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

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

  • Toxicol Rep. 2017 Jul 24:4:408-414. doi: 10.1016/j.toxrep.2017.07.006.
Oluwakemi Anuoluwapo Rotimi 1 Solomon Oladapo Rotimi 1 Chibueze Uchechukwu Duru 1 Ogheneworo Joel Ebebeinwe 1 Anthonia Obhio Abiodun 1 Boluwaji Oluwamayowa Oyeniyi 1 Francis Adedayo Faduyile 2
Affiliations

Affiliations

  • 1 Biochemistry Unit and Molecular Biology Research Laboratory, Department of Biological Sciences, Covenant University, Ota, Ogun State, Nigeria.
  • 2 Department of Pathology and Forensic Medicine, Lagos State University Teaching Hospital, Ikeja, Lagos, Nigeria.
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 Cpt1a 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 Ahr, Lipc and Lcat whereas, it upregulated Scarb1 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.

Keywords

Aflatoxin B1; Ahr, aryl hydrocarbon receptor; Cpt1a, carnitine palmitoyl transferase 1A; Gene expression; Lcat, lecithin – cholesterol acyltransferase; Lipc, hepatic lipoprotein lipase; Lipid; Lipoprotein; Liver; Scarb1, scavenger receptor class B member 1.

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