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作 者:张奕[1] 林杰义[1] 罗玮[1] 黄少明[1] 毛丽梅[1]
机构地区:[1]南方医科大学公共卫生与热带医学学院营养与食品卫生学系,广州510515
出 处:《营养学报》2012年第2期128-131,134,共5页Acta Nutrimenta Sinica
基 金:国家自然科学基金(No.30571561);广东省"211工程"三期重点学科建设项目(No.GW201010);广东省高等学校人才引进项目资助
摘 要:目的探讨二十二碳六烯酸(docosahexaenoic acid,DHA)对3T3-L1脂肪细胞脂联素表达的影响及其机制。方法不同浓度DHA处理体外培养成熟的3T3-L1脂肪细胞,并选取一定浓度DHA加与不加过氧化物酶体增殖物激活受体γ(PPARγ)拮抗剂GW-9662处理脂肪细胞,实时荧光定量PCR分析处理前后脂联素基因和PPARγmRNA表达水平的差异。结果与对照组相比,当DHA浓度为50、100 mol/L时,脂联素表达水平分别增加71.89%、106.23%(P<0.05),随着浓度的增加脂联素表达降低,当DHA浓度达到400 mol/L时,脂联素表达水平最低(P<0.05)。当DHA浓度为100 mol/L时,脂肪细胞PPARγmRNA表达增加70.24%(P<0.05)。与对照组相比,DHA中加GW-9662处理组脂联素和PPARγmRNA表达水平分别降低97.32%、90.90%(P<0.05)。结论在一定浓度范围内,DHA对脂联素表达的影响呈剂量依赖关系,推测DHA可能是通过PPARγ途径调控脂肪细胞的脂联素表达。Objective To study the effects of docosahexaenoic acid on adiponectin mRNA and its mechanism in 3T3-l1 adipocytes.Method 3T3-L1 adipocytes were incubated with 25,50,100,200,400 μmol/L DHA,or with bull serum albumin(BSA) alone(control) for 24 h.Adipocytes were also incubated for 24 h with DHA plus GW-9662,a PPARγ antagonist,or with DHA alone.The mRNA expression of adiponectin and PPARγ was assessed by real-time fluorescence quantitative PCR.Result Both 50μmol/L and 100 μmol/L DHA increased(P0.05) the expression of adiponectin mRNA compared with the control(71.89% and 106.23% respectively),and the lowest was in group 400μmol/L(P0.05).The mRNA level of PPARγ in 100μmol/L group was significantly 70.24% higher as compared with the control(P0.05).Incubating with GW-9662 and DHA,decreases in the mRNA expression of adiponectin and PPARγ were 97.32% and 90.90%,compared with the control respectively.Conclusion DHA affects the expression of adiponectin mRNA in 3T3-L1 adipocytes concentration-dependently,possibly by a mechanism involving PPARγ.[ACTA NUTRIMENTA SINICA,2012,34(2):128-131,134]
关 键 词:二十二碳六烯酸 脂联素 3T3-L1脂肪细胞 过氧化物酶体增殖物激活受体Γ
分 类 号:R151.2[医药卫生—营养与食品卫生学]
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