Biogenic amine receptor: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Robert Badgett
imported>Robert Badgett
(→‎Dopamine receptors: Moved text to new dopamine article)
Line 16: Line 16:


====Dopamine receptors====
====Dopamine receptors====
Dopamine is "one of the catecholamine neurotransmitters in the brain. It is derived from tyrosine and is the precursor to norepinephrine and epinephrine. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement."<ref name="MeSH-Dopamine">{{MeSH|Dopamine}}</ref> Dopamine is also the major factor regulating the secretion of [[prolactin]] from the [[anterior pituitary gland]]; in this case, dopamine is released from specialised neurons of the [[arcuate nucleus]] of the [[hypothalamus]] into the blood vessels of the median eminence, which transport the dopamine to the pituitary gland where it inhibits prolactin secretion from lactotroph cells.
[[Dopamine]] receptors are "cell-surface proteins that bind dopamine with high affinity and trigger intracellular changes influencing the behavior of cells."<ref name="MeSH-DopamineReceptors">{{MeSH|Receptors, Dopamine}}</ref>
 
Dopamine receptors are "cell-surface proteins that bind dopamine with high affinity and trigger intracellular changes influencing the behavior of cells."<ref name="MeSH-DopamineReceptors">{{MeSH|Receptors, Dopamine}}</ref>


=====D<sub>1</sub>-like receptors=====
=====D<sub>1</sub>-like receptors=====

Revision as of 06:36, 9 September 2009

This article is developing and not approved.
 Main Article
 Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
https://en.citizendium.org/wiki/index.php?title=Biogenic_amine_receptor&printable=yes
This editable Main Article is under development and subject to a disclaimer.

Biogenic amine receptors are "cell surface proteins that bind biogenic amines with high affinity and regulate intracellular signals which influence the behavior of cells. Biogenic amine is a chemically imprecise term which, by convention, includes the catecholamines epinephrine, norepinephrine (also known as adrenaline and noradrenaline respectively), and dopamine, the indoleamine serotonin, the imidazolamine histamine, and compounds closely related to each of these."[1]

Biogenic amines are a "group of naturally occurring amines derived by enzymatic decarboxylation of the natural amino acids. Many have powerful physiological effects (e.g., histamine, serotonin, epinephrine, tyramine). Those derived from aromatic amino acids, and also their synthetic analogs (e.g., amphetamine), are of use in pharmacology."[2]

Some biogenic amines, including dopamine, serotonin, and acetylcholine, are neurotransmitters.

Classification

Catecholamine receptors

Catecholamines are epinephrine, norepinephrine, dopamine. They are derived from the non-essential amino acid tyrosine which is found in casein in milk and cheese.

Catecholamine receptors are "cell surface proteins that bind catecholamines with high affinity and trigger intracellular changes which influence the behavior of cells. The catecholamine messengers epinephrine, norepinephrine, and dopamine are synthesized from tyrosine by a common biosynthetic pathway."[3]

Adrenergic receptors

For more information, see: Adrenergic receptor.


Dopamine receptors

Dopamine receptors are "cell-surface proteins that bind dopamine with high affinity and trigger intracellular changes influencing the behavior of cells."[4]

D1-like receptors

These receptors stimulate adenylate cyclase.[5]

D1 receptors
D5 receptors
D2-like receptors

These receptors inhibit adenylate cyclase.[6]

Dopamine D2 receptors

Agonists, such as metoclopramide, are used as antiemetics.

Antagonists, such as risperidone and haloperidol, are used to treat schizophrenia.[7]

Blockade of the D2 receptors, which may be predisposed by genetic polymorphisms of the allele, may cause neuroleptic malignant syndrome.[8]

D3 receptors

Agonists of D3, especially nonergot agonists such as pramipexole and ropinirole, may be used to treat Parkinonism and restless legs syndrome.[9]

D4 receptors

Histamine receptors

Histamine is an "amine derived by enzymatic decarboxylation of histidine. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter."[10]

Histamine receptors are "cell-surface proteins that bind histamine and trigger intracellular changes influencing the behavior of cells. Histamine receptors are widespread in the central nervous system and in peripheral tissues. Three types have been recognized and designated H1, H2, and H3. They differ in pharmacology, distribution, and mode of action."[11]

Histamine H1 receptors

Histamine H1 receptors "operate through the inositol phosphate/diacylglycerol second messenger system. Among the many responses mediated by these receptors are smooth muscle contraction, increased vascular permeability, hormone release, and cerebral glyconeogenesis."[12]

Antagonists, such as chorpheniramine, are used to treat allergic rhinitis.

Histamine H2 receptors

Histamine H2 receptors "act via G-proteins to stimulate adenylate cyclase. Among the many responses mediated by these receptors are gastric acid secretion, smooth muscle relaxation, inotropic and chronotropic effects on heart muscle, and inhibition of lymphocyte function."[13]

Antagonists, such as ranitidine, are used to treat gastrointestinal disorder such as peptic ulcer disease and gastroesophageal reflux disease that are due to hyperacidity.

