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AT-125(阿西维辛)抑制γ-谷氨酰转肽酶对大鼠脑和血浆中谷胱甘肽及半胱氨酸水平的影响。

Effect of inhibition of gamma-glutamyltranspeptidase by AT-125 (acivicin) on glutathione and cysteine levels in rat brain and plasma.

作者信息

Hill K E, Von Hoff D D, Burk R F

出版信息

Invest New Drugs. 1985;3(1):31-4. doi: 10.1007/BF00176821.

Abstract

AT-125 (Acivicin) is an inhibitor of gamma-glutamyltranspeptidase (gamma-GTP) which initiates glutathione catabolism to cysteine. We measured plasma and brain glutathione and cysteine in rats treated with AT-125. Six h after AT-125 treatment, plasma glutathione had increased 6-fold and plasma cysteine had fallen significantly. Brain cysteine fell after 24 h of AT-125 treatment, and brain glutathione had also decreased 18%. AT-125 pretreatment inhibited brain uptake of 35S when it was given as 35S-GSH but had no effect when it was given as 35S-cysteine. These results suggest that plasma glutathione is catabolized by gamma-GTP, and cysteine derived from it is taken up by the brain. N-acetylcysteine was administered to AT-125 treated rats in an attempt to supply cysteine to the brain in the face of gamma-GTP inhibition. N-acetylcysteine supported brain glutathione levels, suggesting that it can serve as a source of cysteine under these conditions.

摘要

AT - 125(阿西维辛)是γ-谷氨酰转肽酶(γ-GTP)的抑制剂,γ-GTP启动谷胱甘肽分解代谢生成半胱氨酸。我们测定了用AT - 125处理的大鼠血浆和脑内的谷胱甘肽及半胱氨酸水平。AT - 125处理6小时后,血浆谷胱甘肽增加了6倍,血浆半胱氨酸显著下降。AT - 125处理24小时后,脑内半胱氨酸下降,脑内谷胱甘肽也减少了18%。当以35S - 谷胱甘肽形式给予时,AT - 125预处理抑制了脑对35S的摄取,但以35S - 半胱氨酸形式给予时则无影响。这些结果表明,血浆谷胱甘肽被γ-GTP分解代谢,由此产生的半胱氨酸被脑摄取。给用AT - 125处理的大鼠施用N - 乙酰半胱氨酸,试图在γ-GTP受抑制的情况下为脑提供半胱氨酸。N - 乙酰半胱氨酸维持了脑内谷胱甘肽水平,表明在这些条件下它可作为半胱氨酸的来源。

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