 24.9
24.5: Matters of Sex
A. Human somatic (nonsex) cells include an X and a Y chromosome in males and
two X chromosomes in females
1. All eggs carry a single X chromosome
2. Sperm carry either an X or Y chromosome
B. Sex is determined at conception: a Y-bearing sperm fertilizing an egg
conceives a male, and an X-bearing sperm conceives a female
Review Figure 24.10
Sex Determination
A. Maleness derives from a Y chromosome gene called SRY
B. The SRY gene encodes a type of protein called a transcription factor
C. The SRY activates transcription of genes that direct development of male
structures in the embryo, while suppressing formation of female structures
Review Figure 24.11
Genes of the Sex Chromosomes
A. X chromosome
1. Has over 1,500 genes
2. Most genes on the X chromosome do not have corresponding alleles on the
Y chromosome
B. Y chromosome
1. Has only 231 protein-encoding genes
2. Some genes are unique only to the Y chromosome
Hemophilia
A. Passed from mother (heterozygote) to son
B. Each son has a 50% chance of receiving the recessive allele from the mother
C. Each son with one recessive allele will have the disease
D. Each son has no allele on the Y chromosome to mask the recessive allele
E. Each daughter has a 50% chance of receiving the recessive allele from the
mother
F. Each daughter with one recessive allele will be a carrier
G. Each daughter with one recessive allele does not develop the disease because
she has another X chromosome with a dominant allele
Gender Effects on Phenotype
A. Sex-limited trait
1. Affects a structure or function of the body that is present in only males or
only females
2. Examples are beards or growth of breasts
B. Sex-influenced inheritance
1. An allele is dominant in one sex and recessive in the other
2. Baldness is an example
3. Heterozygous males are bald but heterozygous females are not
24.6: Chromosome Disorders
A. Deviations from the normal chromosome number of 46 produce syndromes
because of the excess or deficit of genes
B. Chromosome number abnormalities may involve single chromosomes or entire
sets of chromosomes
C. Euploid is a normal chromosome number
Polyploidy
A. Polyploidy
1. The most drastic upset in chromosome number
2. This is an entire extra set of chromosomes
3. Results from formation of a diploid, rather than a normal haploid, gamete
4. Most embryos or fetuses die, but occasionally an infant survives a few days
with many abnormalities
Aneuploidy
A. Aneuploidy
1. Cells missing a chromosome or having an extra chromosome
2. Results from meiotic error called nondisjunction
3. Here a chromosome pair fails to separate, either at the first or at the second
meiotic division, producing a sperm or egg that has two copies of a particular
chromosome or none, rather than the normal one copy
4. When a gamete fuses with its mate at fertilization, the resulting zygote has
either 47 or 45 chromosomes, instead of 46
5. Trisomy is the condition of having an extra chromosome
6. Monosomy is the condition of missing a chromosome
Review Table 24.1
24.2 Clinical Application
Prenatal Tests Detect Chromosome Abnormalities
Review Figure 24.13
Review Figure 24.14
Review Table 24.2
24.7: Gene Expression Explains Aspects of Anatomy and Physiology
A. Gene expression patterns can add to what we know about structure and
function of the human body
B. Identifying which genes are active and inactive in particular cell types, under
particular conditions, can add to our understanding of physiology
C. Gene expression monitors the proteins that a cell produces
D. The technology used is termed gene expression profiling, and identifying the
sets of proteins in a cell is proteomics
E. DNA microarrays or DNA chips profile gene expression
F. This is valuable in anatomy and physiology when it allows medical researchers
see distinctions their eyes cannot detect
Review Figure 24.15
Outcomes to be Assessed
24.1: Introduction
Distinguish among genome, gene, and chromosome.
Define genetics.
Explain how genetic information passes from generation to generation.
Explain how the human genome is an economical storehouse of information.
24.2: Modes of Inheritance
State the two bases of genetic predictions.
Define the two types of chromosomes.
Explain the basis of multiple alleles of a gene.
Distinguish between heterozygous and homozygous; genotype and phenotype;
dominant and recessive.
Distinguish between autosomal recessive and autosomal dominant inheritance.
24.3: Factors That Affect Expression of Single Genes
Explain how and why the same genotype can have different phenotypes among
individuals.
24.4: Multifactorial Traits
Describe how traits determined by genes and the environment are inherited.
24.5: Matters of Sex
Describe how and when sex is determined.
Explain how X-linked inheritance differs from inheritance of autosomal traits.
Discuss factors that affect how phenotypes may differ between the sexes.
24.6: Chromosome Disorders
Describe three ways that chromosomes can be abnormal.
Explain how prenatal tests provide information about chromosomes.
24.7: Gene Expression Explains Aspects of Anatomy and Physiology
What type of information does gene expression profiling provide?
Explain how a DNA microarray works.