Medical Pharmacology Chapter 22: Serotonin Pharmacology
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Serotonin is a widely distributed indoleethylamine formed from L-tryptophan:
Serotonin synthesis may be inhibited by p-chlorophenylalanine (PCPA, fenclonine)
Following synthesis, Serotonin may be:
Stored or
Rapidly inactivated by an oxidative step catalyzed by the enzyme, monoamine oxidase or MAO.
Furthermore, in the pineal gland, serotonin serves as a precursor for melatonin which is controlled in part by melanocyte-stimulating hormone.
Most serotonin (> 90%) is stored in enterochromaffin cells , localized in the GI tract.
Blood: platelets concentrate serotonin also and use a active carrier-mediated transport system which is similar to that found in nerve endings.
CNS locations at which serotonin is found include:
Raphe nuclei (brain stem)
In serotonergic neurons, neuronal cell bodies:
Synthesize
Store and
Release
CNS serotonin involvement: include influences on:
Mood
Sleep
Appetite
Temperature regulation
Pain perception
Blood-pressure regulation
Vomiting
Serotonin is degraded by the enzyme, monoamine oxidase, forming: 5-hydroxyindoleacetaldehyde.
5-hydroxyindoleacetaldehyde is then further oxidized in a reaction catalyzed by the enzyme aldehyde dehydrogenase.
The amount of 5-hydroxyindoleacetic acid (5-HIAA) excreted is a measure of serotonin synthesis.
Excessive serotonin synthesis may be helpful as a diagnostic test for certain tumors (e.g. carcinoid).
Serotonin Synthesis and Degradation: Summary
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Burkhalter, A, Julius, D.J. and Katzung, B. Histamine, Serotonin and the Ergot Alkaloids (Section IV. Drugs with Important Actions on Smooth Muscle), in Basic and Clinical Pharmacology, (Katzung, B. G., ed) Appleton-Lange, 1998, pp 261-286.