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Expression of human apolipoprotein E4 reduces insulin-receptor substrate 1 expression and Akt phosphorylation in the ageing liver

机译:人载脂蛋白E4的表达降低衰老肝脏中胰岛素受体底物1的表达和Akt磷酸化

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The diabetic drug rosiglitazone was reported to improve glucose tolerance in insulin-resistant ApoE3 but not ApoE4 knock-in mice. We therefore examined whether apolipoprotein E (ApoE) has genotype-specific effects on liver insulin function. At 12weeks, no difference in liver insulin signaling was detected between fasting ApoE3 and ApoE4 mice. At 72weeks however, ApoE4 mice had lower IRS-1 and PI3K expression, and reduced Akt phosphorylation. This decline was associated with lower insulin and higher glucose in ApoE4 mouse liver. Liver cholesterol was not affected. These results show that ApoE4 expression reduces liver insulin signaling and insulin levels, leading to higher glucose content.
机译:据报道,糖尿病药物罗格列酮可改善胰岛素抵抗性ApoE3小鼠的葡萄糖耐量,但不能改善ApoE4敲入小鼠的葡萄糖耐量。因此,我们检查了载脂蛋白E(ApoE)是否对肝胰岛素功能具有基因型特异性作用。在第12周时,在空腹ApoE3和ApoE4小鼠之间未检测到肝胰岛素信号的差异。然而,在72周时,ApoE4小鼠的IRS-1和PI3K表达降低,并且Akt磷酸化降低。这种下降与ApoE4小鼠肝脏中较低的胰岛素和较高的葡萄糖相关。肝胆固醇未受影响。这些结果表明,ApoE4表达降低了肝脏胰岛素信号传导和胰岛素水平,从而导致更高的葡萄糖含量。

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