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首页> 外文期刊>The American Journal of the Medical Sciences >Response to a long-term high-fat diet in the signature of genes involved in lipid metabolism in ApoE-/- mice
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Response to a long-term high-fat diet in the signature of genes involved in lipid metabolism in ApoE-/- mice

机译:长期高脂饮食对ApoE-/-小鼠脂质代谢相关基因签名的反应

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摘要

High-fat diet (HFD)-induced lipid metabolism disorders are a critical feature of diet-induced insulin resistance (IR); however, the mechanisms underlying the tissue-specific effects of HFDs on the signature of genes involved in lipid metabolism have not been fully investigated. Glucose homeostasis and insulin sensitivity were monitored in chow-fed and HFD-fed ApoE mice using the hyperinsulinemic-euglycemic clamp technique. The signatures of genes involved in lipid metabolism were measured in the liver and adipose tissues by quantitative real-time polymerase chain reaction and Western blot analysis. Long-term HFD (for 16 weeks) resulted in marked abnormalities in glucose and lipid metabolism and induced IR in ApoE mice. Long-term HFD also markedly upregulated the messenger RNA (mRNA) expression of insulin-induced gene-2, sterol regulatory element-binding protein cleavage-activating protein and sterol regulatory element-binding protein-1 in the liver and/or adipose tissues, in parallel with an elevated insulin-induced gene-2 protein in the liver. However, HFD markedly downregulated the mRNA expression of sterol regulatory element-binding protein-2, 3-hydroxy-3-methylglutaryl coenzyme A reductase and low-density lipoprotein receptor in the liver. Interestingly, long-term HFD markedly decreased adipose triglyceride lipase and peroxisome proliferator-activated receptor-γ mRNA, and adipose triglyceride lipase protein contents in the liver and/or adipose tissues. These findings provide a framework to understand the mechanisms by which long-term HFD regulates the gene signatures involved in lipid metabolism in the pathogenesis of diet-induced IR.
机译:高脂饮食(HFD)引起的脂质代谢紊乱是饮食诱导的胰岛素抵抗(IR)的关键特征。然而,HFDs对脂质代谢相关基因签名的组织特异性作用的潜在机制尚未得到充分研究。使用高胰岛素-正常血糖钳夹技术,监测了由高脂饮食和HFD喂养的ApoE小鼠的葡萄糖稳态和胰岛素敏感性。通过实时定量聚合酶链反应和蛋白质印迹分析,在肝脏和脂肪组织中测量参与脂质代谢的基因的特征。长期HFD(持续16周)导致ApoE小鼠血糖和脂质代谢异常,并诱发IR。长期HFD还显着上调了肝脏和/或脂肪组织中胰岛素诱导的基因2,固醇调节元素结合蛋白裂解激活蛋白和固醇调节元素结合蛋白-1的信使RNA(mRNA)表达,与肝脏中胰岛素诱导的gene-2蛋白升高有关。然而,HFD显着下调了肝脏中固醇调节元件结合蛋白2、3-羟基-3-甲基戊二酰辅酶A还原酶和低密度脂蛋白受体的mRNA表达。有趣的是,长期的HFD明显降低了肝脏和/或脂肪组织中的甘油三酸酯脂肪酶和过氧化物酶体增殖物激活的受体-γmRNA,以及甘油三酸酯脂肪酶的蛋白质含量。这些发现提供了一个框架,以了解长期HFD调节饮食诱导的IR发病机理中涉及脂质代谢的基因标记的机制。

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