Monoamine receptor

From Wikipedia, the free encyclopedia
The serotonin 5-HT1B receptor as an example of a monoamine receptor.[1] Its crystallographic structure in ribbon representation.

A monoamine receptor is a receptor for the monoamine neurotransmitters and/or trace amines, endogenous small-molecule signaling molecules with a monoamine structure. The monoamine receptors are almost all G protein-coupled receptors, with the serotonin 5-HT3 receptor being a notable exception as a ligand-gated ion channel.[1] Monoamine receptors are the biological targets of many drugs; such drugs may be referred to as "monoaminergic".

List of receptors[]

Monoamine receptors include the following classes:

  • Adrenergic receptors – bound by epinephrine (adrenaline) and norepinephrine (noradrenaline)
  • Dopamine receptors – bound by dopamine
  • Histamine receptors – bound by histamine
  • Melatonin receptors – bound by melatonin
  • Serotonin receptors – bound by serotonin (5-HT)
  • Trace amine-associated receptors – bound by trace amines, thyronamines, monoamine neurotransmitters (TAAR1 only), and trimethylamine (TAAR5 only)

References[]

  1. ^ a b Martin, Andres; Scahill, Lawrence; Kratochvil, Christopher (14 December 2010). Pediatric Psychopharmacology. Oxford University Press. p. 31. ISBN 9780199842667. Retrieved 27 January 2017. The 5-HT3 receptor is the only monoamine receptor coupled to an ion channel, probably a Ca2+ channel.



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