Literature DB >> 8601803

Changes in action potential duration alter reliance of excitatory synaptic transmission on multiple types of Ca2+ channels in rat hippocampus.

D B Wheeler1, A Randall, R W Tsien.   

Abstract

It has been established that multiple types of Ca2+ channels participate in triggering neurotransmitter release at central synapses, but there is uncertainty about the nature of their combined actions. We investigated synaptic transmission at CA3-CA1 synapses of rat hippocampal slices and asked whether the dependence on omega-CTx-GVIA-sensitive N-type channels and omega-Aga-IVA-sensitive P/Q-type Ca2+ channels can be altered by physiological mechanisms. The reliance on multiple types of Ca2+ channels was not absolute but depended strongly on the amount of Ca2+ influx through individual channels, which was manipulated by prolonging the presynaptic action potential with the K+ channel blocker 4-aminopyridine (4-AP) and by varying the extracellular Ca2+ concentration ([Ca2+]o). We quantified the influence of spike broadening on Ca2+ influx through various Ca2+ channels by imposing mock action potentials on voltage-clamped cerebellar granule neurons. In field recordings of the EPSP in hippocampal slices, action potential prolongation increased the EPSP slope by 2-fold and decreased its reliance on either N-type or P/Q-type Ca2+ channels. The inhibition of synaptic transmission by N-type channel blockade was virtually eliminated in the presence of 4-AP, but it could be restored by lowering [Ca2+]o. These results rule out a scenario in which a significant fraction of presynaptic terminals rely solely on N-type channels to trigger transmission. The change in sensitivity to the neurotoxins with 4-AP could be explained in terms of a nonlinear relationship between Ca2+ entry and synaptic strength, which rises steeply at low [Ca2+]o, but approaches saturation at high [Ca2+]o. This relationship was evaluated experimentally by varying [CA2+]o in the absence and presence of 4-AP. One consequence of this relationship is that down-modulation of presynaptic Ca2+ channels by various modulators would increase the relative impact of spike broadening greatly.

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Year:  1996        PMID: 8601803      PMCID: PMC6578534     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  67 in total

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Journal:  J Neurosci       Date:  2000-02-01       Impact factor: 6.167

2.  Synchronized paroxysmal activity in the developing thalamocortical network mediated by corticothalamic projections and "silent" synapses.

Authors:  P Golshani; E G Jones
Journal:  J Neurosci       Date:  1999-04-15       Impact factor: 6.167

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4.  Presynaptic Ca2+ channels and neurotransmitter release at the terminal of a mouse cortical neuron.

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Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

5.  Baclofen and adenosine inhibition of synaptic transmission at CA3-CA1 synapses display differential sensitivity to K+ channel blockade.

Authors:  Jane Skov; Mogens Andreasen; John J Hablitz; Steen Nedergaard
Journal:  Cell Mol Neurobiol       Date:  2011-01-28       Impact factor: 5.046

6.  Characterization of release-independent short-term depression in the juvenile rat hippocampus.

Authors:  J Muñoz-Cuevas; H Vara; A Colino
Journal:  J Physiol       Date:  2004-06-04       Impact factor: 5.182

7.  G protein {beta}{gamma} subunits mediate presynaptic inhibition of transmitter release from rat superior cervical ganglion neurones in culture.

Authors:  Gary J Stephens; Sumiko Mochida
Journal:  J Physiol       Date:  2005-01-20       Impact factor: 5.182

Review 8.  Homeostatic regulation of glutamate release in response to depolarization.

Authors:  Krista L Moulder; Julian P Meeks; Steven Mennerick
Journal:  Mol Neurobiol       Date:  2006-04       Impact factor: 5.590

9.  Chronic stress dampens excitatory synaptic gain in the paraventricular nucleus of the hypothalamus.

Authors:  Eric W Salter; Julia K Sunstrum; Sara Matovic; Wataru Inoue
Journal:  J Physiol       Date:  2018-07-22       Impact factor: 5.182

10.  The rate of information transfer of naturalistic stimulation by graded potentials.

Authors:  Mikko Juusola; Gonzalo G de Polavieja
Journal:  J Gen Physiol       Date:  2003-07-14       Impact factor: 4.086

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