Suppr超能文献

谷胱甘肽和活性硫酸盐(PAPS)的合成速率以及谷胱甘肽耗竭的大鼠肝细胞对半胱氨酸和对乙酰氨基酚给药的反应。

Synthesis rates of glutathione and activated sulphate (PAPS) and response to cysteine and acetaminophen administration in glutathione-depleted rat hepatocytes.

作者信息

Dalhoff K, Poulsen H E

机构信息

Department of Medicine A-2152 Rigshospitalet, Copenhagen, Denmark.

出版信息

Biochem Pharmacol. 1993 Oct 5;46(7):1295-7. doi: 10.1016/0006-2952(93)90479-g.

Abstract

The effects of cysteine and acetaminophen (AA) on the synthesis rates of glutathione (GSH), adenosine 3'-phosphate 5'-phosphosulphate (PAPS, activated sulphate) and the AA metabolites, AA-GSH and AA-sulphate were studied in rat hepatocytes depleted of GSH by diethyl maleate (DEM). The synthesis rates were determined simultaneously by a previously described radioactive tracer method. Preincubation of the hepatocytes with 0.7 mM DEM for 30 min depleted GSH by 59% (P < 0.05) and PAPS by 28% (P < 0.05). Incubation with a toxic AA concentration resulted in GSH synthesis at a rate of 95 nmol/(10(6) cells.min) which increased to 281 nmol/(10(6) cells.min) (P = 0.05) after addition of cysteine. However, increased GSH synthesis was not followed by increased AA-GSH synthesis [4.7 vs 4.8 nmol/(10(6) cells.hr)]. Also, PAPS synthesis increased after cysteine administration [10.2 to 19.1 nmol/(10(6) cells.min)] (P < 0.05) without any change in AA-sulphate synthesis 18.5 vs 18.3 nmol/(10(6) cells.hr)]. Thus, in contrast to hepatocytes with normal GSH concentration, cysteine stimulated both GSH and PAPS synthesis rates in GSH-depleted rat hepatocytes incubated with a toxic AA concentration without stimulation of AA-GSH or AA-sulphate synthesis rates, indicating that the hepatoprotective effect of cysteine on AA toxicity is primarily due to stimulation of a GSH-mediated reduction of the reactive AA metabolite N-acetyl-p-benzoquinoneimine back to AA.

摘要

研究了半胱氨酸和对乙酰氨基酚(AA)对经马来酸二乙酯(DEM)处理而耗尽谷胱甘肽(GSH)的大鼠肝细胞中谷胱甘肽(GSH)、3'-磷酸腺苷5'-磷酸硫酸酯(PAPS,活性硫酸盐)以及AA代谢产物AA-GSH和AA-硫酸盐合成速率的影响。通过先前描述的放射性示踪法同时测定合成速率。将肝细胞与0.7 mM DEM预孵育30分钟,使GSH减少59%(P < 0.05),PAPS减少28%(P < 0.05)。用有毒浓度的AA孵育导致GSH合成速率为95 nmol/(10⁶个细胞·分钟),添加半胱氨酸后增加至281 nmol/(10⁶个细胞·分钟)(P = 0.05)。然而,GSH合成增加后,AA-GSH合成并未增加[4.7对4.8 nmol/(10⁶个细胞·小时)]。同样,给予半胱氨酸后PAPS合成增加[从10.2至19.1 nmol/(10⁶个细胞·分钟)](P < 0.05),而AA-硫酸盐合成无变化[18.5对18.3 nmol/(10⁶个细胞·小时)]。因此与GSH浓度正常的肝细胞不同,在与有毒浓度的AA一起孵育的GSH耗尽的大鼠肝细胞中,半胱氨酸刺激了GSH和PAPS的合成速率,而未刺激AA-GSH或AA-硫酸盐的合成速率,这表明半胱氨酸对AA毒性的肝保护作用主要是由于刺激了由GSH介导的将活性AA代谢产物N-乙酰-p-苯醌亚胺还原回AA的过程。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验