Key result
Naringin pretreatment or post-treatment significantly reduced doxorubicin-induced lipid peroxidation and elevated glutathione, glutathione-s-transferase, catalase, and superoxide dismutase levels in mouse liver.
Why the study?
Does naringin reduce doxorubicin-induced oxidative stress in the liver of Swiss albino mice?
Does naringin reduce doxorubicin-induced oxidative stress in the liver of Swiss albino mice?
Answers are grounded in this paper and cite their sources.
Naringin pretreatment effectively mitigates doxorubicin-induced oxidative stress in the liver of mice, suggesting a potential protective role against chemotherapy toxicity.
Doxorubicin a photosensitive antibiotic is frequently used to treat various malignancies in clinics; however, doxorubicin is also taken up by the normal cells of the body leading to increased oxidative stress and subsequently DNA damage and dysfunction in the cells. The agents which can reduce the adverse effect of doxorubicin will of great value. The present study has attempted to study the effect of naringin a citrus flavonoid on the doxorubicininduced oxidative stress in mice liver. The mice were administered with 0, 1, 5 or 10mg/ kg body weight of doxorubicin and treated with 10mg/kg body weight of naringin before or after doxorubicin treatment. The glutathione concentration and lipid peroxidation and activities of glutathione-s-transferase, catalase and super oxide dismutase were studied at 0.5, 1, 2 and 4h post-treatment in the mouse liver. The doxorubicin increased the lipid peroxidation in a dose dependent manner at all the post treatment times. Conversely, it attenuated the activities of glutathione-s-transferase, catalase and super oxide dismutase in dose dependent fashion and time dependent manner. A similar effect was observed for glutathione concentration. Treatment of mice with naringin before or after doxorubicin treatment elevated all the antioxidants and reduced the doxorubicin -induced lipid peroxidation. The effect of naringin pretreatment was more effective when compared to its post treatment. The naringin was very effective in reducing the oxidative stress induced by doxorubicin as indicated by the elevated levels of glutathione concentration, glutathiones-transferase, catalase and super oxide dismutase. The pretreatment of naringin was better than its post treatment.
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Ganesh Chandra Jagetia (2017) studied Doxorubicin-induced oxidative stress. Naringin vs. Doxorubicin alone was evaluated on Oxidative stress markers (glutathione, GST, catalase, SOD, lipid peroxidation) (p=<0.05). Naringin pretreatment or post-treatment significantly reduced doxorubicin-induced lipid peroxidation and elevated glutathione, glutathione-s-transferase, catalase, and superoxide dismutase levels in mouse liver.
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