Histamine H3 receptors

Histamine H3 receptors were "first recognized as inhibitory autoreceptors on histamine-containing nerve terminals and have since been shown to regulate the release of several neurotransmitters in the central and peripheral nervous systems.[14]

Serotonin receptors

Serotonin is a "biochemical messenger and regulator, synthesized from the essential amino acid L-tryptophan. In humans it is found primarily in the central nervous system, gastrointestinal tract, and blood platelets. Serotonin mediates several important physiological functions including neurotransmission, gastrointestinal motility, hemostasis, and cardiovascular integrity."[15]

Serotonin receptors are "cell-surface proteins that bind serotonin and trigger intracellular changes which influence the behavior of cells. Several types of serotonin receptors have been recognized which differ in their pharmacology, molecular biology, and mode of action."[16]

Serotonin 5-HT1 receptors

Serotonin 5-HT1 receptors are in the central nervous system. Excess serotonin availability at the serotonin 1A receptor causes serotonin syndrome.

Agonists of serotonin 5-HT1D, such as sumatriptan, are used to treat migraine headaches.[17]

Serotonin 5-HT2 receptors

Antagonists, such as risperidone, are used to treat schizophrenia. Agonists, such as fluoxetine, are used to treat depression.

Serotonin 5-HT3 receptors

Serotonin 5-HT3 receptors stimulate gastrointestinal motility.

Antagonists, such as ondansetron, are used as an antiemetic for chemotherapy.[18] Antagonists, such as alosetron, are to treat diarrhea-predominant irritable bowel syndrome.

Serotonin 5-HT4 receptors

Serotonin 5-HT4 receptors stimulate gastrointestinal motility.

Agonists, such as tegaserod, are used to treat constipation-predominant irritable bowel syndrome.[19]

Amines in disease

Amine hypothesis and depression

Depletion of the amines serotonin and norepinephrine may contribute to depression.[20]

Dopamine hypothesis and schizophrenia

The dopamine hypothesis proposes that schizophrenia is in part due to excessive dopaminergic activity.[21]

References

  1. ↑ Anonymous (2024), Biogenic amine receptor (English). Medical Subject Headings. U.S. National Library of Medicine.
  2. ↑ Anonymous (2024), Biogenic Amines (English). Medical Subject Headings. U.S. National Library of Medicine.
  3. ↑ Anonymous (2024), Receptors, Catecholamine (English). Medical Subject Headings. U.S. National Library of Medicine.
  4. ↑ Anonymous (2024), Receptors, Dopamine (English). Medical Subject Headings. U.S. National Library of Medicine.
  5. ↑ Anonymous (2024), Receptors, Dopamine D1 (English). Medical Subject Headings. U.S. National Library of Medicine.
  6. ↑ Anonymous (2024), Receptors, Dopamine D2 (English). Medical Subject Headings. U.S. National Library of Medicine.
  7. ↑ Katzung, Bertram G. (2001). Basic & clinical pharmacology. New York: Lange Medical Books/McGraw-Hill, 483. ISBN 0-8385-0598-8. 
  8. ↑ Kishida I, Kawanishi C, Furuno T, Kato D, Ishigami T, Kosaka K (2004). "Association in Japanese patients between neuroleptic malignant syndrome and functional polymorphisms of the dopamine D(2) receptor gene". Mol. Psychiatry 9 (3): 293-8. DOI:10.1038/sj.mp.4001422. PMID 15094790. Research Blogging.
  9. ↑ Baker WL, White CM, Coleman CI (2008). "Effect of nonergot dopamine agonists on symptoms of restless legs syndrome". Ann Fam Med 6 (3): 253–62. DOI:10.1370/afm.845. PMID 18474889. Research Blogging.
  10. ↑ Anonymous. Histamine. National Library of Medicine. Retrieved on 2008-01-16.
  11. ↑ Anonymous. Receptors, Histamine. National Library of Medicine. Retrieved on 2008-01-16.
  12. ↑ Anonymous. Receptors, Histamine H1. National Library of Medicine. Retrieved on 2008-01-16.
  13. ↑ Anonymous. Receptors, Histamine H2. National Library of Medicine. Retrieved on 2008-01-16.
  14. ↑ Anonymous. Receptors, Histamine H3. National Library of Medicine. Retrieved on 2008-01-16.
  15. ↑ Anonymous. Serotonin. National Library of Medicine. Retrieved on 2008-01-16.
  16. ↑ Anonymous. Receptors, Serotonin. National Library of Medicine. Retrieved on 2008-01-16.
  17. ↑ Katzung, Bertram G. (2001). Basic & clinical pharmacology. New York: Lange Medical Books/McGraw-Hill, 280. ISBN 0-8385-0598-8. 
  18. ↑ Katzung, Bertram G. (2001). Basic & clinical pharmacology. New York: Lange Medical Books/McGraw-Hill, 279. ISBN 0-8385-0598-8. 
  19. ↑ Katzung, Bertram G. (2001). Basic & clinical pharmacology. New York: Lange Medical Books/McGraw-Hill, 1069. ISBN 0-8385-0598-8. 
  20. ↑ Katzung, Bertram G. (2001). Basic & clinical pharmacology. New York: Lange Medical Books/McGraw-Hill, 498. ISBN 0-8385-0598-8. 
  21. ↑ Katzung, Bertram G. (2001). Basic & clinical pharmacology. New York: Lange Medical Books/McGraw-Hill, 479. ISBN 0-8385-0598-8. 
Retrieved from "https://citizendium.org/wiki/index.php?title=Biogenic_amine_receptor&oldid=379121"