Metabolic remodeling in chronic heart failure

被引:12
|
作者
Wang, Jing [1 ]
Guo, Tao [1 ]
机构
[1] Kunming Med Univ, Dept Cardiol, Affiliated Hosp 1, Kunming 650032, Peoples R China
来源
JOURNAL OF ZHEJIANG UNIVERSITY-SCIENCE B | 2013年 / 14卷 / 08期
关键词
Chronic heart failure (CHF); Metabolic remodeling; Metabolic substrate; Metabolic capability; FAILING HUMAN HEART; MYOCARDIAL FATTY-ACID; IDIOPATHIC DILATED CARDIOMYOPATHY; LEFT-VENTRICULAR DYSFUNCTION; ENERGY-METABOLISM; PGC-1; COACTIVATORS; SUBSTRATE METABOLISM; CARDIAC DYSFUNCTION; GLUCOSE-METABOLISM; OXIDATIVE STRESS;
D O I
10.1631/jzus.B1300137
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
Although the management of chronic heart failure (CHF) has made enormous progress over the past decades, CHF is still a tremendous medical and societal burden. Metabolic remodeling might play a crucial role in the pathophysiology of CHF. The characteristics and mechanisms of metabolic remodeling remained unclear, and the main hypothesis might include the changes in the availability of metabolic substrate and the decline of metabolic capability. In the early phases of the disease, metabolism shifts toward carbohydrate utilization from fatty acids (FAs) oxidation. Along with the progress of the disease, the increasing level of the hyperadrenergic state and insulin resistance cause the changes that shift back to a greater FA uptake and oxidation. In addition, a growing body of experimental and clinical evidence suggests that the improvement in the metabolic capability is likely to be more significant than the selection of the substrate.
引用
收藏
页码:688 / 695
页数:8
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