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Presynaptic ionotropic receptors and the control of transmitter release.
- Source :
-
Annual review of neuroscience [Annu Rev Neurosci] 1999; Vol. 22, pp. 443-85. - Publication Year :
- 1999
-
Abstract
- The quantity of neurotransmitter released into the synaptic cleft, the reliability with which it is released, and the response of the postsynaptic cell to that transmitter all contribute to the strength of a synaptic connection. The presynaptic nerve terminal is a major regulatory site for activity-dependent changes in synaptic function. Ionotropic receptors for the inhibitory amino acid GABA, expressed on the presynaptic terminals of crustacean motor axons and vertebrate sensory neurons, were the first well-defined mechanism for the heterosynaptic transmitter-mediated regulation of transmitter release. Recently, presynaptic ionotropic receptors for a large range of transmitters have been found to be widespread throughout the central and peripheral nervous systems. In this review, we first consider some general theoretical issues regarding whether and how presynaptic ionotropic receptors are important regulators of presynaptic function. We consider the criteria that should be met to identify a presynaptic ionotropic receptor and its regulatory function and review several examples of presynaptic receptors that meet at least some of those criteria. We summarize the classic studies of presynaptic inhibition mediated by GABA-gated Cl channels and then focus on presynaptic nicotinic ACh receptors and presynaptic glutamate receptors. Finally, we briefly discuss evidence for other types of presynaptic ionotropic receptors.
- Subjects :
- Acetylcholine physiology
Animals
Humans
Ion Channel Gating physiology
Ion Channels physiology
Neural Inhibition physiology
Receptors, Cell Surface metabolism
Receptors, GABA-A physiology
Receptors, Glutamate physiology
Neurotransmitter Agents metabolism
Presynaptic Terminals metabolism
Receptors, Cell Surface physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0147-006X
- Volume :
- 22
- Database :
- MEDLINE
- Journal :
- Annual review of neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 10202545
- Full Text :
- https://doi.org/10.1146/annurev.neuro.22.1.443