Harris S R, Hamrick M E
Department of Pharmacal Sciences, School of Pharmacy, Auburn University, Al 36849-5503.
Res Commun Chem Pathol Pharmacol. 1993 Jan;79(1):23-44.
A 250 mg/kg subcutaneous injection of acetaminophen (APAP) given to fasted mice was hepatotoxic as indicated by elevated serum alanine aminotransferase activity and electron microscopic studies. When extramitochondrial Ca2+ levels were 200 nM or greater, the APAP caused loss of mitochondrial Ca2+ homeostasis in a two step process that represents a sequence of events. The first step occurs 0 to 3 hours after APAP administration and the second step occurs 6 to 12 hours after APAP administration. Loss of mitochondrial Ca2+ homeostasis 6 to 12 hours after APAP correlates chronologically with nuclear damage as indicated by loss of nuclear Ca2+ sequestration between 6 and 12 hours after APAP administration. Pretreatment of mice with the phospholipase A2 (PLA2) inhibitors chlorpromazine or diltiazem one hour prior to APAP administration inhibits loss of mitochondrial Ca2+ homeostasis, prevents nuclear damage, and inhibits APAP hepatotoxicity as indicated by serum alanine aminotransferase activity and electron microscopic studies. This protective effect of chlorpromazine and diltiazem does not interfer with initial actions of APAP that influence mitochondrial function, but interfers with the sequence of events initiated by APAP that leads to loss of mitochondrial Ca2+ homeostasis and hepatotoxicity.
对禁食小鼠皮下注射250 mg/kg对乙酰氨基酚(APAP)会产生肝毒性,血清丙氨酸转氨酶活性升高及电子显微镜研究均表明了这一点。当线粒体外Ca2+水平达到200 nM或更高时,APAP会通过一个两步过程导致线粒体Ca2+稳态失衡,这代表了一系列事件。第一步发生在APAP给药后0至3小时,第二步发生在APAP给药后6至12小时。APAP给药后6至12小时线粒体Ca2+稳态失衡与核损伤在时间上相关,这表现为APAP给药后6至12小时核Ca2+螯合作用丧失。在APAP给药前一小时用磷脂酶A2(PLA2)抑制剂氯丙嗪或地尔硫䓬预处理小鼠,可抑制线粒体Ca2+稳态失衡,防止核损伤,并如血清丙氨酸转氨酶活性和电子显微镜研究所示,抑制APAP肝毒性。氯丙嗪和地尔硫䓬的这种保护作用并不干扰影响线粒体功能的APAP的初始作用,而是干扰由APAP引发的导致线粒体Ca2+稳态失衡和肝毒性的一系列事件。