Related Experiment Video
Updated: Aug 15, 2026

Dioscin Mediated IgA Nephropathy Alleviation by Inhibiting B Cell Activation In Vivo and Decreasing Galactose-Deficient IgA1 Production In Vitro
Published on: October 13, 2023
Investigating the protective effects of aged garlic extract on cyclosporin-induced nephrotoxicity in rats
Orawan Wongmekiat1, Kamthorn Thamprasert
1Department of Physiology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand. wongmekiat_o@yahoo.co.uk
Abstract:
Cyclosporin A (CsA) nephrotoxicity has been described in solid organ recipients and in the patients who were treated for autoimmune diseases. Reactive oxygen species-induced oxidative stress and lipid peroxidations are implicated in the pathophysiology of CsA-induced renal injury. Aged garlic extract (AGE) has been reported to exhibit potent antioxidative and free radical scavenging abilities in various disease conditions. The present study was designed to investigate whether AGE could possibly have a protective effect against nephrotoxicity induced by CsA. Male Wistar rats were treated orally with CsA (50 mg/kg/day), CsA + AGE (0.25, 0.5, 1, and 2 g/kg/day started 3 days before the first dose of CsA), or the vehicle of CsA for a period of 10 days. Blood urea nitrogen, serum creatinine, creatinine clearance, and renal histopathological changes were evaluated after 24 h of the last treatment. CsA caused an increase in blood urea nitrogen and serum creatinine by 117 and 100%, respectively, whereas it decreased creatinine clearance by 78% compared with the vehicle-treated rats (all P < 0.001). AGE treatment (0.5, 1 and 2 g/kg) significantly protected animals against CsA-induced biochemical changes, albeit blood urea nitrogen and creatinine clearance in the 0.5 g/kg AGE treated-animals were only partially restored. Kidney sections taken from CsA-treated rats showed severe vacuolations and tubular necrosis. These histopathological changes were markedly improved by pretreatment of rats with AGE at the dose of 0.5--2 g/kg. The results indicate that AGE ameliorates renal dysfunction and morphological changes induced by CsA, and imply that it could be a beneficial remedy for attenuating the CsA nephrotoxicity.
Insights
Aged garlic extract (AGE) shows protective effects against cyclosporin A (CsA)-induced kidney damage. AGE treatment significantly improved kidney function and reduced harmful histological changes in rats, suggesting it may help prevent CsA nephrotoxicity.
Area of Science:
- Nephrology
- Pharmacology
- Toxicology
Background:
- Cyclosporin A (CsA) is known to cause kidney damage (nephrotoxicity), particularly in organ transplant recipients and those with autoimmune diseases.
- Oxidative stress and lipid peroxidation are key factors in the development of CsA-induced renal injury.
- Aged garlic extract (AGE) possesses antioxidant and free radical scavenging properties.
Purpose of the Study:
- To investigate the potential protective effects of Aged Garlic Extract (AGE) against Cyclosporin A (CsA)-induced nephrotoxicity.
- To evaluate the impact of AGE on biochemical markers and renal histopathology in a rat model of CsA nephrotoxicity.
Main Methods:
- Male Wistar rats were administered CsA (50 mg/kg/day) orally for 10 days.
- Rats received varying doses of AGE (0.25, 0.5, 1, and 2 g/kg/day) starting 3 days prior to CsA treatment.
- Kidney function was assessed by measuring blood urea nitrogen, serum creatinine, and creatinine clearance. Renal histopathology was also examined.
Main Results:
- CsA significantly increased blood urea nitrogen and serum creatinine, while decreasing creatinine clearance, indicating severe nephrotoxicity.
- AGE treatment at doses of 0.5, 1, and 2 g/kg significantly ameliorated these biochemical changes.
- Histopathological examination revealed that AGE (0.5-2 g/kg) markedly improved CsA-induced tubular necrosis and vacuolations.
Conclusions:
- Aged Garlic Extract (AGE) demonstrates a significant protective effect against Cyclosporin A (CsA)-induced nephrotoxicity in rats.
- AGE treatment improved kidney function and reduced structural damage caused by CsA.
- These findings suggest that AGE could be a beneficial therapeutic agent for mitigating CsA-induced renal injury.
