Medical Faculty, Department of Pharmacy, University of Novi Sad, Novi Sad, Serbia.
Toxicol Mech Methods. 2009 Jan;19(1):24-8. doi: 10.1080/01612840802203098.
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.
在早期的体外研究中,富勒醇表现出很强的抗氧化能力。本研究通过研究谷胱甘肽依赖酶(谷胱甘肽-S-转移酶和谷胱甘肽过氧化物酶)的活性,探讨了富勒醇作为潜在抗氧化保护剂在大鼠血液中对抗阿霉素诱导的氧化应激的作用。还评估了富勒醇对单次给予阿霉素后血细胞(白细胞和红细胞)数量以及血红蛋白含量的影响。实验在六组成年雄性 Wistar 大鼠上进行,每组包含八只个体。阿霉素经尾静脉(静脉内)单次注射 10 mg/kg。富勒醇 C(60)(OH)(24)经腹腔(在剂量 50、100、200 mg/kg 下)给药,在给予阿霉素前 30 分钟给予处理动物。对照组动物给予生理盐水(1 ml/kg;腹腔内)。一组动物仅用富勒醇(100 mg/kg 腹腔内)治疗。治疗后 2 天和 14 天处死动物。每个实验重复两次。结果可能表明,富勒醇在氧化应激条件下诱导红细胞抗氧化能力下降,而在没有阿霉素的情况下,富勒醇的应用不会引起红细胞酶活性的任何变化。GST 活性的结果可能表明,50 mg/kg 不足以防止阿霉素毒性,而 200 mg/kg 可能对动物有毒,从 GST 活性的增加可以判断。