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局部麻醉药对线粒体电子传递的多个抑制位点。

Multiple sites of inhibition of mitochondrial electron transport by local anesthetics.

作者信息

Chazotte B, Vanderkooi G

出版信息

Biochim Biophys Acta. 1981 Jul;636(2):153-61. doi: 10.1016/0005-2728(81)90088-8.

Abstract

Local anesthetics and alcohols were found to inhibit mitochondrial electron transport at several points along the chain. THe anesthetics employed were the tertiary amines procaine, tetracaine, dibucaine, and chlorpromazine, and the alcohols were n-butamol, n-pentanol, n-hexanol, and benzyl alcohol. Uncoupled sonic submitochondrial particles from beef heart and rat liver were studied. We report the following: (1) All of the anesthetics were found to inhibit each of the segments of the electron transport chain assayed; these included cytochrome c oxidase, durohydroquinone oxidase, succinate oxidase, NADH oxidase, succinate dehydrogenase, succinate-cytochrome c oxidoreductase, and NADH-cytochrome c oxidoreductase. (2) NADH oxidase and NADH-cytochrome c oxidoreductase required the lowest concentration of anesthetic for inhibition, and cytochrome c oxidase required the highest concentrations. (3) We conclude that there are several points along the chain at which inhibition occurs, the most sensitive being in the region of Complex I (NADH dehydrogenase). (4) Beef heart submitochondrial particles are less sensitive to inhibition than are rat liver particles. (5) Low concentrations of several of the anesthetics gave enhancement of electron transport activity, whereas higher concentrations of the same agents caused inhibition. (6) The concentrations of anesthetics (alcohol and tertiary amine) which gave 50% inhibition of NADH oxidase were lower than the reported concentrations required for blockage of frog sciatic nerve.

摘要

研究发现,局部麻醉剂和酒精可在呼吸链的多个位点抑制线粒体电子传递。所使用的麻醉剂为叔胺类的普鲁卡因、丁卡因、布比卡因和氯丙嗪,酒精为正丁醇、正戊醇、正己醇和苯甲醇。对来自牛心和大鼠肝脏的解偶联超声亚线粒体颗粒进行了研究。我们报告如下:(1)所有麻醉剂均能抑制所检测的电子传递链的各个片段;这些片段包括细胞色素c氧化酶、杜罗氢醌氧化酶、琥珀酸氧化酶、NADH氧化酶、琥珀酸脱氢酶、琥珀酸 - 细胞色素c氧化还原酶和NADH - 细胞色素c氧化还原酶。(2)NADH氧化酶和NADH - 细胞色素c氧化还原酶对麻醉剂抑制所需的浓度最低,而细胞色素c氧化酶所需浓度最高。(3)我们得出结论,呼吸链上有几个抑制发生的位点,最敏感的区域在复合体I(NADH脱氢酶)区域。(4)牛心亚线粒体颗粒比大鼠肝脏颗粒对抑制更不敏感。(5)几种麻醉剂的低浓度可增强电子传递活性,而相同药物的高浓度则导致抑制。(6)使NADH氧化酶产生50%抑制的麻醉剂(酒精和叔胺)浓度低于报道的阻断青蛙坐骨神经所需的浓度。

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