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作 者:张媛[1] 徐红[1] 杨汝春[1] 周法根[1] 侯小青[2]
机构地区:[1]浙江中医药大学附属广兴医院,杭州310007 [2]浙江中医药大学
出 处:《浙江中西医结合杂志》2013年第4期259-261,共3页Zhejiang Journal of Integrated Traditional Chinese and Western Medicine
基 金:浙江省中医药科研计划项目(No.2008CA080)
摘 要:目的:观察复方芪苓无糖颗粒对高脂损伤血管内皮细胞的保护作用,探讨其治疗高脂血症的作用机制。方法:用高脂血清造成人血管内皮细胞(EVC)损伤模型,以复方芪苓无糖颗粒及血脂康含药血清进行干预。光镜下观察细胞形态变化,MTT法检测细胞活性;采用逆转录-聚合酶链反应(RT-PCR)技术检测复方芪苓无糖颗粒高、中、低剂量各组对高脂血清诱导的血管内皮细胞表面黏附分子(TGF-β1)基因表达。结果:复方芪苓无糖颗粒各剂量组及血脂康组均能使高脂损伤的EVC形态趋于正常,活性增强,细胞膜损伤减轻;并均有上调内皮细胞TGF-β1的趋势,血脂康组TGF-β1表达与复方芪苓颗粒中、高浓度组比较无统计学意义(P>0.05)。结论:复方芪苓无糖颗粒对高脂损伤的血管内皮细胞有保护作用,可能是其防治高脂血症及动脉粥样硬化的作用机制之一。Objective: To study the protective effect of sugar-free Qiling compound granules on endothelial vascu- lar cells(EVC) against injuries by hyperlipidemic serum, in an attempt to understand the underlying mechanism of sugar-free Qiling compound granules in treating hyperlipidemia. Methods: Hyperlipidemic serum was used to establish injured model of EVC. Sera with sugar-free Qiling compound granules of low, medium, high concentra- tions and Xuezhikang were applied with hyperlipidemic serum together. The morphologic changes of EVC were ob- served under light microscope and EVC activity was determined by MTT method. Reverse transcription-poly- merase chain reaction(RT-PCR) technique was used to detect hyperlipidemia induced EVC surface adhesion mole- cule(TGF-β1) gene expression in 3 Qiling groups. Results: After treatment of 3 doses of Qiling compound and Xuezhikang, abnormal morphologic changes of EVC induced by hyperlipidemic serum gradually retained to nor- mal, the activity of EVC increased, and the injury of cell membrane lessened. The mRNA's expression of TGF-β1 in all groups increased after treatment and the expression was not statistically different between the Xuezhi- kang group and the sugar-free Qiling groups with medium and high concentrations(P〉0.05). Conclusion:Sug- ar-free Qiling compound granules have a protective effect on EVC against injuries induced by hyperlipidemic serum and can be used as prevention and treatment for hyperlipidemia and atherosclerosis ideal medication.
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