检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:李丽婷[1] 朱亦堃[1] 郗光霞[1] 史书红[1] 李兴[1] 赵宝珍[1]
机构地区:[1]山西医科大学第二医院内分泌科,太原030001
出 处:《中国药物与临床》2010年第8期858-861,共4页Chinese Remedies & Clinics
基 金:山西省卫生厅科技攻关计划项目(200911)
摘 要:目的观察不同浓度共轭亚油酸(c9,t11-CLA及t10,c12-CLA)干预后大鼠成骨细胞过氧化物酶体增殖物激活受体(PPAR)γ2及骨代谢相关基因核因子-κB活化受体配体(RANKL)、碱性磷酸酶(ALP)、骨保护素(OPG)mRNA表达水平的变化,探讨c9,t11-CLA及t10,c12-CLA对成骨细胞PPARγ2及骨代谢相关基因表达的影响。方法体外培养大鼠成骨细胞,分别加入c9,t11-CLA和t10,c12-CLA(终浓度均为0、12.5、25、50μmol/L)干预24h后,反转录聚合酶链反应(PCR)法检测成骨细胞PPARγ2、RANKL、ALP、OPG mRNA表达水平,比较不同浓度c9,t11-CLA及t10,c12-CLA对上述基因表达的影响。组间比较采用单因素方差分析。结果①不同浓度c9,t11-CLA呈剂量依赖性上调成骨细胞RANKL、OPG mRNA的表达水平,组间比较差异有统计学意义(P<0.05,P<0.01);c9,t11-CLA上调ALP mRNA的表达水平与剂量无关,而其对PPARγ2 mRNA的表达影响不明显。②不同浓度t10,c12-CLA呈剂量依赖性上调RANKL和OPG mRNA的表达水平,组间比较差异有统计学意义(P<0.05,P<0.01);且呈非剂量依赖性上调ALPmRNA的表达,下调PPARγ2mRNA的表达,与对照组比较差异有统计学意义(P<0.05,P<0.01)。结论 c9,t11-CLA及t10,c12-CLA可能通过促进成骨细胞标记物基因表达有利于骨形成,可能为骨质疏松的治疗提供新思路。Objective To observe the effects of conjugated linoleic acids (c9,t11-CLA and t10,c12-CLA) at various dosage on mRNA expression of peroxisome proliferator activated receptorsγ2 (PPARγ2), receptor activator of NF-κB ligand (RANKL), alkaline phosphatase (ALP) and osteoprotegerin (OPG) of osteoblastic cells, and to study the effects of c9,t11-CLA and t10,c12-CLA on bone metabolism. Methods Osteoblastic cells of Wistar rats were cultured in vitro and the fourth generation cells were selected to be cultured with c9, t11-CLA or t10, c12-CLA at different concentrations (the final concentration was 0, 12.5, 25, 50μmol/L, respectively) for 24h. RT-PCR was performed to semi-quantitatively determine and compared the mRNA expression of PPARγ2, RANKL, ALP and OPG as affected by different levels of c9, t11-CLA and t10, c12-CLA. Results Semi-quantitative RT-PCR analysis showed that c9,t11- CLA up-regulated the mRNA expression of RANKL and OPG in a dose-dependent manner (P0.05, P0.01, by interclass comparison) as well as the ALP mRNA expression albeit in a non-dose-dependent manner, but had no effect on the mRNA expression of PPARγ2. t10,c12-CLA up-regulated the mRNA expression of RANKL and OPG in a dose- dependent manner (P0.05, P0.01, by interclass comparison) as well as the ALP mRNA expression albeit in a non- dose-dependent manner, but down-regulated the expression of PPARγ2 (P0.05, P0.01, compared with controls). Conclusion c9,t11-CLA and t10,c12-CLA may promote the expression of osteogenic genes and thereby facilitate osteogenesis. These findings tentatively suggested a possible beneficial effect on bone formation.
关 键 词:过氧化物酶体增殖物激活受体 亚油酸类 共扼 成骨细胞 骨质疏松
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:52.15.66.233