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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 的磷酸化。

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

机构信息

Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

出版信息

FEBS Open Bio. 2014 Feb 28;4:260-5. doi: 10.1016/j.fob.2014.02.011. eCollection 2014.

Abstract

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 12 weeks, no difference in liver insulin signaling was detected between fasting ApoE3 and ApoE4 mice. At 72 weeks 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.

摘要

糖尿病药物罗格列酮被报道能改善胰岛素抵抗的载脂蛋白 E3 而非载脂蛋白 E4 敲入小鼠的葡萄糖耐量。因此,我们研究了载脂蛋白 E(ApoE)是否对肝脏胰岛素功能具有基因型特异性影响。在 12 周时,空腹 ApoE3 和 ApoE4 小鼠之间的肝脏胰岛素信号没有差异。然而,在 72 周时,ApoE4 小鼠的 IRS-1 和 PI3K 表达降低,Akt 磷酸化减少。这种下降与 ApoE4 小鼠肝脏中的胰岛素和葡萄糖含量降低有关。肝脏胆固醇不受影响。这些结果表明,ApoE4 的表达降低了肝脏胰岛素信号和胰岛素水平,导致葡萄糖含量升高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9db7/3958919/a203f6917e14/gr1.jpg

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