Effect of conjugated linoleic acid on inhibition of prolyl hydroxylase 1 in hearts of mice

Lipids in Health and Disease

Research

Jize Zhang¹  Defa Li² 

[1] National Key Laboratory of Animal Nutrition, College Animal Science and Technology, China Agricultural University, 100193, Beijing, People's Republic of China;National Key Laboratory of Animal Nutrition, College Animal Science and Technology, China Agricultural University, 100193, Beijing, People's Republic of China;College Animal Science and Technology, 2-Yuan-Ming-Yuan West Rd., 100193, Beijing, Haidian District, China;

关键词: CLA;    HIF-2α;    PDK4;    PPARα;   

DOI  :  10.1186/1476-511X-11-22

 received in 2011-12-17, accepted in 2012-02-07,  发布年份 2012

来源: Springer

【 摘 要 】

BackgroundResults from different trails have provided evidence of protective effects of cis- 9,trans-11-conjugated linoleic acid (CLA) on cardiovascular diseases. But the inhibition of prolyl hydroxylase 1 (PHD1) associated with induction of hypoxia inducible factors (HIFs) by CLA in these protective effects has never been reported before. The objective of this study was to evaluate if the two predominant cis- 9,trans-11 (c9, t11), trans-10,cis-12 (t10, c12) CLA isomers and mixture of these two isomers can inhibit PHD1 with induction of HIFs in myocardium in mice and subsequent effects on myocardium metabolism.ResultsCLA mixture and c9, t11 CLA inhibited PHD1 protein expression and increased the levels of protein and mRNA in HIF-2α in myocardium in mice. Meanwhile, CLA mixture and c9, t11 CLA also elevated the expression of HIF related transcriptional factors like PDK4 and PPARα. The reprogramming of basal metabolism in myocardium in mice was shown on increasing of GLUT4 gene expression by c9, t11 CLA supplemented group. UCP2 was increased by CLA mixture and c9, t11 CLA for attenuating production of ROS.ConclusionCLA mixture and c9, t11 CLA could inhibit PHD1 and induce HIF-2α in myocardium in mice, which is associated with upregulation of PDK4 by activation of PPARα. This process also implies a reprogramming of basal metabolism and oxidative damage protection in myocardium in mice. All the effects shown in hearts of mice are due to c9, t11 CLA but not t10, c12 CLA.

【 授权许可】

CC BY   
© Zhang and Li; licensee BioMed Central Ltd. 2012