Toskulkao C, Lohakachonpan P, Glinsukon T
Department of Physiology, Faculty of Science, Mahidol University, Bangkok, Thialand.
Toxicol Lett. 1991 Jan;55(1):1-9. doi: 10.1016/0378-4274(91)90021-w.
Effect of ethanol pretreatment on acute hepatotoxicity and hepatic fat accumulation induced by aflatoxin B1 (AFB1) was followed up to 120 h in male Wistar rats. Pretreatment with 4 oral doses of ethanol (4.0 g/kg body wt. each) at 48, 45, 24 and 21 h prior to AFB1 (2.0 mg/kg body wt.) single intraperitoneal administration caused a significant increase in the activity of plasma glutamic oxaloacetic transaminase (PGOT, 2.4-fold), plasma glutamic pyruvic transaminase (PGPT, 2.8-fold), liver triglycerides (2.3-fold) and the severity of liver necrosis at 72 h after AFB1 administration. The effect of ethanol pretreatment on an increase in the accumulation of liver cholesterol and cholesterol esters induced by AFB1 is additive in nature. In a time-course study, it was shown that liver necrosis and triglyceride, cholesterol and cholesterol ester accumulation occurred simultaneously in both groups of rats treated with AFB1 and ethanol-AFB1. These results suggest that fat accumulation per se is not a primary cause of liver necrosis induced by AFB1 and ethanol-AFB1.
在雄性Wistar大鼠中,对黄曲霉毒素B1(AFB1)诱导的急性肝毒性和肝脂肪积累,研究乙醇预处理的影响,观察期长达120小时。在单次腹腔注射AFB1(2.0毫克/千克体重)前48、45、24和21小时,用4次口服剂量的乙醇(每次4.0克/千克体重)进行预处理,导致血浆谷草转氨酶(PGOT,2.4倍)、血浆谷丙转氨酶(PGPT,2.8倍)、肝脏甘油三酯(2.3倍)的活性显著增加,以及在AFB1给药后72小时肝脏坏死的严重程度增加。乙醇预处理对AFB1诱导的肝脏胆固醇和胆固醇酯积累增加的影响本质上是相加的。在一项时间进程研究中,结果表明,在用AFB1和乙醇-AFB1处理的两组大鼠中,肝脏坏死以及甘油三酯、胆固醇和胆固醇酯积累同时发生。这些结果表明,脂肪积累本身不是AFB1和乙醇-AFB1诱导肝脏坏死的主要原因。