Impact of omega 3 alone or in combination with irinotecan on bone marrow and spleen of rats: in vivo study

Alaa H. Radhi, N. Al-Shawi, A. Hassan
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Abstract

Abstract Objectives: The present study designed to explore the genotoxicity through measurement of Mitotic index in bone marrow and the spleen cells, as possible mechanism of bone marrow and spleen toxicity that induced by irinotecan; and to describe the protective actions of omega 3 against irinotecan induced genotoxicity in bone marrow and the spleen of rats. Methods: Twenty four (24) rats (Sprague-Dawley) were randomly divided into four groups: Group Ӏ, rats  received single oral daily dose of distilled water (2 ml/kg) for 25 days (negative control group); Group ӀӀ (irinotecan-treated), received single daily oral dose of (2 ml/kg) distilled water for 25 days by the oral gavage and subsequently received irinotecan (50mg/kg) on days: 5, 10, 15 (total dose=150 mg/kg) by intraperitoneal injection; Group ӀӀӀ, received oral dose of Omega-3 fish oil (600mg/kg/day) daily for 25 successive days by oral gavage (Omega-3 fish oil-treated); Group ӀV (Omega-3 fish oil + irinotecan), received oral dose of Omega-3 fish oil (600mg/ kg/ day) given daily for 25 successive days by oral gavage, and received subsequently irinotecan (50mg / kg body weight) on days: 5, 10, 15 (total dose=150 mg/kg) by intraperitoneal injection. Results: Mitotic index in the Bone Marrow and in the Spleen Cells were shown to be significantly decreased (p<0.05) in rats treated with irinotecan (group ІІ) compared to corresponding levels in the negative control group (Group I) of the rats; Orally administered Omega-3 fish oil with total cumulative dose of irinotecan (Group IV), resulted in significant elevation (P<0.05) of the Mitotic index in bone marrow and the spleen cells compared to corresponding levels in rats treated with irinotecan (group ІІ). Conclusion: Results of current study suggested that the administration of Omega-3 fish oil could be useful supplements that may alleviate irinotecan induced genotoxicity through the elevation of mitotic indices in bone marrow and the spleen cells of the rats; but, in mild level.  
omega - 3单独或联合伊立替康对大鼠骨髓和脾脏的影响:体内研究
摘要目的:通过测定伊立替康对小鼠骨髓和脾脏细胞的有丝分裂指数,探讨其遗传毒性,探讨伊立替康致小鼠骨髓和脾脏毒性的可能机制;并探讨欧米伽- 3对伊立替康致大鼠骨髓和脾脏遗传毒性的保护作用。方法:将24只大鼠(Sprague-Dawley)随机分为4组:Ӏ组,大鼠口服蒸馏水(2 ml/kg),连续25 d(阴性对照组);ӀӀ组(伊立替康治疗),每日单次口服(2 ml/kg)蒸馏水灌胃25 d,随后在第5、10、15天腹腔注射伊立替康(50mg/kg)(总剂量=150 mg/kg);ӀӀӀ组,每天口服Omega-3鱼油(600mg/kg/天),连续25天灌胃(Omega-3鱼油处理);ӀV组(Omega-3鱼油+伊立替康),每天口服Omega-3鱼油(600mg/ kg/天),连续25天灌胃,随后在第5、10、15天腹腔注射伊立替康(50mg /kg体重)(总剂量= 150mg /kg)。结果:伊立替康治疗组(ІІ组)与阴性对照组(I组)相比,骨髓和脾脏细胞有丝分裂指数显著降低(p<0.05);口服Omega-3鱼油和伊立替康总累积剂量组(IV组),与伊立替康组(ІІ组)相比,骨髓和脾脏细胞有丝分裂指数显著升高(P<0.05)。结论:本研究提示Omega-3鱼油可通过提高大鼠骨髓和脾脏细胞有丝分裂指数来减轻伊立替康的遗传毒性;但是,在温和的水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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