Documente Academic
Documente Profesional
Documente Cultură
S2, 2014
Lecture Schedule
Code and Title
Lecture Summary
-General Introduction
-Nomenclature
U5L1: Anatomy of the Upper -Oral Cavity
Digestive Tract
-Pharynx
-Oesophagus
-Stomach
Learning Outcomes
Lecturer
With regard to the macroscopic structure of the upper digestive Richard Ward
tract:
ANAT
-Define the various parts of the digestive tract and their individual
boundaries.
-Give a general account of the similarities found along the gut
tube including its nerve and vascular supply.
-Describe and correlate with function the structure of the oral
cavity, orophaynx and laryngopharynx.
-Describe and correlate with function the individual
characteristics and topographical relationships of the
oesophagus and stomach including their nerve and vascular
supply.
-Draw a neat, clearly labelled, identified and orientated diagram
of a sagittal section through the oral cavity, oropharynx and
laryngopharynx.
-Draw a neat, clearly labelled, identified and orientated diagram
of an anterior view of the oesophagus and stomach.
-Tabulate the material used in any description or discussion.
Suz. Ollerenshaw
HSTO
-Know the common wall layers of the GIT.
-Describe the structure and ultrastructure of the upper GIT.
-Identify key features and how they reflect the function of the
organ.
-Classify the epithelium in each region of the upper GIT
Lecture Schedule
Lecture Summary
Learning Outcomes
S2, 2014
Lecturer
Sharon Herkes
PHSI
Sharon Herkes
PHSI
Richard Ward
ANAT
Suz. Ollerenshaw
HSTO
Gareth Denyer
BCHM
U5L17: Molecular
mechanisms &
consequences of diabetes
Lecture Schedule
Lecture Summary
The oral route is the most common way of getting
a pharmaceutical agent into plasma. However,
crossing the gut wall is not straightforward. This
lecture introduces the mechanisms involved in the
passage of drugs from the GIT to the plasma. The
principal pharmacokinetic parameters, AUC, t1/2,
C and V are also introduced.
This lecture outlines phase 1 metabolism, its
characteristics and some key examples. The
importance of phase I metabolism and the effect of
genetic differences in phase I enzyme phenotype
will be exemplified.
This lecture introduces phase II drug metabolism
and provides contextual examples of the effect on
drug elimination and enterohepatic recycling
This final lecture links the previous concepts of
metabolism to their inherent goal which is
elimination of xenobiotica (and drugs). Ways in
which elimination can be altered in the context of
poisoning will be presented.
The gut and its microbes.
Gut anatomy and location of microbes
Infectious diseases of the gut (Bacteria: Enterics,
V. cholera, Campylobacter), Viruses
(enteroviruses), Protists (Giardia, Cryptosporidium,
Entamoeba)
Diarrhoea and infant mortality
Germ-free vs conventional
The concept of the gut microbiota as an
additional organ
Dominant microbes normally found in the gut
(Bacteroidetes and Firmicutes)
Gut pathogens: diarrhoea and ulcers.
Defenses bile salts, mucin
Defenses normal flora
Endogenous vs foodborne acquisition
Toxin-based diseases
Host manipulation (remodeling of cytoskeleton,
expression)
Gut dysbiosis: IBD, obesity and diabetes .
Our microbes cause variation between us
Homeostasis and individuality
Immune state and disease predisposition
influenced by bacteria
Fusobacterium and CD
PRR and inflammation
Learning Outcomes
S2, 2014
Lecturer
Michael Murray
PCOL
Michael Murray
PCOL
Michael Murray
PCOL
Michael Murray
PCOL
Andrew Holmes
MICR
-Know the major pathogens of the gut and the
infection route.
-Know the major barriers to infection by the oral route
-List key anatomical, immunological, and metabolic
differences between GF and conventional gut.
-Know the numerically dominant phyla of the gut
microbiota.
Andrew Holmes
MICR
Andrew Holmes
MICR