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  4. Inhibition of the sodium channel by SK&F 96365, an inhibitor of the receptor-operated calcium channel, in mouse diaphragm
 
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Inhibition of the sodium channel by SK&F 96365, an inhibitor of the receptor-operated calcium channel, in mouse diaphragm

Journal
Journal of Biomedical Science
Journal Volume
1
Journal Issue
3
Pages
172-178
Date Issued
1994
Author(s)
Hong S.J.
WAN-WAN LIN  
Chang C.C.
DOI
10.1007/BF02253347
URI
2-s2.0-0007592040
https://scholars.lib.ntu.edu.tw/handle/123456789/550555
Abstract
The effects of SK&F 96365, a blocker of the receptor-operated Ca(2+) channel, on contractilities and the Na(+) channel of mouse diaphragm were studied. SK&F 96365 (10-50 &mgr;M) reversibly inhibited twitches, tetanic contractions and muscle and nerve action potentials. The IC(50) was 17-24 &mgr;M. The inward Na(+) current was suppressed and its recovery from inactivations delayed. Crotamine, a peptide toxin that binds to neurotoxin receptor site 3 of the muscle Na(+) channel, enhanced the inhibitory effects of SK&F 96365 and reduced the IC(50) to about 4 &mgr;M. Veratridine had similar effects, although it was less effective than crotamine. On the other hand, the crotamine-induced membrane depolarizations and spontaneous discharges of muscle action potentials were inhibited by SK&F 96365 noncompetitively. The inhibitory effects of tetrodotoxin and tetracaine were additive with those of SK&F 96365 but were enhanced slightly by crotamine. The results suggested that SK&F 96365 acts on a distinct site and blocks the Na(+) channel fo excitable membranes at a concentration range that inhibits the receptor-operated calcium channel. Copyright 1994 S. Karger AG, Basel
SDGs

[SDGs]SDG6

Type
journal article

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