Molecular Correlates of Early Onset of Diabetic Cardiomyopathy: Possible Therapeutic Targets

Author:

Wang Dongjuan1ORCID,Liu Kun2ORCID,Zhong Jinyan1ORCID,Li Xin3ORCID,Zhang Jie3ORCID,Wang Gongxin4ORCID,Li Ni2ORCID,Li Tianwen5ORCID,Davis Harvey6ORCID,El-gaby Ibrahim2ORCID,Hao Guoliang24ORCID,Ye Honghua1ORCID,Li Dan2ORCID

Affiliation:

1. Department of Cardiology, HwaMei Hospital, University of Chinese Academy of Sciences, Ningbo, Zhejiang 315000, China

2. Burdon Sanderson Cardiac Science Centre and BHF Centre of Research Excellence, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, UK

3. Department of Endocrinology, HwaMei Hospital, University of Chinese Academy of Sciences, Ningbo, Zhejiang 315000, China

4. Henan SCOPE Research Institute of Electrophysiology Co. Ltd., Kaifeng 475000, China

5. Ningbo Institute of Life and Health Industry, University of Chinese Academy of Sciences, Ningbo, Zhejiang 315000, China

6. Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, UK

Abstract

Diabetes mellitus (DM) is associated with mitochondrial dysfunction and oxidative stress that can lead to diabetic cardiomyopathy (DCM), which can often remain undetected until late stages of the disease. However, myocardial injury occurs before the onset of measurable cardiac dysfunction, although its molecular correlates are poorly understood. In this study, we made a DM rat induced by a high-fat diet combined with low and high doses of streptozotocin (STZ) to emulate pre and early DCM. RNA-sequencing analysis of ventricular tissue revealed a differential transcriptome profile and abnormal activation of pathways involved in fatty acid metabolism, oxidative phosphorylation, cardiac structure and function, insulin resistance, calcium signalling, apoptosis, and TNF signalling. Moreover, using high glucose-treated human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CM), we recapitulated the cardiac cellular phenotype of DM and identified several molecular correlates that may promote the development of DCM. In conclusion, we have developed an experimental framework to target pathways underlying the progression of DCM.

Funder

Ningbo Health Branding Subject Fund

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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