Injac Rade, Perse Martina, Cerne Manica, Potocnik Nejka, Radic Natasa, Govedarica Biljana, Djordjevic Aleksandar, Cerar Anton, Strukelj Borut
Faculty of Pharmacy, Institute of Pharmaceutical Biology, University of Ljubljana, Askerceva 7, 1000 Ljubljana, Slovenia.
Biomaterials. 2009 Feb;30(6):1184-96. doi: 10.1016/j.biomaterials.2008.10.060. Epub 2008 Dec 1.
The effects of fullerenol C60(OH)24 (Frl) at doses of 25, 50, and 100mg/kg/week (for a time-span of 3 weeks) on heart and liver tissue after doxorubicin (Dox)-induced toxicity in rats with colorectal cancer were investigated. In the present study, we used an in vivo Wistar male rat model to explore whether Frl could protect against Dox-induced (1.5mg/kg/week for 3 weeks) chronic cardio- and hepato- toxicity and compared the effect with a well-known antioxidant, vitamin C (100mg/kg/week for 3 weeks). According to macroscopic, microscopic, hematological, biochemical, physiological, pharmacological, and pharmacokinetic results, we confirmed that, at all examined doses, Frl exhibits a protective influence on the heart and liver tissue against chronic toxicity induced by Dox.
研究了富勒醇C60(OH)24(Frl)以25、50和100mg/kg/周的剂量(持续3周)对结直肠癌大鼠阿霉素(Dox)诱导毒性后的心脏和肝脏组织的影响。在本研究中,我们使用体内Wistar雄性大鼠模型来探究Frl是否能预防Dox诱导的(1.5mg/kg/周,持续3周)慢性心脏和肝脏毒性,并将其效果与一种著名的抗氧化剂维生素C(100mg/kg/周,持续3周)进行比较。根据宏观、微观、血液学、生化、生理、药理学和药代动力学结果,我们证实,在所有检测剂量下,Frl对心脏和肝脏组织免受Dox诱导的慢性毒性均表现出保护作用。