The relationship of myocardial apoptosis and endoplasmic reticulum stressrelated protein CHOP in swine following coronary microembolization
LIN Chong-qiang1 LIU Tao2 TANG Zhong-li3 LIU Yang-chun4 LI Lang4
1.Department of Cardiovasolar Medicine,People′s Hospital of Cenxi City in Guangxi Zhuang Autonomous Region,Cenxi 543200,China;
2.Department of Cardiovasolar Medicine,Minzu Hospital of Guangxi Zhuang Autonomous Region,Nanning 530001,China;
3.DepartmentofCardiovasolarMedicine,People′sHospitalofDaoCountyinHunanProvince,DaoCounty 425300,China;
4.Department of Cardiology,the First Affiliated Hospital of Guangxi Medical University,Nanning 530001,China
Abstract:Objective To investigate the relation of myocardial apoptosis and endoplasmic reticulum stress-related(CME)protein C/EBP homologous protein (CHOP)in swine following coronary microembolization.Methods Fifty swine were selected and randomly divided into the Sham group (n=25)and the CME group (n=25).Five subgroups were assigned according to time points(3,6,12,24,48 h),5 cases in each group.The CME model was established through injecting microspheres into the coronary artery,while swine in the Sham group received the same dose of normal saline instead.Cardiac function was measured with echocardiography.Histopathological changes were detected with HE.Microinfarction and apoptotic index were detected with hematoxylinbasic fuchsinpicric acid (HBFP)and TUNEL stainings,respectively.The expressions of CHOP and Caspase-3 proteins were determined with Western blot.Results Compared with the Sham groups,the cardiac function was decreased in varying degrees in the corresponding CME groups(P<0.05).The cardiac function of 12 h following CME was the worst.Microinfarction rather than massive necrosis was found each time points following CME,mainly located in left ventricle and subendocardial myocardium.The difference,however,was not statistically significant(P>0.05).Compared with the Sham groups,the apoptotic index in the corresponding CME groups were increased in varying degrees(P<0.05).It peaked 12 h following CME.Apoptotic cardiomyocytes were mainly located in microinfarct area and its border area.Compared with the Sham groups,CHOP protein expression in the corresponding groups following CME enhanced in varying degrees(P<0.05),showing dynamic changes.It peaked 12 h following CME.Conclusion CME induces cardiomyocyte apoptosis and cardiac dysfunction,in which enhanced CHOP and caspase-3 expression may be involved.
林崇强;刘涛;唐中力;刘阳春;李浪. 猪冠状动脉微栓塞后心肌细胞凋亡与内质网应激相关蛋白CHOP表达的关系[J]. 中国当代医药, 2018, 25(12): 9-13.
LIN Chong-qiang;LIU Tao;TANG Zhong-li;LIU Yang-chun;LI Lang. The relationship of myocardial apoptosis and endoplasmic reticulum stressrelated protein CHOP in swine following coronary microembolization. 中国当代医药, 2018, 25(12): 9-13.
Chen ZW,Qian JY,Ma JY,et al.TNF-alpha-induced cardiomyocyte apoptosis contributes to cardiac dysfunction after coronary microembolization in mini-pigs[J].J Cell Mol Med,2014,18(10):1953-1963.
[7]
Wang J,Chen H,Zhou Y,et al.Atorvastatin inhibits myocardial apoptosis in a swine model of coronary microembolization by regulating PTEN/PI3K/Akt signaling pathway[J].Cell Physiol Biochem,2016,38(1):207-219.
[8]
Minamino T,Komuro I,Kitakaze M.Endoplasmic reticulum stress as a therapeutic target in cardiovascular disease[J].Circ Res,2010,107(9):1071-1082.
Jaffe R,Dick A,Strauss BH.Prevention and treatment of microvascular obstruction-related myocardial injury and coronary no-reflow following percutaneous coronary intervention:a systematic approach[J].JACC Cardiovasc Interv,2010,3(7):695-704.
[11]
Fokkema ML,Vlaar PJ,Svilaas T,et al.Incidence and clinical consequences of distal embolization on the coronary angiogram after percutaneous coronary intervention for ST-elevation myocardial infarction[J].Eur Heart J,2009,30(8):908-915.
[12]
Harrison RW,Aggarwal A,Ou FS,et al.Incidence and outcomes of no-reflow phenomenon during percutaneous coronary intervention among patients with acute myocardial infarction[J].Am J Cardiol,2013,111(2):178-184.
[13]
Charununtakorn ST,Shinlapawittayatorn K,Chattipakorn SC,et al.Potential roles of humanin on apoptosis in the heart[J].Cardiovasc Ther,2016,34(2):107-114.
[14]
Liu T,Zhou Y,Liu YC,et al.Coronary microembolization induces cardiomyocyte apoptosis through the LOX-1-dependent endoplasmic reticulum stress pathway involving JNK/P38 MAPK[J].Can J Cardiol,2015,31(10):1272-1281.
[16]
Minamino T,Kitakaze M.ER stress in cardiovascular disease[J].J Mol Cell Cardiol,2010,48(6):1105-1110.
[20]
Oyadomari S,Mori M.Roles of CHOP/GADD153 in endoplasmic reticulum stress[J].Cell Death Differ,2004,11(4):381-389.
[15]
Liu T,Zhou Y,Wang JY,et al.Coronary microembolization induces cardiomyocyte apoptosis in swine by activating the LOX-1-dependent mitochondrial pathway and caspase-8-dependent pathway[J].J Cardiovasc Pharmacol Ther,2016,21(2):209-218.
[17]
Hong D,Bai YP,Gao HC,et al.Ox-LDL induces endothelial cell apoptosis via the LOX-1-dependent endoplasmic reticulum stress pathway[J].Atherosclerosis,2014,235(2):310-317.