首页> 外文期刊>British Journal of Pharmacology >Actions of general anaesthetics and arachidonic acid pathway inhibitors on K~+ currents activated by volatile anaesthetics and FMRFamide in molluscan neurones
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Actions of general anaesthetics and arachidonic acid pathway inhibitors on K~+ currents activated by volatile anaesthetics and FMRFamide in molluscan neurones

机译:全身麻醉药和花生四烯酸途径抑制剂对软体动物神经元中挥发性麻醉药和FMRFamide激活的K〜+电流的作用

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摘要

K~+ currents activated by volatile general anaesthetics(I_K(An)) and by the neuropeptide FMRFamide (I_K(FMRFa) were studied under voltage clapme in isolated identified neurones from the pond snail Lymnaea stagnalis. I_K(An) was activated by all the volatile anaesthetics studied. The maximal responses varied from agent To agent, with halothane ≈sevoflurane > isoflurane>enflurane ≈chloroform. I_K(An) was inhibited rather than activated by the n-alcohols from hexanol to dodecanol and by the 6- And 8-carbon cycloalcohols. The n-alcohols exhibited a cutoff effect, with dodecanol being unable to Half-inhibit I-K(An).
机译:研究了挥发性全麻药(I_K(An))和神经肽FMRFamide(I_K(FMRFa)在电压互感器的作用下,从分离出的田螺(Lymnaea stagnalis)分离出的神经元中激活的K〜+电流。氟烷麻醉剂中最大的反应因试剂而异,氟烷→七氟醚>异氟烷>氯氟醚≈氯仿I_K(An)被己醇到十二烷的正醇以及6-和8-被抑制而不是被激活。正醇具有截止作用,十二烷醇不能半抑制IK(An)。

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