Literature DB >> 7617448

Delayed onset and slow time course of the non-M-type muscarinic current in bullfrog sympathetic neurons.

S Minota1.   

Abstract

The onset and time course of the muscarinic currents induced by brief applications of acetylcholine (ACh) were examined in voltage-clamped neurons of bullfrog sympathetic ganglia bathed in a solution containing d-tubocurarine. At a potential of -40 mV, the ACh-induced current (IACh) appeared within 1.2 s and rapidly increased to its peak with a half-activation time of 2.2 s. This initial current was termed the fast IACh and was blocked by 4 mM Ba2+. At a potential more negative than -60 mV, the fast IACh disappeared and the remaining IACh activated with a delay of 3.9 s and slowly increased to its peak with a half-activation time of 8.2 s. This delayed current was termed the slow IACh and is thought to be associated with inhibition of a K+ current, or IM, as well as activation of an inward current through non-M-type muscarinic cation channels. The slow IACh was not inhibited by Ba2+, but its amplitude was reduced with depolarization (the extrapolated reversal potential was +3 mV). In Na(+)-free solution, the amplitude of the slow IACh reduced, but its polarity did not reverse in the voltage region examined (-30 to -100 mV). The slow excitatory postsynaptic current was also recorded, and was shown to have a similar delay in onset and slow time course. The results demonstrate that ACh activates the non-M-type muscarinic current three times more slowly than it inhibits IM.

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Year:  1995        PMID: 7617448     DOI: 10.1007/BF00704163

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  31 in total

1.  Kinetics of G protein-mediated modulation of the potassium M-current in bullfrog sympathetic neurons.

Authors:  H S Lopez
Journal:  Neuron       Date:  1992-04       Impact factor: 17.173

2.  Agonists that suppress M-current elicit phosphoinositide turnover and Ca2+ transients, but these events do not explain M-current suppression.

Authors:  P J Pfaffinger; M D Leibowitz; E M Subers; N M Nathanson; W Almers; B Hille
Journal:  Neuron       Date:  1988-08       Impact factor: 17.173

3.  Nicotinic acetylcholine receptor-ion channels involved in synaptic currents in bullfrog sympathetic ganglion cells and effects of atropine.

Authors:  S Minota; T Eguchi; K Kuba
Journal:  Pflugers Arch       Date:  1989-07       Impact factor: 3.657

4.  Protein kinase C is not necessary for peptide-induced suppression of M current or for desensitization of the peptide receptors.

Authors:  M M Bosma; B Hille
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

5.  Regulation of two ion channels by a common muscarinic receptor-transduction system in a vertebrate neuron.

Authors:  S Tsuji; S Minota; K Kuba
Journal:  Neurosci Lett       Date:  1987-10-16       Impact factor: 3.046

6.  Generation of slow postsynaptic potentials without increases in ionic conductance.

Authors:  H Kobayashi; B Libet
Journal:  Proc Natl Acad Sci U S A       Date:  1968-08       Impact factor: 11.205

7.  Two muscarinic depolarizing mechanisms in mammalian sympathetic neurons.

Authors:  T Hashiguchi; H Kobayashi; T Tosaka; B Libet
Journal:  Brain Res       Date:  1982-06-24       Impact factor: 3.252

8.  M-current suppression by agonist and phorbol ester in bullfrog sympathetic neurons.

Authors:  N V Marrion
Journal:  Pflugers Arch       Date:  1994-02       Impact factor: 3.657

9.  Peptidergic and muscarinic excitation at amphibian sympathetic synapses.

Authors:  S W Kuffler; T J Sejnowski
Journal:  J Physiol       Date:  1983-08       Impact factor: 5.182

10.  On the transduction mechanism for muscarine-induced inhibition of M-current in cultured rat sympathetic neurones.

Authors:  D A Brown; N V Marrion; T G Smart
Journal:  J Physiol       Date:  1989-06       Impact factor: 5.182

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