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氯胺酮、苯环己哌啶和苯巴比妥对大鼠胆固醇代谢的影响。

Influence of ketamine, phenylcyclidine, and phenobarbital on cholesterol metabolism in rats.

作者信息

Kritchevsky D, Tepper S A, Davidson L M, Story J A

出版信息

Proc Soc Exp Biol Med. 1976 Mar;151(3):445-7. doi: 10.3181/00379727-151-39231.

Abstract

The effects of ip injections of phenobarbital (100 mg/kg), phenylcyclidine (Sernylan; [1-(1-phenylcyclohexyl)-piperidine-HBl] (1 mg/kg), and ketamine (Ketaset; [dl)2-O-chlorophenyl)-2-(methylamino)cyclohexanone-HCl] (1 mg/kg) on lipid metabolism in rats were compared. This study was undertaken to determine whether the two sedatives currently used in primates share any of the undesirable effects of phenobarbital on lipid metabolism. All three compounds were administered to male Wistar rats for 6 days. Phenobarbital was hepatomegalic, stimulated 7alpha hydroxylation of cholesterol, and inhibited cholesterol synthesis by rat liver slices from mevalonate, but not acetate. The two other sedatives exhibited effects very similar to those observed in the controls. From our work in rats it is concluded that the use of Sernylan or Ketaset for sedation of nonhuman primates will not significantly affect these parameters of lipid metabolism.

摘要

比较了腹腔注射苯巴比妥(100毫克/千克)、苯环己哌啶(赛尼哌;[1-(1-苯基环己基)-哌啶-HBr])(1毫克/千克)和氯胺酮(凯他敏;[(±)2-邻氯苯基-2-(甲氨基)环己酮-HCl])(1毫克/千克)对大鼠脂质代谢的影响。进行这项研究是为了确定目前在灵长类动物中使用的两种镇静剂是否具有苯巴比妥对脂质代谢的任何不良影响。将所有三种化合物给雄性Wistar大鼠连续给药6天。苯巴比妥导致肝脏肿大,刺激胆固醇的7α-羟化,并抑制大鼠肝切片从甲羟戊酸而非乙酸合成胆固醇。另外两种镇静剂表现出与对照组非常相似的效果。从我们在大鼠身上的研究得出结论,使用赛尼哌或凯他敏对非人类灵长类动物进行镇静不会显著影响这些脂质代谢参数。

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