Fish Oil Selectively Improves Heart Function in a Mouse Model of Lipid-induced Cardiomyopathy

被引:11
作者
Khan, Raffay S. [1 ]
Chokshi, Aalap [2 ]
Drosatos, Konstantinos [1 ]
Jiang, Hongfeng [1 ]
Yu, Shuiqing [1 ]
Harris, Collette R. [1 ]
Schulze, P. Christian [2 ]
Homma, Shunichi [2 ]
Blaner, William S. [1 ]
Shulman, Gerald I. [3 ]
Huang, Li-Shin [1 ]
Goldberg, Ira J. [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Div Prevent Med & Nutr, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Med, New York, NY 10032 USA
[3] Yale Univ, Sch Med, Dept Med, New Haven, CT 06510 USA
基金
美国国家卫生研究院;
关键词
heart failure; diabetes; lipotoxicity; omega; 3; fibrosis; POLYUNSATURATED FATTY-ACIDS; KINASE-C-BETA; LIPOTOXIC CARDIOMYOPATHY; DIABETIC CARDIOMYOPATHY; ACYL-CHAIN; ACTIVATION; INHIBITION; EXPRESSION; PRESSURE; MICE;
D O I
10.1097/FJC.0b013e318283d845
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Fish oil (FO) supplementation may improve cardiac function in some patients with heart failure, especially those with diabetes. To determine why this occurs, we studied the effects of FO in mice with heart failure either due to transgenic expression of the lipid uptake protein acyl CoA synthetase 1 (ACS1) or overexpression of the transcription factor peroxisomal proliferator-activated receptor (PPAR) gamma via the cardiac-specific myosin heavy chain (MHC) promoter. ACS1 mice and control littermates were fed 3 diets containing low-dose or high-dose FO or nonpurified diet (NPD) for 6 weeks. MHC-PPAR gamma mice were fed low-dose FO or NPD. Compared with control mice fed with NPD, ACS1, and MHC-PPARg, mice fed with NPD had reduced cardiac function and survival with cardiac fibrosis. In contrast, ACS1 mice fed with high-dose FO had better cardiac function, survival, and less myocardial fibrosis. FO increased eicosapentaenoic and docosahexaenoic acids and reduced saturated fatty acids in cardiac diacylglycerols. This was associated with reduced protein kinase C alpha and beta activation. In contrast, low-dose FO reduced MHC-PPAR gamma mice survival with no change in protein kinase C activation or cardiac function. Thus, dietary FO reverses fibrosis and improves cardiac function and survival of ACS1 mice but does not benefit all forms of lipid-mediated cardiomyopathy.
引用
收藏
页码:345 / 354
页数:10
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