Combined effects of a high-fat diet and chronic valproic acid treatment on hepatic steatosis and hepatotoxicity in rats

被引:32
作者
Zhang, Li-fang [1 ]
Liu, Ling-sheng [1 ]
Chu, Xiao-man [2 ]
Xie, Hao [1 ]
Cao, Li-juan [1 ]
Guo, Cen [1 ]
Ji-ye, A. [1 ]
Cao, Bei [1 ]
Li, Meng-jie [1 ]
Wang, Guang-ji [1 ]
Hao, Hai-ping [1 ]
机构
[1] China Pharmaceut Univ, Key Lab Drug Metab & Pharmacokinet, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
[2] Jinling Hosp, Dept Clin Pharmacol, Nanjing 210002, Peoples R China
基金
中国国家自然科学基金;
关键词
valproic acid; high-fat diet; drug diet interaction; non-alcoholic fatty liver disease; hepatotoxicity; tricarboxylic acid cycle; amino acid; free fatty acid; metabonomics; CHROMATOGRAPHY-MASS SPECTROMETRY; GENE-EXPRESSION PROFILES; LIVER-DISEASE; MITOCHONDRIAL-FUNCTION; METABOLISM; METABONOMICS; TOXICITY; PLASMA; CANCER; BIOMARKERS;
D O I
10.1038/aps.2013.135
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aim: To investigate the potential interactive effects of a high-fat diet (HFD) and valproic acid (VPA) on hepatic steatosis and hepatotoxicity in rats. Methods: Male SD rats were orally administered VPA (100 or 500 mg.kg(-1).d(-1)) combined with HFD or a standard diet for 8 weeks. Blood and liver samples were analyzed to determine lipid levels and hepatic function biomarkers using commercial kit assays. Low-molecular-weight compounds in serum, urine and bile samples were analyzed using a metabonomic approach based on GC/TOF-MS. Results: HFD alone induced extensive hepatocyte steatosis and edema in rats, while VPA alone did not cause significant liver lesions. VPA significantly aggravated HFD-induced accumulation of liver lipids, and caused additional spotty or piecemeal necrosis, accompanied by moderate infiltration of inflammatory cells in the liver. Metabonomic analysis of serum, urine and bile samples revealed that HFD significantly increased the levels of amino acids, free fatty acids (FFAs) and 3-hydroxy-butanoic acid, whereas VPA markedly decreased the levels of amino acids, FFAs and the intermediate products of the tricarboxylic acid cycle (TCA) compared with the control group. HFD aggravated VPA-induced inhibition on lipid and amino acid metabolism. Conclusion: HFD magnifies VPA-induced impairment of mitochondrial beta-oxidation of FFAs and TCA, thereby increases hepatic steatosis and hepatotoxicity. The results suggest the patients receiving VPA treatment should be advised to avoid eating HFD.
引用
收藏
页码:363 / 372
页数:10
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