Affiliation:
1. Department of Biotechnology, Transcriptome Lab, Centre for Emerging Diseases, Jaypee Institute of Information
Technology, Noida, Sector- 62, Uttar Pradesh, India
Abstract
Background:
Diabetic cardiomyopathy has emerged as a major cause of cardiac fibrosis,
hypertrophy, diastolic dysfunction, and heart failure due to uncontrolled glucose metabolism in patients
with diabetes mellitus. However, there is still no consensus on the optimal treatment to prevent
or treat the cardiac burden associated with diabetes, which urges the development of dual antidiabetic
and cardioprotective cardiac therapy based on natural products. This study investigates the
cardiotoxic profile of glucose and the efficacy of AGE against glucose-induced cardiotoxicity in
H9c2 cardiomyocytes.
Methods:
The cellular metabolic activity of H9c2 cardiomyocytes under increasing glucose concentration
and the therapeutic efficacy of AGE were investigated using the MTT cell cytotoxicity assay.
The in vitro model was established in six groups known as 1. control, 2. cells treated with 25
μM glucose, 3. 100 μM glucose, 4. 25 μM glucose +35 μM AGE, 5. 100 μM glucose + 35 μM AGE,
and 6. 35 μM AGE. Morphological and nuclear analyses were performed using Giemsa, HE, DAPI,
and PI, respectively, whereas cell death was simultaneously assessed using the trypan blue assay. The
antioxidant potential of AGE was evaluated by DCFH-DA assay, NO, and H202 scavenging assay.
The activities of the antioxidant enzymes catalase and superoxide dismutase were also investigated.
The antiglycative potential of AGE was examined by antiglycation assays, amylase zymography, and
SDS PAGE. These results were then validated by in silico molecular docking and qRTPCR.
Results:
Hyperglycemia significantly reduced cellular metabolic activity of H9c2 cardiomyocytes,
and AGE was found to preserve cell viability approximately 2-fold by attenuating oxidative, fibrosis,
and apoptotic signaling molecules. In silico and qRTPCR studies confirmed that organosulfur
compounds target TNF-α, MAPK, TGF-β, MMP-7, and caspase-9 signaling molecules to ameliorate
glucose-induced cardiotoxicity.
Conclusion:
AGE was found to be an antidiabetic and cardioprotective natural product with exceptional
therapeutic potential for use as a novel herb-drug therapy in the treatment of diabetic cardiomyopathy
in future therapies.
Publisher
Bentham Science Publishers Ltd.
Subject
Cardiology and Cardiovascular Medicine,Pharmacology,Hematology
Cited by
2 articles.
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