Snawder J E, Benson R W, Leakey J E, Roberts D W
Division of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, AR 72079.
Life Sci. 1993;52(2):183-9. doi: 10.1016/0024-3205(93)90138-s.
Propylene glycol (PG) decreases the hepatotoxicity of acetaminophen (APAP). To elucidate the mechanism for this response, we measured the effect of PG on the in vitro metabolism of APAP by subcellular liver fractions from 6-10 week-old male B6C3F1 mice. The fractions were assayed for their ability to bioactivate APAP to N-acetyl-p-benzoquinone imine, which was trapped as APAP-glutathione conjugates or APAP-protein adducts, and for dimethyl-nitrosamine-N-demethylase (DMN), 4-nitrophenol hydroxylase (4-NPOH), and phenacetin-O-deethylase (PAD) activities. Activity in the crude mitochondrial-rich (10,000 x g pellet) fraction was low and PG had no effect. PG inhibited DMN and 4-NPOH, indicators of IIE1-dependent activity, and the formation of APAP-glutathione conjugates and APAP-protein adducts in both heavy (15,000 x g pellet) and light (100,000 x g pellet) microsomes. PAD, a measure of IA2-dependent activity, was not inhibited. These data demonstrate that PG selectively inhibits IIE1 activity, including the bioactivation of APAP, and implicates this as the mechanism for PG-mediated protection of APAP hepatotoxicity in mice.
丙二醇(PG)可降低对乙酰氨基酚(APAP)的肝毒性。为阐明这种反应的机制,我们测定了PG对6至10周龄雄性B6C3F1小鼠肝脏亚细胞组分中APAP体外代谢的影响。检测这些组分将APAP生物激活为N - 乙酰 - 对苯醌亚胺的能力,该物质会以APAP - 谷胱甘肽缀合物或APAP - 蛋白质加合物的形式被捕获,同时检测二甲基亚硝胺 - N - 脱甲基酶(DMN)、4 - 硝基苯酚羟化酶(4 - NPOH)和非那西丁 - O - 脱乙基酶(PAD)的活性。富含粗线粒体(10,000×g沉淀)组分中的活性较低,PG对其无影响。PG抑制了DMN和4 - NPOH(IIE1依赖性活性的指标)以及重微粒体(15,000×g沉淀)和轻微粒体(100,000×g沉淀)中APAP - 谷胱甘肽缀合物和APAP - 蛋白质加合物的形成。作为IA2依赖性活性指标的PAD未被抑制。这些数据表明,PG选择性抑制IIE1活性,包括APAP的生物激活,并表明这是PG介导的对小鼠APAP肝毒性保护作用的机制。