Ultrafast and Slow Cholinergic Transmission. Different Involvement of Acetylcholinesterase Molecular Forms

Acetylcholine (ACh), an ubiquitous mediator substance broadly expressed in nature, acts as neurotransmitter in cholinergic synapses, generating specific communications with different time-courses. (1) Ultrafast transmission. Vertebrate neuromuscular junctions (NMJs) and nerve-electroplaque junctions...

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出版年:Molecules
主要な著者: Yves Dunant, Victor Gisiger
フォーマット: 論文
言語:英語
出版事項: MDPI AG 2017-08-01
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オンライン・アクセス:https://www.mdpi.com/1420-3049/22/8/1300
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author Yves Dunant
Victor Gisiger
author_facet Yves Dunant
Victor Gisiger
author_sort Yves Dunant
collection DOAJ
container_title Molecules
description Acetylcholine (ACh), an ubiquitous mediator substance broadly expressed in nature, acts as neurotransmitter in cholinergic synapses, generating specific communications with different time-courses. (1) Ultrafast transmission. Vertebrate neuromuscular junctions (NMJs) and nerve-electroplaque junctions (NEJs) are the fastest cholinergic synapses; able to transmit brief impulses (1–4 ms) at high frequencies. The collagen-tailed A12 acetylcholinesterase is concentrated in the synaptic cleft of NMJs and NEJs, were it curtails the postsynaptic response by ultrafast ACh hydrolysis. Here, additional processes contribute to make transmission so rapid. (2) Rapid transmission. At peripheral and central cholinergic neuro-neuronal synapses, transmission involves an initial, relatively rapid (10–50 ms) nicotinic response, followed by various muscarinic or nicotinic effects. Acetylcholinesterase (AChE) being not concentrated within these synapses, it does not curtail the initial rapid response. In contrast, the late responses are controlled by a globular form of AChE (mainly G4-AChE), which is membrane-bound and/or secreted. (3) Slow ACh signalling. In non-neuronal systems, in muscarinic domains, and in most regions of the central nervous system (CNS), many ACh-releasing structures (cells, axon terminals, varicosities, boutons) do not form true synaptic contacts, most muscarinic and also part of nicotinic receptors are extra-synaptic, often situated relatively far from ACh releasing spots. A12-AChE being virtually absent in CNS, G4-AChE is the most abundant form, whose function appears to modulate the “volume” transmission, keeping ACh concentration within limits in time and space.
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spelling doaj-art-4c88750fa95f4eb4bc48fc6a6ce558d22025-08-19T21:58:10ZengMDPI AGMolecules1420-30492017-08-01228130010.3390/molecules22081300molecules22081300Ultrafast and Slow Cholinergic Transmission. Different Involvement of Acetylcholinesterase Molecular FormsYves Dunant0Victor Gisiger1Département des Neurosciences Fondamentales, Faculté de Médecine, Université de Genève, CH-1211-Genève 4, SwitzerlandDépartement de Pathologie et Biologie Cellulaire, Faculté de Médecine, Université de Montréal, Montréal QC H3C 3J7, CanadaAcetylcholine (ACh), an ubiquitous mediator substance broadly expressed in nature, acts as neurotransmitter in cholinergic synapses, generating specific communications with different time-courses. (1) Ultrafast transmission. Vertebrate neuromuscular junctions (NMJs) and nerve-electroplaque junctions (NEJs) are the fastest cholinergic synapses; able to transmit brief impulses (1–4 ms) at high frequencies. The collagen-tailed A12 acetylcholinesterase is concentrated in the synaptic cleft of NMJs and NEJs, were it curtails the postsynaptic response by ultrafast ACh hydrolysis. Here, additional processes contribute to make transmission so rapid. (2) Rapid transmission. At peripheral and central cholinergic neuro-neuronal synapses, transmission involves an initial, relatively rapid (10–50 ms) nicotinic response, followed by various muscarinic or nicotinic effects. Acetylcholinesterase (AChE) being not concentrated within these synapses, it does not curtail the initial rapid response. In contrast, the late responses are controlled by a globular form of AChE (mainly G4-AChE), which is membrane-bound and/or secreted. (3) Slow ACh signalling. In non-neuronal systems, in muscarinic domains, and in most regions of the central nervous system (CNS), many ACh-releasing structures (cells, axon terminals, varicosities, boutons) do not form true synaptic contacts, most muscarinic and also part of nicotinic receptors are extra-synaptic, often situated relatively far from ACh releasing spots. A12-AChE being virtually absent in CNS, G4-AChE is the most abundant form, whose function appears to modulate the “volume” transmission, keeping ACh concentration within limits in time and space.https://www.mdpi.com/1420-3049/22/8/1300acetylcholineacetylcholinesteraseneuromuscular junctionelectric organ synaptic transmissioncholinergic synapsesnon-neuronal acetylcholine
spellingShingle Yves Dunant
Victor Gisiger
Ultrafast and Slow Cholinergic Transmission. Different Involvement of Acetylcholinesterase Molecular Forms
acetylcholine
acetylcholinesterase
neuromuscular junction
electric organ synaptic transmission
cholinergic synapses
non-neuronal acetylcholine
title Ultrafast and Slow Cholinergic Transmission. Different Involvement of Acetylcholinesterase Molecular Forms
title_full Ultrafast and Slow Cholinergic Transmission. Different Involvement of Acetylcholinesterase Molecular Forms
title_fullStr Ultrafast and Slow Cholinergic Transmission. Different Involvement of Acetylcholinesterase Molecular Forms
title_full_unstemmed Ultrafast and Slow Cholinergic Transmission. Different Involvement of Acetylcholinesterase Molecular Forms
title_short Ultrafast and Slow Cholinergic Transmission. Different Involvement of Acetylcholinesterase Molecular Forms
title_sort ultrafast and slow cholinergic transmission different involvement of acetylcholinesterase molecular forms
topic acetylcholine
acetylcholinesterase
neuromuscular junction
electric organ synaptic transmission
cholinergic synapses
non-neuronal acetylcholine
url https://www.mdpi.com/1420-3049/22/8/1300
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