机构地区:[1]Central Clinical Laboratory, Affiliated Hospital of Hainan Medical University [2]Department of Cardiology Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology [3]Department of Physiology, Hainan Medical University
出 处:《Journal of Huazhong University of Science and Technology(Medical Sciences)》2015年第1期21-27,共7页华中科技大学学报(医学英德文版)
摘 要:The chronic effects of carboxyl-terminal polypeptide of Cardiotrophin-1(CT-1-CP) on ventricular electrical remodeling were investigated. CT-1-CP, which contains 16 amino acids in sequence of the C-terminal of Cardiotrophin-1, was selected and synthesized, and then administered to Kunming mice(aged 5 weeks) by intraperitoneal injection(500 ng·g^-1·day^-1)(4 groups, n=10 and female: male=1:1 in each group) for 1, 2, 3 and 4 weeks, respectively. The control group(n=10, female:male=1:1) was injected by physiological saline for 4 weeks. The epicardial monophasic action potential(MAP) was recorded by using a contact-type MAP electrode placed vertically on the left ventricular(LV) epicardium surface, and the electrocardiogram(ECG) signal in lead Ⅱ was monitored synchronously. ECG intervals(RR, PR, QRS and QT) and the amplitude of MAP(Am), the maximum upstroke velocity(Vmax), as well as action potential durations(APDs) at different repolarization levels(APD30, APD50, APD70, and APD90) of MAP were determined and analyzed in detail. There were no significant differences in RR and P intervals between CT-1-CP-treated groups and control group, but the PR segment and the QRS complex were greater in the former than in the latter(F=2.681 and 5.462 respectively, P〈0.05). Though QT interval and the corrected QT interval(QTc) were shorter in CT-1-CP-treated groups than in control group, the QT dispersion(QTd) of them was greater in the latter than in the former(F=3.090, P〈0.05) and increased with the time. The ECG monitoring synchronously with the MAP showed that the compression of MAP electrode on the left ventricular epicardium induced performance similar to myocardium ischemia. As compared with those before chest-opening, the PR segment and QT intervals remained basically unchanged in control group, but prolonged significantly in all CT-1-CP-treated groups and the prolongation of QT intervals increased gradually along with the time of exposure toThe chronic effects of carboxyl-terminal polypeptide of Cardiotrophin-1(CT-1-CP) on ventricular electrical remodeling were investigated. CT-1-CP, which contains 16 amino acids in sequence of the C-terminal of Cardiotrophin-1, was selected and synthesized, and then administered to Kunming mice(aged 5 weeks) by intraperitoneal injection(500 ng·g^-1·day^-1)(4 groups, n=10 and female: male=1:1 in each group) for 1, 2, 3 and 4 weeks, respectively. The control group(n=10, female:male=1:1) was injected by physiological saline for 4 weeks. The epicardial monophasic action potential(MAP) was recorded by using a contact-type MAP electrode placed vertically on the left ventricular(LV) epicardium surface, and the electrocardiogram(ECG) signal in lead Ⅱ was monitored synchronously. ECG intervals(RR, PR, QRS and QT) and the amplitude of MAP(Am), the maximum upstroke velocity(Vmax), as well as action potential durations(APDs) at different repolarization levels(APD30, APD50, APD70, and APD90) of MAP were determined and analyzed in detail. There were no significant differences in RR and P intervals between CT-1-CP-treated groups and control group, but the PR segment and the QRS complex were greater in the former than in the latter(F=2.681 and 5.462 respectively, P〈0.05). Though QT interval and the corrected QT interval(QTc) were shorter in CT-1-CP-treated groups than in control group, the QT dispersion(QTd) of them was greater in the latter than in the former(F=3.090, P〈0.05) and increased with the time. The ECG monitoring synchronously with the MAP showed that the compression of MAP electrode on the left ventricular epicardium induced performance similar to myocardium ischemia. As compared with those before chest-opening, the PR segment and QT intervals remained basically unchanged in control group, but prolonged significantly in all CT-1-CP-treated groups and the prolongation of QT intervals increased gradually along with the time of exposure to
关 键 词:carboxyl-terminal polypeptide of cardiotrophin-1 monophasic action potential action potential duration electrical remodeling
分 类 号:R541[医药卫生—心血管疾病]
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