内科学
内分泌学
转录组
肉碱
生物
脂肪酸
脂肪生成
β氧化
脂肪酸代谢
脂质代谢
代谢组
过氧化物酶体
过氧化物酶体增殖物激活受体
二十碳五烯酸
脂联素
生物化学
多不饱和脂肪酸
非酒精性脂肪肝
微阵列分析技术
代谢组学
油酸
代谢综合征
脂肪肝
微阵列
CD36
甾醇调节元件结合蛋白
非诺贝特
脂肪变性
亚油酸
饱和脂肪酸
基因表达
肉碱棕榈酰转移酶I
胆固醇
作者
Zuoquan Xie,Houkai Li,Ke Wang,Jingchao Lin,Qi Wang,Guoping Zhao,Wei Jia,Qinghua Zhang
标识
DOI:10.1016/j.metabol.2009.08.022
摘要
Excessive energy intake greatly contributes to the development of nonalcoholic fatty liver disease (NAFLD) in modern society. To better understand the comprehensive mechanisms of NAFLD development, we investigated the metabolic alterations of rats with NAFLD induced by high-fat diet (HFD). Male Wistar rats were fed a HFD or standard chow for control. After 16 weeks, rat serum was collected for biochemical measurement. The rats' livers were resected and subjected to histology inspection and gene expression analysis with complementary DNA microarray and metabolic analysis with gas chromatography-mass spectroscopy. In HFD rats, the serum cholesterol, triglycerides, glucose, and insulin contents were increased; and the total cholesterol and triglycerides in the livers were also significantly increased. Complementary DNA microarray analysis revealed that 130 genes were regulated by HFD. Together with real-time reverse transcriptase polymerase chain reaction, lipid metabolism regulatory members like sterol regulatory element binding factor 1 and stearoyl-coenzyme A desaturase 1 had up-regulation, whereas others like peroxisome proliferator-activated receptor, carnitine palmitoyltransferase 1, and 3-hydroxy-3-methylglutaryl-coenzyme A reductase had repressed expression, in HFD rat livers. Metabolomic analysis showed that tetradecanoic acid, hexadecanoic acid, and oleic acid had elevation and arachidonic acid and eicosapentaenoic acid had decreased content in HFD rat livers. Amino acids including glycine, alanine, aspartic acid, glutamic acid, and proline contents were decreased. The integrative results from transcriptomic and metabolomic studies revealed that, in HFD rat livers, fatty acid utilization through beta-oxidation was inhibited and lipogenesis was enhanced. These observations facilitated our understanding of the pathways involved in the development of NAFLD induced by HFD.
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