Molecular Correlates of Early Onset of Diabetic Cardiomyopathy: Possible Therapeutic Targets.
Dongjuan WangKun LiuJinyan ZhongXin LiJie ZhangGongxin WangNi LiTianwen LiHarvey DavisIbrahim El-GabyGuoliang HaoHonghua YeDan LiPublished in: Oxidative medicine and cellular longevity (2022)
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.
Keyphrases
- high fat diet
- high glucose
- oxidative stress
- diabetic rats
- endothelial cells
- insulin resistance
- early onset
- left ventricular
- single cell
- adipose tissue
- type diabetes
- heart failure
- glycemic control
- fatty acid
- dna damage
- late onset
- rna seq
- gene expression
- cell death
- rheumatoid arthritis
- wound healing
- single molecule
- ischemia reperfusion injury
- polycystic ovary syndrome
- induced apoptosis
- signaling pathway
- cell cycle arrest
- genome wide
- high fat diet induced
- dna methylation
- diabetic nephropathy
- pluripotent stem cells