Dalhoff K, Poulsen H E
Department of Medicine A-2152 Rigshospitalet, Copenhagen, Denmark.
Biochem Pharmacol. 1993 Oct 5;46(7):1295-7. doi: 10.1016/0006-2952(93)90479-g.
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.
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。