Nagamatsu K, Inoue K, Terao T, Toki S
Biochem Pharmacol. 1986 May 15;35(10):1675-8. doi: 10.1016/0006-2952(86)90322-9.
The ability of sulfhydryl compounds to provide protection against the acute toxicity of codeinone, a toxic metabolite of codeine, was investigated in mice. Subcutaneous administration of codeinone produced a slight reduction in hepatic glutathione concentration. Pretreatment of the mice with glutathione or cysteine significantly increased the survival rate for mice given a lethal dose of codeinone (10 mg/kg). The lethality of codeine was lowered by naloxone, whereas that of codeinone was not blocked by naloxone. The strychnine-like convulsant action of codeinone could be prevented by phenobarbital pretreatment. Glutathione pretreatment reduced the amounts of radioactivity in tissues of mice injected with [N-methyl-3-H]codeinone. A possible explanation for these observations is that glutathione reacts in vivo with codeinone and plays a role as a scavenger of this compound. This assumption is supported by the observation that codeinone reacts non-enzymatically with glutathione under physiological conditions.
在小鼠中研究了巯基化合物对可待因的有毒代谢产物可待因酮急性毒性的保护能力。皮下注射可待因酮会使肝脏谷胱甘肽浓度略有降低。用谷胱甘肽或半胱氨酸对小鼠进行预处理,可显著提高给予致死剂量可待因酮(10毫克/千克)的小鼠的存活率。纳洛酮可降低可待因的致死性,但可待因酮的致死性不受纳洛酮的阻断。苯巴比妥预处理可预防可待因酮的士的宁样惊厥作用。谷胱甘肽预处理可减少注射了[甲基-3-H]可待因酮的小鼠组织中的放射性。对这些观察结果的一种可能解释是,谷胱甘肽在体内与可待因酮发生反应,并作为该化合物的清除剂发挥作用。生理条件下可待因酮与谷胱甘肽发生非酶反应这一观察结果支持了这一假设。