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作 者:王华强[1] 陈利国[2] 孙喜稳[3] 王盛飞[4] 李晴[5]
机构地区:[1]浙江省丽水市中医院,丽水323000 [2]暨南大学医学院,广州510632 [3]广州中医药大学中药学院,广州510006 [4]暨南大学附属第一医院东圃分院,广州510630 [5]广东省中医院,广州510120
出 处:《中华中医药杂志》2015年第12期4458-4461,共4页China Journal of Traditional Chinese Medicine and Pharmacy
基 金:国家自然科学基金项目(No.30572289);广东省自然科学基金项目(No.8151063201000060)~~
摘 要:目的:研究丹皮酚对高血压病血瘀证患者血清损伤后的血管内皮细胞(VEC)的膜联蛋白V与肌动蛋白结合的表达的影响,进一步探讨丹皮酚保护VEC的作用机制。方法:运用CCK-8法检测丹皮酚不同浓度25、50、100、250、500、1 000mg/L对人脐静脉内皮细胞活性的影响;选用250mg/L浓度的丹皮酚预干预细胞模型,运用免疫印记杂交技术检测丹皮酚组与对照组膜联蛋白V与肌动蛋白结合的表达。结果:丹皮酚不同浓度对细胞活性的影响:不同浓度组之间比较,差异无统计学意义。250mg/L丹皮酚干预后对与肌动蛋白结合的膜联蛋白V表达的影响:模型对照组、丹皮酚组与肌动蛋白结合的膜联蛋白V的表达逐渐降低,其中每组与肌动蛋白结合的膜联蛋白V的表达呈现血瘀证组、非血瘀证组、正常组逐渐降低的趋势。血瘀证组,丹皮酚组与模型对照组比较,差异有统计学意义(P<0.05)。结论:丹皮酚具有保护人脐静脉内皮细胞完整性的作用,其机制可能是通过降低肌动蛋白G/F含量比值的方式,减少膜联蛋白V与肌动蛋白的结合,促进肌动蛋白的重装。Objective: To study the inl uence of paeonol on the integrating expression of annexin V and actin ininjured vein endothelia cell(VEC)intervened with serum of hypertension patients with syndrome of blood stasis, and to investigate the action mechanism of paeonol in protecting VEC deeply. Methods: The inl uence of 25, 50, 100, 250, 500, 1 000mg/L paeonol onthe activity of human umbilical vein endothelia cell(HUVEC) was determined by CCK-8 method. The cell models were intervened with250mg/Lpaeonol, and the integrating expression of annexin V and actin of paeonol group and control group was tested by usingwestern blotting. Results: The inl uence of paeonol with different concentrations as 25, 50, 100, 250, 500, 1 000mg/L in cell activity had no statistical significance. The expression of annexin V integrated with actin of model group and 250mg/L paeonol group was decreased gradually, and the expression of annexin V integrated with actin showed a tendency of gradually decreased in syndrome of blood stasis group and followed by non-syndrome of blood stasis group and control group. The difference among syndrome of blood stasis group, paeonol group and model group had statistical significance(P0.05). Conclusion: Paeonol could protect the integrity of HUVEC through decreasing the content ration of G/F of action, reducing the combination ofannexin V and actin and promoting the reloading of actin.
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