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Updated: Oct 8, 2025

Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
Understanding diabetes-induced cardiomyopathy from the perspective of renin angiotensin aldosterone system
Vijayakumar Sukumaran1, Narasimman Gurusamy2, Huseyin C Yalcin3
1Biomedical Research Center, Qatar University, Al-Tarfa, 2371, Doha, Qatar. vijay@qu.edu.qa.
Insights
Diabetic cardiomyopathy (DCM) is a distinct heart dysfunction in diabetes. This review explores how the Renin Angiotensin Aldosterone System (RAAS) contributes to DCM, offering insights for better treatment strategies.
Area of Science:
- Cardiology
- Endocrinology
- Molecular Biology
Background:
- Diabetic cardiomyopathy (DCM) is a specific heart condition in individuals with diabetes mellitus (DM).
- DCM contributes significantly to heart failure and mortality, with increasing prevalence linked to rising DM rates.
- Current therapies for DCM are limited, despite its clinical importance.
Purpose of the Study:
- To review the role of the Renin Angiotensin Aldosterone System (RAAS) in the development of DCM.
- To elucidate the secondary cellular mechanisms, including inflammation, oxidative stress, mitochondrial dysfunction, and autophagy, mediated by RAAS in DCM.
- To identify gaps in current research on DCM and RAAS signaling.
Main Methods:
- Literature review of experimental and clinical studies on DCM and RAAS.
- Analysis of cellular pathways implicated in DCM pathogenesis.
- Identification of research areas requiring further investigation.
Main Results:
- RAAS plays a crucial role in DCM, independent of broader vascular complications.
- RAAS activation triggers secondary mechanisms like inflammation, oxidative stress, mitochondrial dysfunction, and altered autophagy in the heart.
- These RAAS-mediated pathways contribute to cardiomyocyte hypertrophy and diastolic dysfunction, characteristic of DCM.
Conclusions:
- Understanding the intricate role of RAAS in DCM is vital for developing effective therapeutic strategies.
- Targeting RAAS and its downstream pathways may offer new avenues for managing and treating diabetic cardiomyopathy.
- Further research is needed to fully elucidate RAAS signaling in DCM and optimize treatment outcomes.
Abstract:
Experimental and clinical evidence suggests that diabetic subjects are predisposed to a distinct cardiovascular dysfunction, known as diabetic cardiomyopathy (DCM), which could be an autonomous disease independent of concomitant micro and macrovascular disorders. DCM is one of the prominent causes of global morbidity and mortality and is on a rising trend with the increase in the prevalence of diabetes mellitus (DM). DCM is characterized by an early left ventricle diastolic dysfunction associated with the slow progression of cardiomyocyte hypertrophy leading to heart failure, which still has no effective therapy. Although the well-known "Renin Angiotensin Aldosterone System (RAAS)" inhibition is considered a gold-standard treatment in heart failure, its role in DCM is still unclear. At the cellular level of DCM, RAAS induces various secondary mechanisms, adding complications to poor prognosis and treatment of DCM. This review highlights the importance of RAAS signaling and its major secondary mechanisms involving inflammation, oxidative stress, mitochondrial dysfunction, and autophagy, their role in establishing DCM. In addition, studies lacking in the specific area of DCM are also highlighted. Therefore, understanding the complex role of RAAS in DCM may lead to the identification of better prognosis and therapeutic strategies in treating DCM.
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