Kisara S, Furusawa S, Takayanagi Y, Sasaki K
Department of Pharmacology and Toxicology, Tohoku College of Pharmacy, Sendai, Japan.
Res Commun Mol Pathol Pharmacol. 1995 Sep;89(3):401-10.
The role of the glutathione (GSH) system in vivo or in drug resistance has received much attention, since GSH is a major component of the cellular detoxification system. We Studied the effect of GSH depletion by buthionine sulfoximine (BSO), a potent inhibitor of gamma-glutamylcysteine synthetase, on doxorubicin (DOX) toxicity in mice. The administration of BSO (30 mM in drinking water for 5 days) significantly decreased the tissue GSH. The GSH depletion in various tissues by BSO was associated with a decrease in the detoxification of DOX in mice. A single dose of 20 mg/kg of DOX significantly reduced body weight and rectal temperature in mice 3 days after injection. The combination with BSO and cepharanthine (biscoclaurine alkaloid), a P-glycoprotein (P-gp) inhibitor, significantly potentiated decrease in body and hypothermia induced by DOX. The study demonstrates that BSO markedly increases the toxicological effect of DOX with the alterations in GSH of tissues and Suggests that the intracellular accumulation of DOX is not a factor.
由于谷胱甘肽(GSH)是细胞解毒系统的主要成分,其在体内或耐药性中的作用备受关注。我们研究了丁硫氨酸亚砜胺(BSO,γ-谷氨酰半胱氨酸合成酶的强效抑制剂)消耗GSH对小鼠阿霉素(DOX)毒性的影响。给予BSO(饮用水中30 mM,持续5天)可显著降低组织GSH水平。BSO导致的各组织GSH消耗与小鼠体内DOX解毒作用降低相关。注射20 mg/kg单剂量DOX后3天,小鼠体重和直肠温度显著降低。将BSO与粉防己碱(双苄基异喹啉生物碱,一种P-糖蛋白(P-gp)抑制剂)联合使用,可显著增强DOX诱导的体重下降和体温降低。该研究表明,BSO通过改变组织GSH水平显著增强了DOX的毒理学效应,并表明DOX的细胞内蓄积并非一个因素。