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Dapagliflozin: A Promising Strategy to Combat Cisplatin-Induced Hepatotoxicity in Wistar Rats
Shakta Mani Satyam1, Laxminarayana Kurady Bairy1, Abdul Rehman2
1Faculty of Pharmacology, RAK College of Medical Sciences, RAK Medical and Health Sciences University, Ras Al Khaimah 11172, United Arab Emirates.
Biology
|September 28, 2024
Summary
Dapagliflozin and silymarin show significant liver protection against cisplatin damage in rats. Combining these agents offers synergistic benefits, potentially reducing chemotherapy-induced liver injury.
Area of Science:
- Pharmacology
- Hepatology
- Oncology
Background:
- Chemotherapy, particularly cisplatin, causes significant hepatotoxicity.
- Drug repurposing and natural agents offer potential interventions for liver protection.
Purpose of the Study:
- To evaluate the hepatoprotective effects of dapagliflozin and silymarin against cisplatin-induced liver injury in a rat model.
- To investigate the potential synergistic effects of combining dapagliflozin and silymarin.
Main Methods:
- Adult female Wistar rats were divided into five groups and treated for 45 days.
- Treatments included cisplatin alone, silymarin, dapagliflozin, or a combination.
- Evaluations involved body weight, blood glucose, liver function tests, and histopathology.
Main Results:
- Cisplatin significantly elevated liver enzymes (ALT, AST, TB) and decreased protein/albumin.
- Dapagliflozin and silymarin administration significantly reduced liver enzymes and improved albumin levels.
- Combination therapy demonstrated synergistic effects, enhancing liver protection.
Conclusions:
- Dapagliflozin and silymarin exhibit substantial hepatoprotective properties against cisplatin-induced toxicity.
- Combination therapy shows synergistic potential for mitigating chemotherapy-related liver damage.
- Further research is needed for clinical translation in cancer patients.

