Serotonin Flashcards

1
Q

Describe where serotonin is mostly found

A
  • 90% of the 5-HT in your body is found in the gut
  • 5-HT is a major neurotransmitter in the enteric nervous system and is released by enterochromaffin cells
  • 5-HT stimulates peristalsis and
    secretion into the intestines
  • 5-HT is massively released in response to chemical, physical, or pathological stimuli and can activate vagal afferents to signal the brain in generation of nausea & act at the area postrema (chemoreceptor trigger zone)
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2
Q

Describe serotonin synthesis and catabolism

A

Dietary L-tryptophan is transported into the brain where it is converted to 5-HT by tryptophan hydroxylase (the rate limiting enzyme).
5-HT is deaminated by monoamine oxidase to 5-hydroxyindoleacetic acid in the cytoplasm of seratonergic neurons
In contrast to the catecholamines, 5-HT breakdown occurs only through MAO.

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3
Q

Describe tryptophan depletion

A
  • Para-chlorophenylalanine (PCPA) is used in animals to rapidly deplete 5-HT
  • PCPA is an irreversible inhibitor of tryptophan hydroxylase
  • 1-2 doses depletes 5-HT by up to 90% for up to 2 weeks
  • Prolonged effect since new protein synthesis is required
  • Reserpine also depletes 5-HT by inhibiting VMAT
  • Tryptophan can be depleted in humans by administering an amino acid mix devoid of
    tryptophan
  • Boost of amino acids triggers protein synthesis in the liver, depleting previous supply of tryptophan
  • Neutral amino acids compete for BBB transporters
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4
Q

Describe 5 HT releasers

A
  • Fenfluramine
  • Prescribed for weight loss in obese patients
  • Some substituted amphetamines * Para-chloroamphetamine
  • Amphetamine analogue used experimentally
  • 3,4-methylenedioxymethamphetamine (MDMA)
  • Psychoactiverecreationaldrug(Ecstasy)
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5
Q

Describe fen-phen

A
  • Dopamine and 5-HT are directly opposed in regulating appetite
  • Dopamine is released in response to food stimuli (smell), stimulates appetite
  • 5-HT generated as a result of eating inhibits dopamine release, decreasing appetite
  • Fenfluramine is a 5-HT releaser
  • Phentermine supresses appetite through effects on catecholamines (psychostimulant
    similar to amphetamine)
  • Fen-Phen came into use in the 1990’s as an off-label prescription for obesity
  • Co-treatment avoided drowsiness and adverse mood effects associated with fenfluramine
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6
Q

Describe the effects of Fen-Phen

A
  • Fen-Phen was never FDA approved for weight
    loss (off-label use)
  • Several studies published in 1996-7 linked long term Fen-Phen use with severe adverse consequences
  • Heart valve abnormalities
  • Primary pulmonary hypertension – increased blood
    pressure between heart and lungs – often fatal
  • Both fenfluramine (Pondimin) and dexfenfluramine (Redux) removed from clinical use in late 1997
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7
Q

Describe 5-HT transporters

A
  • Responsible for inactivation of 5-HT signalling by reuptake
  • Similar to DAT, NET
  • Many drugs have effects at all three (e.g. cocaine and
    amphetamines, antidepressants)
  • SERT also found in lungs, placenta, and platelets * SERT pumps systemic 5-HT into platelets
  • Functions in clotting cascades as a vasoconstrictor
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8
Q

How is SERT a popular drug target?

A
  • TCA antidepressants (non-selective for SERT, NET)
  • Imipramine
  • SSRIantidepressants(selectiveforSERT)
  • Fluoxetine
  • SNRI antidepressants (non-selective for SERT, NET)
  • Venlafaxine
  • SNDRI antidepressants (SERT ~ NET > DAT)
  • Psychoactive drugs (non-selective for SERT, NET, DAT)
  • Cocaine, amphetamines, MDMA
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