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作 者:林令君[1] 王晓俐[2] 张绪洪[1] 吕晓霞[3] 田洪波[1] 朱艳丽[2]
机构地区:[1]山东大学附属省立医院心血管科,山东济南250021 [2]山东大学附属省立医院老年心血管科,山东济南250021 [3]山东大学附属省立医院中心实验室,山东济南250021
出 处:《湖南中医药大学学报》2012年第8期7-9,共3页Journal of Hunan University of Chinese Medicine
基 金:山东省自然科学基金(Y2006C129)
摘 要:目的研究不同浓度厄贝沙坦对血管紧张素Ⅱ(AngⅡ)诱导的人单核/巨噬细胞系(THP-1)凝集素样氧化低密度脂蛋白受体(LOX-1)mRNA和蛋白表达的影响,并探讨其可能的机制。方法 THP-1细胞经0.16μmoL/L佛波酯诱导分化后,将细胞分为3组:对照组、AngⅡ组、厄贝沙坦干预组,干预组分别加入不同浓度厄贝沙坦孵育2 h后,再加入AngⅡ1×10-6moL/L孵育24 h,用荧光定量PCR和细胞酶联免疫法检测(LOX-1)mRNA和蛋白表达。结果与对照组比较,Ang II可明显上调THP1细胞(LOX-1)mRNA和蛋白表达,差异有统计学意义(P<0.05)。不同浓度厄贝沙坦均能抑制(LOX-1)蛋白表达(P<0.05),并且随着厄贝沙坦浓度降低,抑制作用减低,即两者呈浓度依赖性。结论厄贝沙坦以浓度依赖方式抑制AngⅡ诱导的THP1细胞(LOX-1)mRNA和蛋白表达,减少巨噬细胞通过(LOX-1)途径的氧化低密度脂蛋白(oxLDL)摄入,影响泡沫细胞的发生、发展,发挥其抗动脉粥样硬化(AS)作用。Objective To investigate the influence of irbesartan on expression of lectin-like oxidized low-density lipoprotein receptor-1 mRNA and protein in cultured THP-1 cells Methods THP-1 cells were differentiated by incubation with 160nM PMA for 72 hours.The cells were divided into three groups:control group, Ang IIgroup and irbesartan intervention group. The intervention groups were first treated with several concentration irbesartan for 2 hours, then coincubated with Ang II 1 × 10^-6moL/L for 24h, Real time PCR and enzyme-linked immunosorbent assay technology were used to detect (LOX-1) mRNA and protein expression.Results Ang II induced the increase of THP-1 (LOX-1) mRNA and protein expression(P〈0.05). Several concentration irbesartan groups blocked Ang II-induced (LOX-1) mRNA and protein expression,The decrease in (LOX-1) expression was dependent on irbesartan concentration. Conclusion Irbesartan can blocke Ang II -induced(LOX-1) mRNA and protein expression in a concentration-dependent and reduce intake of macrophages on the oxidized low density lipoprotei via (LOX-1) pathway, affecting the foam cell development,exert their effect on anti-atherosclerosis.
关 键 词:厄贝沙坦 人单核/巨噬细胞系 凝集素样氧化低密度脂蛋白受体
分 类 号:R963[医药卫生—微生物与生化药学]
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