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淡水鱼肝脏微粒体——II. 鱼麻醉剂硫酸喹哪啶和三卡因对苯并(a)芘代谢的抑制作用

Hepatic microsomes from freshwater fish--II. Reduction of benzo(a)pyrene metabolism by the fish anesthetics quinaldine sulfate and tricaine.

作者信息

Fabacher D L

出版信息

Comp Biochem Physiol C Comp Pharmacol. 1982;73(2):285-8. doi: 10.1016/0306-4492(82)90122-8.

Abstract
  1. A single in vivo exposure of brook trout (Salvelinus fontinalis) to a 30.0 mg/l solution of quinaldine sulfate or a 112.5 mg/l solution of tricaine for 5 min significantly reduced the in vitro hydroxylation of benzo(a)pyrene. 2. Since quinaldine sulfate and tricaine formed type I and II binding spectra, respectively, with brook trout hepatic cytochrome P-450, these chemicals probably reduced benzo(a)pyrene hydroxylase enzyme activity by altering the form(s) of cytochrome P-450 responsible for this activity. 3. Hepatic microsomal cytochrome P-450 from brook trout treated with tricaine for 5 min and then placed into fresh water for 24 hr had returned to control levels. 4. Caution should be exercised in the use of quinaldine sulfate or tricaine to anesthetize fish prior to analysis of hepatic microsomal mixed function oxidases.
摘要
  1. 将溪红点鲑(Salvelinus fontinalis)在体内单次暴露于30.0毫克/升的硫酸喹哪啶溶液或112.5毫克/升的三卡因溶液中5分钟,可显著降低苯并(a)芘的体外羟基化作用。2. 由于硫酸喹哪啶和三卡因分别与溪红点鲑肝细胞色素P-450形成I型和II型结合光谱,这些化学物质可能通过改变负责该活性的细胞色素P-450的形式来降低苯并(a)芘羟化酶的活性。3. 用三卡因处理5分钟后再置于淡水中24小时的溪红点鲑肝微粒体细胞色素P-450已恢复到对照水平。4. 在使用硫酸喹哪啶或三卡因在分析肝微粒体混合功能氧化酶之前麻醉鱼类时应谨慎。

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