Role of glutathione conjugation in protection of weanling rat liver against acetaminophen-induced hepatotoxicity

被引:29
|
作者
Allameh, A [1 ]
Vansoun, EY [1 ]
Zarghi, A [1 ]
机构
[1] SHAHID BEHESHTI MED UNIV,FAC PHARM,TEHRAN,IRAN
关键词
acetaminophen; glutathione conjugation; weanling rat; N-acetylcystein;
D O I
10.1016/S0047-6374(97)01862-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The rate of glutathione (GSH) conjugate formation to acetaminophen (APAP) in livers of weanling and adult rats treated with a single i.p. dose of APAP was compared. HPLC analysis of cytosolic fractions revealed that the rate of conjugation in weanling rat is 24-times greater than that of adults. Increased rate of GSH conjugation was independent of the age-related difference observed in liver GSH content. The normal level of liver GSH in weanling rat was 57% of adult level. APAP treatment depleted GSH more significantly in weanling rats as compared to that in adults. N-acetylcystein (NAC) alone had little influence on liver GSH levels. However it was successful in reducing GSH depletion in tissues of growing rats. A 32% repletion in hepatic GSH level in NAC-treated weanling rats was associated with a further 13-fold increase in the rate of GSH conjugate formation. These data together with histopathological results, clearly showed that the inducible GSH system in weanling rat liver act as a safe guard against APAP toxicity. A surge in the rate of APAP-GSH conjugation in growing liver may function in compensation of other detoxification pathways which are saturated more readily at this age. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:71 / 79
页数:9
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