机构地区:[1]第三军医大学营养卫生学教研室重庆市食品安全与营养研究重点实验室,重庆400038
出 处:《中华预防医学杂志》2007年第4期271-276,共6页Chinese Journal of Preventive Medicine
基 金:国家自然科学基金(30500408);达能营养研究与实验基金(2004)
摘 要:目的探讨核受体基因表达在不同膳食脂肪酸影响大鼠乳腺癌发生中的作用。方法用8种不同膳食脂肪酸(饱和脂肪酸、单不饱和脂肪酸、n-6多不饱和脂肪酸、n-3多不饱和脂肪酸、1:1 n-6/n-3多不饱和脂肪酸、5:1 n-6/n-3多不饱和脂肪酸、10:1 n-6/n-3多不饱和脂肪酸、1:2:1饱和脂肪酸/单不饱和脂肪酸/多不饱和脂肪酸其中 n-6/n-3多不饱和脂肪酸1:1)喂养 SD 雌性幼年大鼠,采用50 mg/kg 的甲基亚硝基脲单次腹腔注射诱导大鼠乳腺癌发生,电镜观察大鼠乳腺细胞结构变化,BrdU 体内标记法检测大鼠乳腺细胞增殖活性,RT-PCR 分析乳腺组织过氧化物酶增殖活化受体(PPARB 和 PPARγ)mRNA 表达。结果无乳腺癌诱发的各对照和 n-3多不饱和脂肪酸诱癌组大鼠乳腺细胞超微结构正常,细胞增殖活性低。而有大鼠乳腺癌诱发的组织细胞内可见明显的腺癌标志,且高乳腺癌诱发的饱和脂肪酸、单不饱和脂肪酸、n-6多不饱和脂肪酸、5:1 n-6/n-3多不饱和脂肪酸、10:1 n-6/n-3多不饱和脂肪酸和1:2:1饱和脂肪酸/单不饱和脂肪酸/多不饱和脂肪酸喂养组大鼠乳腺细胞增殖活性升高(BrdU 阳性率为21%~22%),但1:1 n-6/n-3多不饱和脂肪酸低诱癌组乳腺细胞增殖活性明显降低上述高乳腺癌诱发组(BrdU 阳性率为13%,P<0.05)。此外,过氧化物酶增殖活化受体作为与脂代谢密切相关的细胞核受体基因,1:1 n-6/n-3多不饱和脂肪酸低诱癌组较相应对照组上调 PPARβ和 PPARγmRNA 表达力度明显弱于高乳腺癌诱发组。结论不同膳食脂肪酸对 PPAR 基因表达的调节截然不同,这可能是差异性调节大鼠乳腺癌发生的分子机制之一。Objective To study the effects of different dietary fatty acid on the expression of nuclear receptor genes in the breast cancer of rats. Methods Fifty-day-old female Sprangue-Dawley rats were fed on eight different diets containing following fatty acids : saturated fatty acid ( SFA ) ; monounsaturated fatty acid (MUFA) ; n-6 polyunsaturated fatty acid (PUFA) ; n-3 PUFA ; 1 : 1 n-6/n-3 ; 5:1 n-6/n-3 ; 10:1 n-6/ n-3 ; 1 : 2 : 1 S/M/P ( n-6/n-3 at 1 : 1 ). The rats were given a single intraperitoneal injection of methyl- nitrosourea (MNU) at 50 mg/kg body weight to establish the rat model of mammary carcinogenesis, the ultrastructure changes of mammary gland cells in rats were observed by transmission electron microscope, the cell proliferation activity was detected by BrdU-labeld immunocytochemistry, and the expression of PPARβ and PPARγ mRNA were assayed by RT-PCR. Results There was no breast cancer occurring in control groups and the MNU-treated n-3 PUFA group, and the uhrastructure and proliferation activity of mammary gland cells in these groups were normal. In contrast, there appeared obvious marker of adenocarcinomas in mammary gland cells of MNU-induced breast cancer, and a high cell proliferation activity was found in tumor growth-enhancing groups (SFA, MUFA, n-6 PUFA, 5:1 n-6/n-3, 10:1 n-6/n-3 and S/M/P, 21%--22% of BrdU-labeled cells) , while a low cell proliferation activity was detected in rats fed with 1:1 n-6/n-3 diet ( 13% of BrdU-labeled cells, P 〈 0. 05 ). Moreover, peroxisome proliferator-activated receptors ( PPARs ),as important nuclear receptor genes of relating lipid metabolism, the expressions of PPARβ and PPARγ mRNA were significantly up-regulated in mammary adipose tissues of MNU-induced breast cancer as compared with the control groups, but the expression levels of peroxisome proliferator-activated receptors (PPARs) in rats fed with 1:1 n-6/n-3 group were lowest (P 〈 0. 05 ). Conclusion The different dietary fatty acid
关 键 词:膳食 脂肪酸类 乳腺肿瘤 胰岛素样生长因子Ⅱ 过氧化酶体激增剂 基因表达调控 大鼠 Sprague-Dawley
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