The adiponectin signalling pathway - A therapeutic target for the cardiac complications of type 2 diabetes?

被引:36
作者
Sharma, Abhipree [1 ]
Mah, Michael [1 ]
Ritchie, Rebecca H. [1 ,2 ,3 ]
De Blasio, Miles J. [1 ,2 ]
机构
[1] Monash Univ, Monash Inst Pharmaceut Sci, Drug Discovery Biol, Heart Failure Pharmacol, Parkville, Vic 3052, Australia
[2] Monash Univ, Dept Pharmacol, Clayton, Vic 3800, Australia
[3] Monash Univ, Dept Med, Clayton, Vic 3800, Australia
关键词
Adiponectin receptors; Diabetes; Cardiomyopathy; Diastolic dysfunction; AMPK; PPAR alpha; ACTIVATED PROTEIN-KINASE; EPICARDIAL ADIPOSE-TISSUE; FATTY-ACID OXIDATION; DOXORUBICIN-INDUCED CARDIOTOXICITY; VENTRICULAR DIASTOLIC DYSFUNCTION; ISCHEMIA-REPERFUSION INJURY; OXYGEN SPECIES PRODUCTION; MOLECULE AMPK ACTIVATOR; PPAR-ALPHA; HEART-FAILURE;
D O I
10.1016/j.pharmthera.2021.108008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diabetes is associated with an increased risk of heart failure (HF). This is commonly termed diabetic cardiomyopathy and is often characterised by increased cardiac fibrosis, pathological hypertrophy, increased oxidative and endoplasmic reticulum stress as well as diastolic dysfunction. Adiponectin is a cardioprotective adipokine that is downregulated in settings of type 2 diabetes (12D) and obesity. Furthermore, both adiponectin receptors (AdipoR1 and R2) are also downregulated in these settings which further results in impaired cardiac adiponectin signalling and reduced cardioprotection. In many cardiac pathologies, adiponectin signalling has been shown to protect against cardiac remodelling and Iipotoxicity, however its cardioprotective actions in T2D-induced cardiomyopathy remain unresolved. Diabetic cardiomyopathy has historically lacked effective treatment options. In this review, we summarise the current evidence for links between the suppressed adiponectin signalling pathway and cardiac dysfunction, in diabetes. We describe adiponectin receptor-mediated signalling pathways that are normally associated with cardioprotection, as well as current and potential future therapeutic approaches that could target this pathway as possible interventions for diabetic cardiomyopathy. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页数:22
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