Documente Academic
Documente Profesional
Documente Cultură
Definition of pain
IASP 1979 Pain is an unpleasant sensory and emotional experience associated with actual or potential tissue damage or described in terms of such damage.
Definition of terms: Nociception: Neural response to a noxious stimuli. Noxious stimulus: Tissue damaging or potentially damaging stimulus Antinociception: Blockage of nociception
Sensations: Protopathic(noxiuous) Epicritic(nonnoxious).
Classification of Pain
According to duration
Acute pain and chronic pain
According to Etiology
Post-operative pain and Cancer pain
4 distinct process
Transduction : noxious stimuli causes generation of electrical activity in sensory nerve endings. Transmission: impulse CNS. Modulation Perception
Pain Pathway
The sensory information from the somatic segments enters the spinal cord through dorsal roots of spinal nerves. From the spinal cord to the brain, sensory signals are carried through one of the two alternative sensory pathways. 1. The dorsal column-medial lemniscal system. 2. The antero-lateral system-which transmit sensation of pain, thermal sensation, and crude touch.
PAIN RECEPTORS
Are naked, afferent nerve endings of myelinated A and unmyleinated C fibers that encode the occurrence, intensity duration and location of noxious stimuli.
2 types of fibers: small myelinated A 2-5 06-30m/s Sharp, fast, well localized pain.
Unmyelinated C fibers. 0.4-1.2m 0.5-2m/sec Dull, slow, poorly localized.
Pain fibers from head and neck Trigeminal(V): Gasserian ganglion. Facial(VII): Geniculate ganglion. Glossopharyngeal(IX): Superior petrosal. Vagal(X): Jugular ganglion, ganglion nodosum.
Proximal axonal processes of first order neurons in these ganglia reach the brain stem via respective cranial nerves, where they synapse with second order neurons.
Either nociceptive specific or wide dynamic range(WDR). Nociceptive specific serve only noxious stimulus. Arranged in lamina I, normally silent respond to high threshold noxious stimulus. WDR neurons receive non noxious stimuli and from A, A, C fibers. Arranged in mainly in lamina V.
Lamina
Lamina
Input A , C C, A
I II
III
IV V VI VII VIII IX X
Somatic mechanoreception
Mechanoreception Visceral & somatic nociception Mechanoreception Sympathetic
A, A
A, A A, A A
Nucleus proprius
Nucleus proprius Nucleus proprius Nucleus proprius Intermediolateral coloum
A Motor A A
Spinothalamic tract
Main pain pathway.
Physiology of nociception
Nociceptors:
high threshold for activation. Delayed adaptation, sensitization & afterdischarges. Two types of ion channels VR1, VRL-1. Both responds to high temperature, bradykinin, histamine, serotonin, H+, K, prostaglandins, ATP .
Visceral Pain
Mechanism underlying visceral pain include peritoneal inflammation, visceral distension and exaggerated smooth muscle contraction. Smooth muscle contraction is increased by adrenergic sympathetic and cholinergic parasympathetic innervations.
Neurotransmitter
Substance P
Calcitonin Glutamate Aspartate ATP Somatostatin
Receptor
NK 1
NMDA, AMPA NMDA, AMPA P1, P 2
Effect
Excitatory
Excitatory Excitatory Excitatory Excitatory Inhibitory
Acetylcholine
Encephalins Norepinephrine Serotonin
Muscarinic
,,. 2 5-HT
Inhibitory
Inhibitory Inhibitory Inhibitory
GABA
A, B
Inhibitory
Modulation of pain
May occur at nociceptor, spinal cord or in supraspinal structures, can either inhibit or facilitate pain. Peripheral modulation Central modulation
Peripheral modulation
Sensitization of nociceptors by potassium ion and ATP released by tissue trauma and cell destruction. Neuropeptides and amino acids (substance P, Bradykinin, Histamine) trigger inflammation response and sensitize nociceptors and cause hyperalgesia. Spread of hyperalgesia away from the site by antidromal propogation of signals along peripheral branches of sensory nerve and release of substance P vasodilatation release of neuropeptides and amino acids in the surrounding tissue.
Central modulation
Repetitive afferent activation of A delta and C fibers leads to altered characteristics in spinal cord dorsal horn neurons. Changes sensitization, wind up, expansion of receptive field and enhancement of spinal reflexes. Mechanism:- release of excitatory neurotransmitters from nerve terminals .
THEORIES OF PAIN
PERIRHERAL PATTERN THEORY
CENTRAL SUMMATION THEORY SENSORY INTERACTION THEORY
Sinclair & Weddell. 1950. All fiber endings are alike. Pattern of pain is produced by intense stimulation of nonspecific receptors.
Livingstone. 1943. Intense stimulation resulting from nerve & tissue damage activates fibers that project in the spinal cord which in turn projects to brain that underlie pain mechanism.
Noordenbos. 1959. Large fibers inhibits & small fibers excite central transmission neurons.
They postulated that these potentials, which were a reflection of presynaptic inhibition or excitation, modulated the activity of secondary transmitting neurons(T cells) in the dorsal horns, & that this modulation was mediated through an inhibitory interneuron(I cells) placed the T cell in laminaV of the dorsal horn & the still unidentified cells in laminae II & III. The essence of this theory is the large diameter fibers excite the I cells, which in turn causes a presynaptic inhibition of T cells. Conversly the small small afferent fibers inhibits the I cells leaving the T cells in an excitatory state. Impulses from the dorsal horn must also be under the control of a descending system of fibers from brain stem, thalamus .
CARDIOVASCULAR
Stimulation of sympathetic neurons and subsequent tachycardia, increased stroke volume, cardiac work and myocardial oxygen consumption.
Respiratory
Reduced Vital capacity and Forced expiratory
volume.
Decrease of diaphragmatic function Reduced pulmonary compliance, muscle splinting and inability to breathe deeply or cough forcefully leading to hypoxia, hypercarbia, retention of secretions, atelectasis, and pneumonia .
Gastrointestinal and urinary: Ileus, nausea, vomiting, hypo motility of the urethra and bladder.
Neuroendocrine and metabolic: catecholamine and catabolic hormone secretion (cortisol, adrenocorticotrophic hormone(ACTH), antidiuretic hormone, growth hormone, cyclic adenosine monophosphate (CAMP), glucagon, aldosterone, renin, angiotensin 2
References
For all the happiness mankind can gain is not in pleasure but in rest from pain. John Dryden