Moldéus P, Dock L, Cha Y N, Berggren M, Jernström B
Biochem Pharmacol. 1982 May 15;31(10):1907-10. doi: 10.1016/0006-2952(82)90496-8.
Using harmol and paracetamol as the substrates, the elevation of conjugation reactions by BHA feeding and their significance towards the protective effects of this antioxidant has been studied with hepatocytes obtained from mice. With both substrates, an almost five fold elevation of the glucuronidation was observed. However, there was no change in the rate of sulfate conjugation. The rate of glutathione conjugate formation with paracetamol was also not enhanced, even though both the GSH level and glutathione S-transferase activities were increased. Finally, BHA administration afforded no protective effect against the hepatotoxic effects of paracetamol, even when the production of reactive paracetamol metabolites was increased by 3-methylcholanthrene pretreatment.
以去甲骆驼蓬碱和对乙酰氨基酚作为底物,利用从小鼠获取的肝细胞,研究了喂食丁基羟基茴香醚(BHA)后结合反应的增强情况及其对这种抗氧化剂保护作用的意义。对于这两种底物,均观察到葡萄糖醛酸化反应几乎提高了五倍。然而,硫酸结合反应速率没有变化。尽管谷胱甘肽(GSH)水平和谷胱甘肽S-转移酶活性均有所增加,但对乙酰氨基酚的谷胱甘肽结合物形成速率也未提高。最后,即使通过3-甲基胆蒽预处理增加了对乙酰氨基酚活性代谢物的生成,给予BHA对乙酰氨基酚的肝毒性作用也没有保护效果。