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多酚可挽救骨骼肌细胞和脂肪细胞中脂质诱导的胰岛素抵抗。

A polyphenol rescues lipid induced insulin resistance in skeletal muscle cells and adipocytes.

机构信息

Department of Molecular Biology and Biotechnology, Tezpur University, Tezpur 784028, Napaam, Sonitpur, Assam, India.

Department of Zoology, School of Life Science, Visva-Bharati University, Santiniketan 731235, West Bengal, India.

出版信息

Biochem Biophys Res Commun. 2014 Sep 26;452(3):382-8. doi: 10.1016/j.bbrc.2014.08.079. Epub 2014 Aug 23.

Abstract

Skeletal muscle and adipose tissues are known to be two important insulin target sites. Therefore, lipid induced insulin resistance in these tissues greatly contributes in the development of type 2 diabetes (T2D). Ferulic acid (FRL) purified from the leaves of Hibiscus mutabilis, showed impressive effects in preventing saturated fatty acid (SFA) induced defects in skeletal muscle cells. Impairment of insulin signaling molecules by SFA was significantly waived by FRL. SFA markedly reduced insulin receptor β (IRβ) in skeletal muscle cells, this was affected due to the defects in high mobility group A1 (HMGA1) protein obtruded by phospho-PKCε and that adversely affects IRβ mRNA expression. FRL blocked PKCε activation and thereby permitted HMGA1 to activate IRβ promoter which improved IR expression deficiency. In high fat diet (HFD) fed diabetic rats, FRL reduced blood glucose level and enhanced lipid uptake activity of adipocytes isolated from adipose tissue. Importantly, FRL suppressed fetuin-A (FetA) gene expression, that reduced circulatory FetA level and since FetA is involved in adipose tissue inflammation, a significant attenuation of proinflammatory cytokines occurred. Collectively, FRL exhibited certain unique features for preventing lipid induced insulin resistance and therefore promises a better therapeutic choice for T2D.

摘要

骨骼肌和脂肪组织是已知的两个重要的胰岛素靶位。因此,这些组织中脂质引起的胰岛素抵抗在 2 型糖尿病(T2D)的发展中起着重要作用。从木槿叶中纯化的阿魏酸(FRL)在预防饱和脂肪酸(SFA)引起的骨骼肌细胞缺陷方面显示出令人印象深刻的效果。FRL 显著减轻了 SFA 对胰岛素信号分子的损害。SFA 显著降低了骨骼肌细胞中的胰岛素受体 β(IRβ),这是由于高迁移率族蛋白 A1(HMGA1)蛋白的缺陷所致,这种缺陷是由磷酸化蛋白激酶 Cε(PKCε)引起的,而这又会对 IRβmRNA 的表达产生不利影响。FRL 阻断了 PKCε 的激活,从而允许 HMGA1 激活 IRβ启动子,从而改善了 IR 表达的不足。在高脂肪饮食(HFD)喂养的糖尿病大鼠中,FRL 降低了血糖水平,并增强了从脂肪组织中分离出的脂肪细胞的脂质摄取活性。重要的是,FRL 抑制了胎球蛋白-A(FetA)基因的表达,降低了循环 FetA 水平,因为 FetA 参与脂肪组织炎症,因此促炎细胞因子的水平显著降低。总之,FRL 表现出预防脂质诱导的胰岛素抵抗的某些独特特征,因此有望成为 T2D 的更好治疗选择。

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