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.

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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。
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