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Published on: February 28, 2013
Evaluation of selected antidiabetics in cardiovascular complications associated with cancer cachexia
Vivek R Bora1, Dhruv Gohel2, Rajesh Singh2
1Department of Pharmacology, Institute of Pharmacy, Nirma University, Sarkhej- Gandhinagar Highway, Ahmedabad, Gujarat, 382481, India.
Abstract:
So far, the cardio-protective potential of antidiabetics is proved, but their effect on cardiovascular complications associated with cancer cachexia is not explored until now. Insulin resistance and glucose intolerance along with systemic inflammation are prominent in cachexia but the potential effect of antidiabetic agents especially those belonging to biguanide, DPP4 inhibitors and SGLT2 on the heart are not studied till now. In present study, the effect of metformin, vildagliptin, teneligliptin, dapagliflozin and empagliflozin on cardiovascular complications associated with cancer cachexia by using B16F1 induced metastatic cancer cachexia and urethane-induced cancer cachexia was studied. These antidiabetic agents proved to be beneficial against cachexia-induced atrophy of the heart, preserved ventricular weights, maintained cardiac hypertrophic index, preserved the wasting of cardiac muscles assessed by HE staining, Masson trichrome staining, periodic acid Schiff staining and picro-Sirius red staining. Altered cardiac gene expression was attenuated after treatment with selected antidiabetics, thus preventing cardiac atrophy. Also, antidiabetic agents treatment improved the serum creatinine kinase MB, Sodium potassium ATPase and collagen in the heart. Reduction in blood pressure and heart rate was observed after treatment with antidiabetic agents. Results of our study show that the selected antidiabetics prove to be beneficial in attenuating the cardiac atrophy and helps in regulation of hemodynamic stauts in cancer cachexia-induced cardiovascular complications. Our study provides some direction towards use of selected antidiabetic agents in the management of cardiovascular complications associated with cancer cachexia and the study outcomes can be useful in desiging clinical trials.
Insights
Antidiabetic drugs like metformin and SGLT2 inhibitors protect the heart from cancer cachexia complications. These agents prevent cardiac atrophy and regulate hemodynamic status, offering potential therapeutic benefits.
Area of Science:
- Cardiovascular Research
- Endocrinology
- Oncology
Background:
- Cardio-protective effects of antidiabetics are known, but their impact on cancer cachexia-related cardiovascular issues remains unexplored.
- Cancer cachexia involves insulin resistance, glucose intolerance, and inflammation, potentially affecting cardiac health.
Purpose of the Study:
- To investigate the effects of biguanides, DPP4 inhibitors, and SGLT2 inhibitors on cardiovascular complications in cancer cachexia.
- To evaluate the efficacy of metformin, vildagliptin, teneligliptin, dapagliflozin, and empagliflozin in mitigating cardiac damage associated with cancer cachexia.
Main Methods:
- Utilized B16F1-induced metastatic and urethane-induced cancer cachexia models in mice.
- Assessed cardiac morphology and function using histological staining (HE, Masson trichrome, PAS, picro-Sirius red) and biochemical markers.
- Monitored changes in cardiac gene expression, serum markers (creatinine kinase MB, Sodium-Potassium ATPase), blood pressure, and heart rate.
Main Results:
- Antidiabetic agents prevented cachexia-induced cardiac atrophy, preserved ventricular weight, and maintained cardiac hypertrophic index.
- Histological analysis confirmed preservation of cardiac muscle and reduced fibrosis.
- Treatment attenuated altered cardiac gene expression, improved cardiac biomarkers, and reduced blood pressure and heart rate.
Conclusions:
- Selected antidiabetic agents demonstrate significant benefits in combating cardiac atrophy and regulating hemodynamic status in cancer cachexia.
- These findings suggest a potential role for antidiabetics in managing cardiovascular complications associated with cancer cachexia, warranting further clinical investigation.
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