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

被引:32
作者
Gogoi, Bhaskarjyoti [1 ]
Chatterjee, Priyajit [2 ]
Mukherjee, Sandip [2 ]
Buragohain, Alak Kumar [1 ,3 ]
Bhattacharya, Samir [2 ]
Dasgupta, Suman [1 ]
机构
[1] Tezpur Univ, Dept Mol Biol & Biotechnol, Sonitpur 784028, Assam, India
[2] Visva Bharati Univ, Sch Life Sci, Dept Zool, Santini Ketan 731235, W Bengal, India
[3] Dibrugarh Univ, Dibrugarh 786004, Assam, India
关键词
SFA; Ferulic acid; Fetuin-A; Insulin receptor; Insulin resistance; PKC epsilon; CONGESTIVE-HEART-FAILURE; KINASE-C-EPSILON; ADIPOSE-TISSUE; ACID; MECHANISM; INHIBITION; EXPRESSION; HMGA1; TLR4; BETA;
D O I
10.1016/j.bbrc.2014.08.079
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 beta (IR beta) in skeletal muscle cells, this was affected due to the defects in high mobility group A1 (HMGA1) protein obtruded by phospho-PKC epsilon and that adversely affects IR beta mRNA expression. FRL blocked PKC epsilon activation and thereby permitted HMGA1 to activate IR beta 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. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:382 / 388
页数:7
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