Thorgeirsson S S, Sasame H A, Mitchell J R, Jollow D J, Potter W Z
Pharmacology. 1976;14(3):205-17. doi: 10.1159/000136597.
The effects of hepatotoxic doses of acetaminophen and furosemide on the function and composition of hepatic endoplasmic reticulum were compared from 3 to 24 h after administration. Acetaminophen caused a significant decrease in microsomal protein concentration as early as 3 h after its administration, but furosemide did not affect the microsomal protein concentration until 24 h after the dose. Both acetaminophen and furosemide decreased the concentrations of cytochrome P-450 and cytochrome b5 in microsomes, and the activity of microsomal ethylmorphine N-demethylase and aniline hydroxylase. Glucose-6-phosphatase and UDP-glucuronyl transferase were not significantly affected by acetaminophen or furosemide administration, and neither diene conjugation nor hepatic triglycerides were increased. Incorporation of 3H-L-leucine into liver proteins was decreased by 50% after the administration of either acetaminophen or furosemide.
比较了给予肝毒性剂量的对乙酰氨基酚和呋塞米后3至24小时内,它们对肝内质网功能和组成的影响。给予对乙酰氨基酚后3小时,微粒体蛋白浓度即显著下降,但给予呋塞米后直到24小时,微粒体蛋白浓度才受到影响。对乙酰氨基酚和呋塞米均降低了微粒体中细胞色素P - 450和细胞色素b5的浓度,以及微粒体乙基吗啡N - 脱甲基酶和苯胺羟化酶的活性。给予对乙酰氨基酚或呋塞米后,葡萄糖-6-磷酸酶和UDP - 葡萄糖醛酸转移酶未受到显著影响,二烯共轭和肝甘油三酯也未增加。给予对乙酰氨基酚或呋塞米后,3H - L - 亮氨酸掺入肝蛋白的量减少了50%。