首页> 外文期刊>Japanese Journal of Pharmacology >Involvement of N-Type Voltage-Activated Ca2+ Channels in the Release of Endogenous Noradrenaline from the Isolated Vascularly Perfused Rat Stomach
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Involvement of N-Type Voltage-Activated Ca2+ Channels in the Release of Endogenous Noradrenaline from the Isolated Vascularly Perfused Rat Stomach

机译:N型电压激活的Ca 2+通道参与从孤立的血管灌注大鼠胃中释放内源性去甲肾上腺素的过程

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References(14) Cited-By(7) We characterized the voltage-activated Ca2+ channels involved in noradrenaline (NA) release from gastric sympathetic neurons using isolated, vascularly perfused rat stomach. The evoked NA release by electrical stimulation of periarterial nerves was abolished by calcium removal from the perfusion medium and by cadmium. ω-Conotoxin GVIA (N-type Ca2+-channel blocker) effectively and ω-conotoxin MVIIC (N/P/Q-type blocker) slightly inhibited the evoked NA, while ω-agatoxin IVA (P-type blocker) had no effect. These results suggest that ω-conotoxin GVIA and ω-conotoxin MVIIC-sensitive N-type Ca2+ channels are involved in NA release from the rat gastric sympathetic nerve terminals.
机译:参考文献(14)Cited-By(7)使用分离的血管灌注大鼠胃,表征了从胃交感神经元释放去甲肾上腺素(NA)释放的电压激活的Ca2 +通道。通过从灌注介质和镉中去除钙,消除了通过电刺激动脉周围神经引起的NA释放。 ω-芋螺毒素GVIA(N型Ca2 +通道阻滞剂)有效,而ω-芋螺毒素MVIIC(N / P / Q型阻滞剂)略微抑制诱发的NA,而ω-毒素毒素IVA(P型阻滞剂)无效。这些结果表明ω-芋螺毒素GVIA和ω-芋螺毒素MVIIC敏感的N型Ca2 +通道参与从大鼠胃交感神经末梢释放NA。

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