氯喹和奎宁的体外药理学研究。

Medical biology Pub Date : 1986-01-01
T Y Lot
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引用次数: 0

摘要

采用离体鸡第二扩张肌,在体外比较了胍乙啶、氯喹和奎宁对去甲肾上腺素能神经的影响。研究了氯喹对各组织去甲肾上腺素能神经末梢摄取-甲基-去甲肾上腺素的影响。胍乙啶和阿奎宁对去甲肾上腺素能神经的抑制作用似乎是神经元内介导的。氯喹的抑制作用是可逆的,不受右安非他明的影响。氯喹通过阻断扩张肌的神经元再摄取而引起扩张肌对去甲肾上腺素的超敏反应,因为去神经支配引起的超敏反应没有被氯喹进一步增强。发现氯喹抑制α -甲基去甲肾上腺素的摄取(Uptake1)证实了这一点。Quinacrine对去甲肾上腺素不敏感,这可能是由于它对扩张肌的直接抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The in vitro pharmacology of chloroquine and quinacrine.

The effects of guanethidine, chloroquine and quinacrine on noradrenergic nerves have been compared in vitro using the isolated expansor secundariorum muscle of chicks. The effect of chloroquine on alpha-methyl-noradrenaline uptake by noradrenergic nerve terminals in various tissues were studied. The inhibitory action of guanethidine and quinacrine on noradrenergic nerves appeared to be mediated intraneuronally. The inhibitory action of chloroquine was readily reversible and unaffected by dexamphetamine. Chloroquine caused supersensitivity of the expansor muscle to noradrenaline by blocking its neuronal reuptake since the supersensitivity caused by denervation was not further increased by chloroquine. This was confirmed by the finding that chloroquine inhibited alpha-methylnoradrenaline uptake (Uptake1). Quinacrine did not cause supersensitivity to noradrenaline, possibly due to its direct depressant action on the expansor secundariorum muscle.

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