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鱼油(Maxepa)和 1α,25-二羟维生素 D(3)联合作用对 DMBA 诱导的大鼠乳腺癌发生的化学预防作用。

Combinatorial effect of fish oil (Maxepa) and 1alpha,25-dihydroxyvitamin D(3) in the chemoprevention of DMBA-induced mammary carcinogenesis in rats.

机构信息

Chemical Carcinogenesis and Chemoprevention Laboratory, Division of Biochemistry, Department of Pharmaceutical Technology, Jadavpur University, Calcutta (Kolkata) 700 032, West Bengal, India.

出版信息

Chem Biol Interact. 2010 Oct 6;188(1):102-10. doi: 10.1016/j.cbi.2010.06.007. Epub 2010 Jun 23.

Abstract

The present study demonstrates the anti-tumor effects of combined supplementations of dietary fish oil (Maxepa) and 1alpha,25-dihydroxyvitamin D(3) (vitamin D(3)) on 7,12-dimethylbenz(alpha)anthracene (DMBA)-induced rat mammary carcinogenesis. Female Sprague-Dawley rats at 50 days of age were treated with 7,12-dimethylbenz(alpha)anthracene (DMBA; 0.5mg/100g body weight) by a single tail vein injection in an oil emulsion. Both fish oil (rich in EPA and DHA) and vitamin D(3) were administered orally at a dose of 0.5 ml/day/rat and 0.3 microg/100 microL propylene glycol twice a week respectively and continued to 35 weeks after DMBA administration. Fish oil in combination with vitamin D(3) resulted in a significant reduction in incidence, multiplicity and volume of mammary tumors. These supplementation also inhibited DMBA-induced mammary 7-methylguanine DNA adducts formation, which was measured by HPLC-fluorescence assay (at four sequential time points; ANOVA, F=42.56, P<0.0001). Immunohistochemical analysis revealed that the effect of fish oil and vitamin D(3) occurred through suppression of cell proliferation (BrdU-LI: P<0.0001). Fish oil and vitamin D(3) together also reduced the mRNA expression of iNOS (84%, P<0.05). In view of their natural availability, non-toxicity and acceptability; combined supplementation of fish oil and vitamin D(3) might be effective for chemoprevention of mammary carcinogenesis.

摘要

本研究证实了联合补充膳食鱼油(Maxepa)和 1α,25-二羟维生素 D(3)(维生素 D(3))对 7,12-二甲基苯并(α)蒽(DMBA)诱导的大鼠乳腺肿瘤发生的抗肿瘤作用。50 天大的雌性 Sprague-Dawley 大鼠通过尾静脉注射油乳液中的 7,12-二甲基苯并(α)蒽(DMBA;0.5mg/100g 体重)进行处理。鱼油(富含 EPA 和 DHA)和维生素 D(3)分别以 0.5ml/天/大鼠和 0.3μg/100μL 丙二醇的剂量口服给药,每周两次,持续到 DMBA 给药后 35 周。鱼油与维生素 D(3)联合使用可显著降低乳腺肿瘤的发生率、多发性和体积。这些补充剂还抑制了 DMBA 诱导的乳腺 7-甲基鸟嘌呤 DNA 加合物的形成,这通过 HPLC-荧光测定法进行测量(在四个连续时间点;ANOVA,F=42.56,P<0.0001)。免疫组织化学分析显示,鱼油和维生素 D(3)的作用是通过抑制细胞增殖(BrdU-LI:P<0.0001)来实现的。鱼油和维生素 D(3)联合使用还降低了 iNOS 的 mRNA 表达(84%,P<0.05)。鉴于它们的天然可用性、非毒性和可接受性;联合补充鱼油和维生素 D(3)可能对乳腺肿瘤发生的化学预防有效。

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