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首页> 外文期刊>Biotechnic and Histochemistry >Effects of iloprost and sildenafil treatment on elabela, apelin-13, nitric oxide, and total antioxidant and total oxidant status in experimental enzyme-positive acute coronary syndrome in rats
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Effects of iloprost and sildenafil treatment on elabela, apelin-13, nitric oxide, and total antioxidant and total oxidant status in experimental enzyme-positive acute coronary syndrome in rats

机译:伊洛普斯特和西地那非治疗对大鼠实验酶阳性急性冠状动脉综合征的Elabela,Apelin-13,一氧化氮和总抗氧化和总氧化剂状态的影响

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Despite significant advances in medicine, mortality due to cardiovascular disease is not yet preventable. We investigated the amounts of elabela (ELA) and apelin, synthesized by cardiomyocytes, and changes of these compounds in cardiac tissue and circulation after administration of iloprost (ILO) and sildenafil (SIL) in rats with induced myocardial ischemia (MI). We also investigated a connection with circulating troponin-I, creatine kinase (CK), creatine kinase-myocardial band (CK-MB) and nitric oxide (NO), and total anti-oxidant (TAS)/total oxidant status (TOS). We established eight study groups of five rats each. Group 1, sham, was given only physiologic serum; group 2, ILO; group 3, SIL; group 4, ILO + SIL; group 5, MI; group 6, MI + ILO; group 7, MI + SIL; group 8, MI + ILO + SIL. Troponin-I, CK, CK-MB and TAS-TOS were investigated using an autoanalyzer. NO, ELA and apelin were analyzed by ELISA. Tissue apelin and ELA expressions and localizations were determined by immunohistochemistry. The MI group compared to the control (sham) group showed that ELA, apelin, troponin-I, CK, CK-MB, NO and TOS levels were elevated significantly. Concentrations of these factors increased in MI, but decreased after ILO and SIL administration. The largest decrease of TOS was identified in the ILO + SIL group. ELA and apelin may be novel indicators of MI and administration of ILO and SIL, individually or together, may be useful for treating MI.
机译:尽管医学发生了显着进展,但由于心血管疾病引起的死亡率尚未预防。我们研究了由心肌细胞合成的Elabela(ELA)和阿贝林的量,以及在具有诱导心肌缺血(MI)的大鼠大鼠中施用ILOPROST(ILO)和Sildenafil(Sill)的心脏组织和循环中这些化合物的变化。我们还研究了与循环肌钙蛋白-I,肌酸激酶(CK),肌酸激酶 - 心肌带(CK-MB)和一氧化氮(NO)的连接的连接,以及总抗氧化剂(TAS)/总氧化剂状态(TOS)。我们建立了八个学习组,每组五个大鼠。第1组,假,只给予生理血清;第2组,国际劳工组织;第3组,SIL;第4组,iLO + SIL;第5组,MI;第6组,MI + ILO;第7组,Mi + Sil;第8组,MI + ILO + SIL。使用AutoAnalyzer调查肌钙蛋白-I,CK,CK-MB和TAS-TOS。不,ELA和Apelin被ELISA分析。通过免疫组织化学确定组织己素和ELA表达和本地化。 MI组与对照(SHAM)组相比表明,ELA,Apelin,肌钙蛋白-1,CK,CK-MB,NO和TOS水平显着提高。这些因素的浓度增加了MI,但在ILO和SIL管理后减少。在ILO + SIL组中鉴定了最大的TOS降低。 ELA和APELIN可以是MI和ILO和SIL的施用的新型指示剂,单独或在一起,可用于治疗MI。

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