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PPARs modulate cardiac metabolism and mitochondrial function in diabetes.

作者信息

Lee Ting-Wei, Bai Kuan-Jen, Lee Ting-I, Chao Tze-Fan, Kao Yu-Hsun, Chen Yi-Jen

机构信息

Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, 250 Wu-Xing Street, Taipei, 11031, Taiwan.

Division of Endocrinology and Metabolism, Department of Internal Medicine, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan.

出版信息

J Biomed Sci. 2017 Jan 10;24(1):5. doi: 10.1186/s12929-016-0309-5.


DOI:10.1186/s12929-016-0309-5
PMID:28069019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5223385/
Abstract

Diabetic cardiomyopathy is a major complication of diabetes mellitus (DM). Currently, effective treatments for diabetic cardiomyopathy are limited. The pathophysiology of diabetic cardiomyopathy is complex, whereas mitochondrial dysfunction plays a vital role in the genesis of diabetic cardiomyopathy. Metabolic regulation targeting mitochondrial dysfunction is expected to be a reasonable strategy for treating diabetic cardiomyopathy. Peroxisome proliferator-activated receptors (PPARs) are master executors in regulating glucose and lipid homeostasis and also modulate mitochondrial function. However, synthetic PPAR agonists used for treating hyperlipidemia and DM have shown controversial effects on cardiovascular regulation. This article reviews our updated understanding of the beneficial and detrimental effects of PPARs on mitochondria in diabetic hearts.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63fb/5223385/f339365edb7e/12929_2016_309_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63fb/5223385/f339365edb7e/12929_2016_309_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63fb/5223385/f339365edb7e/12929_2016_309_Fig1_HTML.jpg

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本文引用的文献

[1]
HDAC Inhibition Modulates Cardiac PPARs and Fatty Acid Metabolism in Diabetic Cardiomyopathy.

PPAR Res. 2016

[2]
Fibrates inhibit the apoptosis of Batten disease lymphoblast cells via autophagy recovery and regulation of mitochondrial membrane potential.

In Vitro Cell Dev Biol Anim. 2016-3

[3]
Potential of vitamin D in treating diabetic cardiomyopathy.

Nutr Res. 2015-4

[4]
The mitochondria in diabetic heart failure: from pathogenesis to therapeutic promise.

Antioxid Redox Signal. 2015-6-10

[5]
Characterizing the mechanism of thiazolidinedione-induced hepatotoxicity: An in vitro model in mitochondria.

Toxicol Appl Pharmacol. 2015-4-15

[6]
H9c2 and HL-1 cells demonstrate distinct features of energy metabolism, mitochondrial function and sensitivity to hypoxia-reoxygenation.

Biochim Biophys Acta. 2015-2

[7]
Certain dietary patterns are beneficial for the metabolic syndrome: reviewing the evidence.

Nutr Res. 2014-7

[8]
Cardiac metabolism, inflammation, and peroxisome proliferator-activated receptors modulated by 1,25-dihydroxyvitamin D3 in diabetic rats.

Int J Cardiol. 2014-9

[9]
Myocardial contractile dysfunction is associated with impaired mitochondrial function and dynamics in type 2 diabetic but not in obese patients.

Circulation. 2014-6-13

[10]
The formation of brown adipose tissue induced by transgenic over-expression of PPARγ2.

Biochem Biophys Res Commun. 2014-3-15

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