Document Detail


Purinergic cotransmission.
MedLine Citation:
PMID:  18723580     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Adenosine 5'-triphosphate (ATP) is a cotransmitter with classical transmitters in most nerves in the peripheral and central nervous systems, although the proportions vary between tissues and species and in different developmental and pathophysiological circumstances. There was early evidence that ATP was released together with acetylcholine (ACh) from motor nerves supplying skeletal muscle, although it was considered at the time as a molecule involved in the vesicular uptake and storage of ACh. Later it was shown that in the developing neuromuscular junction, released ATP acted on P2X receptor ion channels as a genuine cotransmitter with ACh. Adenosine triphosphate was shown to be released from sympathetic nerves supplying the guinea-pig taenia coli in 1971. Soon after, the possibility was raised that ATP was coreleased with noradrenaline from sympathetic nerves to guinea-pig seminal vesicle, cat nictitating membrane and guinea-pig vas deferens. Sympathetic purinergic cotransmission has also been demonstrated in many blood vessels. Parasympathetic nerves supplying the urinary bladder use ACh and ATP as cotransmitters; ATP acts through P2X ionotropic receptors, whereas the slower component of the response is mediated by the metabotropic muscarinic receptor. Adenosine triphosphate and glutamate appear to be cotransmitters in primary afferent sensory neurons. Adenosine triphosphate, calcitonin gene-related peptide and substance P coexist in some sensory-motor nerves. A subpopulation of intramural enteric nerves provides non-adrenergic, non-cholinergic inhibitory innervation of gut smooth muscle. Three cotransmitters are involved, namely ATP, nitric oxide and vasoactive intestinal polypeptide. In recent years, studies have shown that ATP is released with ACh, noradrenaline, glutamate, gamma-aminobutyric acid, 5-hyroxytryptamine and dopamine in different subpopulations of neurons in the central nervous system.
Authors:
Geoffrey Burnstock
Publication Detail:
Type:  Journal Article     Date:  2008-08-22
Journal Detail:
Title:  Experimental physiology     Volume:  94     ISSN:  1469-445X     ISO Abbreviation:  Exp. Physiol.     Publication Date:  2009 Jan 
Date Detail:
Created Date:  2009-01-06     Completed Date:  2009-04-03     Revised Date:  2010-01-14    
Medline Journal Info:
Nlm Unique ID:  9002940     Medline TA:  Exp Physiol     Country:  England    
Other Details:
Languages:  eng     Pagination:  20-4     Citation Subset:  IM    
Affiliation:
Autonomic Neuroscience Centre, Royal Free and University College Medical School, Rowland Hill Street, London NW3 2PF, UK. g.burnstock@ucl.ac.uk
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MeSH Terms
Descriptor/Qualifier:
Acetylcholine / metabolism
Adenosine Triphosphate / metabolism*
Animals
Central Nervous System / physiology*
Glutamic Acid / metabolism
Humans
Neurotransmitter Agents / metabolism
Nitric Oxide / metabolism
Norepinephrine / metabolism
Peripheral Nervous System / physiology*
Purines / metabolism*
Receptors, Purinergic P2 / physiology
Synaptic Transmission / physiology*
Vasoactive Intestinal Peptide / metabolism
Chemical
Reg. No./Substance:
0/Neurotransmitter Agents; 0/Purines; 0/Receptors, Purinergic P2; 0/purinergic P2X receptor; 10102-43-9/Nitric Oxide; 37221-79-7/Vasoactive Intestinal Peptide; 51-41-2/Norepinephrine; 51-84-3/Acetylcholine; 56-65-5/Adenosine Triphosphate; 56-86-0/Glutamic Acid

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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