Literature DB >> 9597154

Presynaptic receptors.

R J Miller1.   

Abstract

Activation of different types of G-protein-linked and ionotropic presynaptic receptors has been shown to regulate neurotransmitter release throughout the central and peripheral nervous systems. In the case of G-protein-linked receptors, three major mechanisms have been suggested: (a) inhibition of Ca channels in the nerve terminal; (b) the activation of presynaptic K channels, resulting in a reduction in the effectiveness of the action potential; and (c) direct modulation of one or more components of the neurotransmitter vesicle release apparatus. In the case of ionotropic presynaptic receptors, inhibition of release may be achieved through depolarization of the terminal and inactivation of Na and Ca channels. Activation of presynaptic ionotropic receptors that are appreciably Ca permeable can also enhance the release of transmitters as a result of their ability to raise [Ca]i in the terminal directly. Many transmitters employ several of these mechanisms, thus allowing considerable flexibility in the presynaptic regulation of transmitter release.

Mesh:

Substances:

Year:  1998        PMID: 9597154     DOI: 10.1146/annurev.pharmtox.38.1.201

Source DB:  PubMed          Journal:  Annu Rev Pharmacol Toxicol        ISSN: 0362-1642            Impact factor:   13.820


  89 in total

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3.  N-type calcium channels and their regulation by GABAB receptors in axons of neonatal rat optic nerve.

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6.  G-protein alpha subunit isoforms couple differentially to receptors that mediate presynaptic inhibition at rat hippocampal synapses.

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8.  The C terminus of the Ca channel alpha1B subunit mediates selective inhibition by G-protein-coupled receptors.

Authors:  A A Simen; C C Lee; B B Simen; V P Bindokas; R J Miller
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Review 9.  Metabotropic glutamate receptors in vertebrate retina.

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10.  Presynaptic modulation of the retinogeniculate synapse.

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Journal:  J Neurosci       Date:  2003-04-15       Impact factor: 6.167

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