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Published on: January 7, 2013
Protective effect of Panax ginseng extract on cisplatin-induced AKI via downregulating cell death associated genes
Reza Alipanah-Moghadam1, Vahideh Aghamohammadi2, Sina Seifi1
1Department of Clinical Biochemistry, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran.
Abstract:
This study is designed to assess the effect of root extract of P. ginseng on kidney tissue injury attributed to cisplatin and its molecular mechanism involved in this process in the AKI rat model. Twenty-four male Wistar rats were randomly allocated into 4 experimental groups including: the control group, the cisplatin group, the extract 100 mg/kg group, and the extract 200 mg/kg group. The duration of the investigation was 7 days, and all rats except the control group received a single dose of 10 mg/kg cisplatin on the 4th day. Our findings exhibited a significant reduction in blood concentration of creatinine in extract groups compared to the cisplatin group. In the cisplatin group, severe renal histopathological alterations were observed compared to the control group. In extract groups, significantly less tissue damage was observed than in the cisplatin group. Ginseng extract 200 showed minimal tissue damage as compared to extract 100. The expression of p21, p27, p53, TIMP2, IGFBP7, and NF-κB decreased significantly in extract groups compared to the cisplatin group. Our findings displayed amelioration of cisplatin-induced AKI and dose-dependent decrease of the NF-κB gene expression and cell death-inducing genes by administration of P. ginseng extract.
Insights
Panax ginseng root extract protects against cisplatin-induced kidney injury in rats. This study shows reduced kidney damage and lower expression of key injury markers with ginseng treatment, offering a potential therapeutic approach.
Area of Science:
- Pharmacology
- Nephrology
- Natural Products
Background:
- Cisplatin is a widely used chemotherapy agent with significant nephrotoxicity.
- Acute kidney injury (AKI) induced by cisplatin poses a clinical challenge.
- Exploring natural compounds for protective effects against drug-induced organ damage is crucial.
Purpose of the Study:
- To evaluate the protective effects of Panax ginseng root extract against cisplatin-induced kidney injury in a rat model.
- To investigate the underlying molecular mechanisms of ginseng's nephroprotective action.
Main Methods:
- Wistar rats were divided into control, cisplatin, and two ginseng extract (100 mg/kg and 200 mg/kg) treatment groups.
- Cisplatin was administered to induce AKI, followed by treatment with ginseng extract.
- Renal function (creatinine levels), histopathology, and expression of key molecular markers (p21, p27, p53, TIMP2, IGFBP7, NF-κB) were assessed.
Main Results:
- Ginseng extract significantly reduced serum creatinine levels compared to the cisplatin group.
- Histopathological examination revealed reduced renal tissue damage in rats treated with ginseng extract.
- Expression of p21, p27, p53, TIMP2, IGFBP7, and NF-κB was significantly downregulated in ginseng-treated groups, indicating reduced cell death and inflammation.
- A dose-dependent effect was observed, with the 200 mg/kg extract showing greater protection.
Conclusions:
- Panax ginseng root extract demonstrates significant nephroprotective effects against cisplatin-induced AKI in rats.
- The protective mechanism involves the downregulation of NF-κB signaling pathway and cell death-inducing genes.
- Ginseng extract represents a promising therapeutic candidate for mitigating cisplatin nephrotoxicity.
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