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急性黄曲霉毒素B1诱导的肝毒性改变大鼠基因表达并扰乱脂质和脂蛋白代谢。

Acute aflatoxin B1 - Induced hepatotoxicity alters gene expression and disrupts lipid and lipoprotein metabolism in rats.

作者信息

Rotimi Oluwakemi Anuoluwapo, Rotimi Solomon Oladapo, Duru Chibueze Uchechukwu, Ebebeinwe Ogheneworo Joel, Abiodun Anthonia Obhio, Oyeniyi Boluwaji Oluwamayowa, Faduyile Francis Adedayo

机构信息

Biochemistry Unit and Molecular Biology Research Laboratory, Department of Biological Sciences, Covenant University, Ota, Ogun State, Nigeria.

Department of Pathology and Forensic Medicine, Lagos State University Teaching Hospital, Ikeja, Lagos, Nigeria.

出版信息

Toxicol Rep. 2017 Jul 24;4:408-414. doi: 10.1016/j.toxrep.2017.07.006. eCollection 2017.

Abstract

In this study, alterations in lipid metabolism associated with acute aflatoxin B1 (AFB1) induced hepatotoxicity and gene expression changes underlying these effects were investigated. Rats were orally administered three doses (0.25 mg/kg, 0.5 mg/kg and 1.0 mg/kg) of AFB1 for seven days; after which blood was collected and liver excised. Lipid profiles of plasma and liver were determined spectrophotometrically while the expression of genes associated with lipid and lipoprotein metabolism was assayed by reverse transcriptase polymerase chain reaction. Acute exposure to AFB1 increased the levels of plasma and liver cholesterol, triglycerides and phospholipids. AFB1 at 0.5 mg/kg and 1.0 mg/kg resulted in a dose-dependent (1.2 and 1.5 fold, respectively) downregulation of hepatic with a concomitant 1.2 and 1.5 fold increase in the level of plasma FFA, respectively. A similar observation of 1.2 and 1.3 fold increase was also observed in plasma triglyceride concentration, at both respective doses. AFB1 also decreased the relative expression of and whereas, it upregulated in a dose dependent manner. AFB1-induced dysregulation of the expression of lipid and lipoprotein metabolizing genes may be one mechanism linking AFB1 to altered lipid metabolism and ultimately risk for coronary heart disease.

摘要

在本研究中,研究了与急性黄曲霉毒素B1(AFB1)诱导的肝毒性相关的脂质代谢变化以及这些效应背后的基因表达变化。给大鼠口服三种剂量(0.25mg/kg、0.5mg/kg和1.0mg/kg)的AFB1,持续7天;之后采集血液并切除肝脏。用分光光度法测定血浆和肝脏的脂质谱,同时通过逆转录聚合酶链反应测定与脂质和脂蛋白代谢相关的基因表达。急性暴露于AFB1会增加血浆和肝脏中胆固醇、甘油三酯和磷脂的水平。0.5mg/kg和1.0mg/kg的AFB1分别导致肝脏中剂量依赖性下调(分别为1.2倍和1.5倍),同时血浆游离脂肪酸水平分别增加1.2倍和1.5倍。在各自的剂量下,血浆甘油三酯浓度也观察到类似的1.2倍和1.3倍增加。AFB1还降低了和的相对表达,而以剂量依赖性方式上调。AFB1诱导的脂质和脂蛋白代谢基因表达失调可能是将AFB1与脂质代谢改变以及最终冠心病风险联系起来的一种机制。

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