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作 者:吴三五 徐欢 吴婷 WU San-wu;XU Huan;WU Ting(Department of Cardiology,The People's Hospital Affiliated of Hubei University of Medicine,Shiyan Hubei 442000,China)
机构地区:[1]湖北医药学院附属人民医院心血管内科
出 处:《临床和实验医学杂志》2019年第22期2385-2388,共4页Journal of Clinical and Experimental Medicine
基 金:十堰市医药卫生科技研究项目(编号:2016SY107)
摘 要:目的探讨尼可地尔(NIC)对大鼠冠状动脉微栓塞(CME)后心肌的影响及相关机制。方法48只SD大鼠随机分为3组:A组(假手术组)、B组(CME组)、C组(CME+NIC组),每组16只。B、C组建立CME模型,C组大鼠利用NIC溶于生理盐水,术前按照3mg/(kg·d)灌胃给药,A组和B组大鼠给以等量生理盐水。一周后取出各组大鼠心肌组织,TUNEL染色法观察心肌组织,流式细胞仪检测心肌细胞凋亡数量,实时定量荧光PCR及Westernblot检测NF-E2相关因子2(Nrf2)及血红素加氧酶1(HO-1)表达,酶联免疫吸附(ELISA)检测心肌组织Caspase-3表达。结果B组大鼠心肌凋亡细胞数显著高于A组,而C组显著低于B组,差异有统计学意义(P<0.05)。B组大鼠Nrf2及HO-1表达显著低于A组,而C组Nrf2及HO-1表达明显高于B组,差异有统计意义(P<0.05)。B组心肌组织Caspase-3表达显著高于A组,C组大鼠心肌组织Caspase-3表达显著低于B组,差异有统计学意义(P<0.05)。结论NIC可通过上调Nrf2/HO-1信号通路抑制CME后大鼠心肌细胞凋亡。Objective To explore the effects of nicorandil on myocardial apoptosis after coronary microembolization and to explore the potential mechanism.Methods 48 SD rats were averagely divided into 3 groups,including group A(the sham group),group B(CEM group),and group C(CME+NIC group).Apoptotic cells were observed by TUNEL method and flow cytometry at 7th day.Nrf2 and HO-1 expression were detected by real-time PCR and western blot.Meanwhile,the caspase-3 activity was valued by elisa.Results Apoptotic cells in group B were significantly higher than those in group A,while those in group C were markedly lower than those in group B(P<0.05).Nrf2 and HO-1 expression in group B were significantly lower than those in group A,and which in group C were effectively higher than those in group B(P<0.05).Besides,caspase-3 expression in group B was markedly higer than that in group A,and which in group C was significantly lower than that in group B(P<0.05).Conclusion Nicorandil could protect myocardial apoptosis after coronary microembolization probably via Nrf2/HO-1 pathway.
分 类 号:R541.4[医药卫生—心血管疾病] R-332[医药卫生—内科学]
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