Kim H L
Vet Hum Toxicol. 1985 Feb;27(1):1-2.
Pretreatment of mice with the microsomal enzyme inducers and inhibitors modified the toxicity of lobeline sulfate. The intraperitoneal LD50 of lobeline sulfate following SKF 525-A (75 mg/kg), phenobarbital (PB), and 3-methylcholanthrene (3-MC) were 18.3, 85.5 and 82.1 mg/kg, respectively, as compared to that of saline treated controls, 55.3 mg/kg. Pretreatment of mice with disulfiram (DSF), diethylmaleate (DEM), or ethoxyquin hydrochloride (EQ-HC1) exhibited a very slight effect on the toxicity of lobeline sulfate. These results suggest that the hepatic microsomal monooxygenase system, but not glutathione (GSH), is involved in the detoxication of lobeline sulfate.
用微粒体酶诱导剂和抑制剂对小鼠进行预处理,改变了硫酸洛贝林的毒性。与用生理盐水处理的对照组(腹腔注射半数致死量为55.3mg/kg)相比,经SKF 525-A(75mg/kg)、苯巴比妥(PB)和3-甲基胆蒽(3-MC)预处理后,硫酸洛贝林的腹腔注射半数致死量分别为18.3mg/kg、85.5mg/kg和82.1mg/kg。用双硫仑(DSF)、马来酸二乙酯(DEM)或盐酸乙氧喹(EQ-HCl)对小鼠进行预处理,对硫酸洛贝林的毒性影响甚微。这些结果表明,参与硫酸洛贝林解毒过程的是肝脏微粒体单加氧酶系统,而非谷胱甘肽(GSH)。