Effects of Vitamin E and Q10 supplementation against doxorubicin-induced neurotoxicity in rats

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Abstract

Doxorubicin (DOX) is a chemotherapeutic agent; it is widely used in human malignancies. Its long-term use can cause neurobiological side-effects. Vitamin E and Coenzyme Q10 may possess neuroprotective effects. This work was designed to investigate the effect of vitamin E and the coenzyme Q10 (CoQ10) supplementation on neurotoxicity induced by doxorubicin (DOX) in rats. Forty nine adult rats of both sexes were used in this study; the animals were randomly enrolled into seven groups of 7 rats each. Group I: negative control (rats administered corn oil); Group II: Vitamin E at a dose of 100mg/kg/d for 3 weeks; Group III: CoQ10 at a dose of 50 mg/kg/d for 3 weeks; Group IV: positive control (Doxorubicin 2.5 mg/kg) every other day for 2 weeks; Group V: vitamin E at a dose of 100mg/kg/d for 3 weeks administered prior to Doxorubicin at dose 2.5 mg/kg every other day for 2 weeks; Group VI: CoQ10 at a dose of 50 mg/kg/d for 3 weeks administered prior to Doxorubicin at dose 2.5 mg/kg every other day for 2 weeks. Group VII: CoQ10 (50mg/kg/day), Vitamin E (100mg/kg) for 3 weeks administered prior to Doxorubicin at dose 2.5 mg/kg every other day for 2 weeks. On day twenty two of the study, brain of each animal was excised and part of it to be utilized to prepare homogenate for estimation interleukin-1 beta (IL-1β), and interleukin-10 (IL-10); the other part of brain was used for histological examination. Vitamin E and CoQ10 significantly (P<0.05) decreased IL-1beta, and only combination vitamin E and CoQ10 significantly (P<0.05) increased IL-10 and there was an improvement in the histopathological lesions of the brain in group V, group VI and group VII compared to group IV. In conclusion both Vitamin E and CoQ10 may have protective effect against DOX-induced neurotoxicity in rats.

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Al-Geam, M. A. I., & Al-Shawi, N. N. (2018). Effects of Vitamin E and Q10 supplementation against doxorubicin-induced neurotoxicity in rats. Iraqi Journal of Pharmaceutical Sciences, 27(2), 24–31. https://doi.org/10.31351/vol27iss2pp24-31

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