Key result
Fullerenol pretreatment before doxorubicin administration decreased erythrocyte antioxidative capacity, with 50 mg/kg being insufficient for protection and 200 mg/kg potentially toxic.
Why the study?
Does fullerenol pretreatment prevent doxorubicin-induced oxidative stress in the blood of rats?
Does fullerenol pretreatment prevent doxorubicin-induced oxidative stress in the blood of rats?
Fullerenol pretreatment does not appear to protect against doxorubicin-induced oxidative stress in rat erythrocytes and may be toxic at higher doses.
Fullerenol pretreatment fails to protect rat erythrocytes from doxorubicin oxidative stress and may be toxic at higher doses; leaves open its role in cardioprotection.
In earlier in vitro investigations, fullerenol was shown to have a strong antioxidative capability. The present study examined the role of fullerenol as a potential antioxidative protector for doxorubicin-induced oxidative stress in the blood of rats through an investigation of the activity of glutathione-dependent enzymes (glutathione-S-transferase and glutathione peroxidase). It also assessed the influence of fullerenol on the number of blood cells (leukocytes and erythrocytes) as well as on the content of hemoglobin after a single dose administration of doxorubicin. Experiments were performed on six groups of adult male Wistar rats, each group containing eight individuals. Doxorubicin was administrated i.v. (tail vein) in a single dose of 10 mg/kg. Fullerenol C(60)(OH)(24) was administrated to the treated animals i.p. (in doses 50, 100, 200 mg/kg) 30 min before the dosing with doxorubicin. The control group animals were given saline (1 ml/kg; i.p.). One group of animals was treated only with fullerenol (100 mg/kg i.p.). The animals were sacrificed 2 and 14 days after the treatment. Each experiment was repeated twice. The results may indicate that fullerenol induces a decrease in the antioxidative capacity of erythrocytes in oxidative stress conditions, whereas, without doxorubicin, the application of fullerenol did not induce any changes in the enzyme activity of erythrocytes. The results of GST activity might indicate that 50 mg/kg are not sufficient to protect from doxorubicin toxicity, while 200 mg/kg might be toxic for animals, judging from the increase in GST activity.
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Torres et al. (2008) studied Doxorubicin-induced oxidative stress (n=48). Fullerenol C60(OH)24 vs. Saline or doxorubicin alone was evaluated on Activity of glutathione-dependent enzymes (glutathione-S-transferase and glutathione peroxidase). Fullerenol pretreatment before doxorubicin administration decreased erythrocyte antioxidative capacity, with 50 mg/kg being insufficient for protection and 200 mg/kg potentially toxic.
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