Increases in urinary enzyme excretion in rats depleted of glutathione inhibited by scavenger of oxygen free radicals.

M Gemba, T Yamaguchi, K Kambara, A Suzuki, Y Kawai
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引用次数: 8

Abstract

Urinary excretion of enzymes by rats was assessed after glutathione (GSH) was depleted by treatment with a mixture of the GSH depletors D,L-buthionine-S,R-sulfoximine (BSO) and diethylmaleate (DEM). Renal GSH was low 2 h after treatment and later returned to the control level. The urinary excretion of gamma-glutamyltranspeptidase (gamma-GTP) and N-acetyl-beta-D-glucosaminidase (NAG) remained high for at least 3 d after the injection of BSO (100 mg/kg) and DEM (0.5 ml/kg), with no effect on the blood urea nitrogen level. N,N'-Dimethylthiourea (DMTU), a scavenger of oxygen free radicals, inhibited this increase in the urinary excretion of gamma-GTP. DMTU also inhibited the increase in cisplatin-induced NAG excretion caused by the GSH depletors. These results suggested that the urinary excretion of these enzymes is an index of renal tubular injury caused by short-term depletion of renal GSH, and that the generation of free radicals may be involved in renal tubular injury during GSH depletion or caused by cisplatin together with GSH depletors.

氧自由基清除剂抑制谷胱甘肽耗竭大鼠尿酶排泄的增加。
用谷胱甘肽(GSH)消耗物D、l -丁硫氨酸-s、r -亚砜胺(BSO)和马来酸二乙酯(DEM)的混合物处理谷胱甘肽(GSH)后,评估大鼠尿液中酶的排泄。治疗后2小时肾GSH较低,随后恢复到对照水平。注射BSO (100 mg/kg)和DEM (0.5 ml/kg)后,尿中γ -谷氨酰转肽酶(γ - gtp)和n -乙酰- β - d -氨基葡萄糖苷酶(NAG)的排泄量保持高水平至少3 d,对血尿素氮水平无影响。N,N'-二甲基硫脲(DMTU),一种氧自由基清除剂,抑制了尿中γ - gtp排泄的增加。DMTU还抑制GSH消耗物引起的顺铂诱导的NAG排泄增加。这些结果提示尿中这些酶的排泄是肾GSH短期耗竭引起的肾小管损伤的一个指标,自由基的产生可能参与GSH耗竭时或顺铂与GSH耗竭物共同引起的肾小管损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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