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作 者:陈章强[1] 胡申江[1] 陈乃云[1] 夏强[2] 沈岳良[2]
机构地区:[1]浙江大学医学院附属第一医院心内科,浙江杭州310003 [2]浙江大学医学院生理教研室,浙江杭州310031
出 处:《中国病理生理杂志》2005年第9期1802-1806,共5页Chinese Journal of Pathophysiology
基 金:国家教育部留学回国人员科研启动基金资助项目(No.1999-747)
摘 要:目的:观察糖尿病大鼠心肌电学变化特点,探讨环维黄杨星D(CVB-D)对糖尿病心肌电生理的影响。方法:以SD雄性大鼠尾静脉注射四氧嘧啶(alloxan,50mg.kg-1)复制糖尿病模型,选择以年龄相匹配的SD雄性大鼠作为对照组。2周后,记录大鼠体表心电图和右心室乳头肌跨膜电位,观察CVB-D对跨膜电位的影响。结果:糖尿病造模后第2周时,心率明显减慢于对照组,体表心电图QT间期和右室乳头肌动作电位时程(APD)各水平均明显长于对照组大鼠(P<0.01),而静息膜电位(RP)、动作电位幅度(APA)和超射值(OS)以及0期去极化最大速率(Vmax)均无明显变化。CVB-D具有剂量依赖效应,在13.3-63.3μmol.L-1范围内呈剂量依赖性地延长糖尿病大鼠和对照组大鼠APD30、APD50、APD70和APD90,对糖尿病大鼠APD延长作用更大。在33.3-63.3μmol.L-1浓度范围内,CVB-D呈剂量依赖性抑制糖尿病大鼠和对照组大鼠的静息电位(RP)、动作电位幅值(APA)和0期最大去极化速度(Vmax),但对糖尿病组抑制更大。研究结果还显示,CVB-D还具有时间依赖效应,当20μmol.L-1灌流心室肌10min后开始出现作用,对照组到40min左右作用达高峰,而糖尿病组40min后仍继续延长。结论:糖尿病大鼠右室乳头肌动作电位时程和QT间期明显延长。CVB-D可进一步延长糖尿病大鼠的APD,抑制其RP、APA、OS以及Vmax,作用较对照组明显。AIM: To investigate the electrophysiological changes of diabetic myocardium and effects of cyclovirobuxine D (CVB- D) on its electrophysiology. METHODS: Diabetes was induced in male SD rats, using a single injection of alloxan into tail vein. Untreated age- matched animals were used as controls. Animal electrocardiogram (ECG) was recorded by 2 weeks. Effects of CVB- D on isolated right ventricular papillary muscle from experimental diabetic rats and control group were observed by recording the transmembrane potentials with conventional glass microelectrodes. RESULTS:QT intervals in ECG and action potential duration (APD) at all levels were significantly lengthened in myocardium from week 2 of diabetes. Within the concentration of 13.3 - 63.3 μmol· L-^-1, CVB - D prologated APD of diabetes in dose - dependent manner and more than that of control. Within the concentration of 33.3 - 63.3 μmol· L-^-1, CVB - D depressed RP, APA, Vmax and OS of diabetes in dose - dependent way and more than that of control. In addition, CVB - D at concentration of 20 μmol· L-^-1 prologated APD in a time - dependent manner. The most prologation of APD was attairved about 40 min in control, while more than 40 min in diabetes. CONCLUSION: The results show that QT intervals in ECG and APD at all levels are significantly lengthened in myocardium from week 2 of diabetes. CVB - D prolongates APD and inhibits RP, APA, OS and Vmax more in d. iabetes than in control.
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