Modulation of M-channel conductance by adenosine 5
triphosphate in bullfrog sympathetic B-neurones
Authors: Chen H.; Kurennyi D.E.; Smith P.A.
Source: Journal of Autonomic Pharmacology, Volume 21, Number 1, February 2001 , pp. 57-62(6)
Publisher: Wiley-Blackwell
Abstract:
1 Adenosine 5
triphosphate (ATP) (0.5500
M) or muscarine (0.11.0
M) suppressed M-current/conductance (IM/gM) in B-cells of bullfrog sympathetic ganglion. Both agonists suppressed steady-state M-conductance (gM) at 30 mV and there was either no change or a slight increase in the time constants for gM activation (
a at 30 mV) and deactivation (
d at 50 mV).
2 It has previously been shown that experimental elevation of intracellular Ca2+ concentration ([Ca2+]i) suppresses gM and this is associated with decreases in both
a and
d. As these changes in kinetics differ from those we observe with agonist application, our results cast doubt on the hypothesis that elevation of [Ca2+]i is involved in the transduction mechanism for ATP- or muscarine-induced gM suppression.
Keywords: G-protein; potassium channel; activation kinetics; acetylcholine; purinergic receptor; luteinizing hormone releasing hormone
Language: English
Document Type: Research article
Publication date: 2001-02-01
- In this: publication
- By this: publisher
- In this Subject: Pharmacology
- By this author: Chen H. ; Kurennyi D.E. ; Smith P.A.

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