...
首页> 外文期刊>Cardiology >Effects of metoprolol on sympathetic remodeling and electrical remodeling at infarcted border zone after myocardial infarction in rabbits.
【24h】

Effects of metoprolol on sympathetic remodeling and electrical remodeling at infarcted border zone after myocardial infarction in rabbits.

机译:美托洛尔对兔心肌梗死后梗死边界区交感神经重塑和电重构的影响。

获取原文
获取原文并翻译 | 示例

摘要

BACKGROUND: The findings of sympathetic remodeling and its electrophysiological implications force us to rerecognize the drugs presently used. The aim of this study was to investigate the effects of metoprolol on sympathetic remodeling and electrical remodeling at the infarcted border zone (IBZ) after myocardial infarction (MI). METHODS: Forty rabbits were randomly assigned into two groups: MI group (n = 20), ligation of the anterior descending coronary; Metoprolol group (n = 20), ligation of the anterior descending coronary and administration of oral metoprolol 5 mg/kg/day. Eight weeks after surgery, transmural dispersion of repolarization (TDR) at baseline, TDR and difference of TDR (deltaTDR) during sympathetic nerve stimulation were measured at the IBZ. The distribution and densities of growth associated protein 43 and tyrosine hydroxylase positive nerves at the IBZ were detected with immunohistochemical techniques. RESULTS: The study was completed in the 36 surviving animals (18 rabbits in each group). The densities of growth associated protein 43 and tyrosine hydroxylase positive nerves in the Metoprolol group (2,550 +/- 554 and 1,779 +/- 458 microm2/mm2, respectively) were lower than in the MI group (3,217 +/- 589 and 2,616 +/- 528 microm2/mm2, respectively; both p < 0.01). TDR at baseline, TDR and deltaTDR during sympathetic nerve stimulation were shorter in the Metoprolol group than in the MI group (p < 0.01 for all). CONCLUSION: Metoprolol can inhibit sympathetic remodeling and electrical remodeling at the IBZ after MI. The association of metoprolol with improved electrical remodeling may be partly related to the inhibition of sympathetic remodeling.
机译:背景:交感神经重塑的发现及其电生理学意义迫使我们重新认识目前使用的药物。这项研究的目的是调查美托洛尔对心肌梗死(MI)后梗死边界区(IBZ)交感神经重塑和电重构的影响。方法:40只家兔随机分为两组:MI组(n = 20),结扎冠状动脉前降支;美托洛尔组(n = 20),结扎冠状动脉前降支并口服美托洛尔5 mg / kg /天。术后八周,在​​IBZ处测量基线时的跨膜弥散(TDR),交感神经刺激期间的TDR和TDR差异(deltaTDR)。用免疫组织化学技术检测IBZ上生长相关蛋白43和酪氨酸羟化酶阳性神经的分布和密度。结果:该研究在36只存活的动物(每组18只兔子)中完成。美托洛尔组的生长相关蛋白43和酪氨酸羟化酶阳性神经的密度(分别为2,550 +/- 554和1,779 +/- 458 microm2 / mm2)低于MI组(3,217 +/- 589和2,616 +分别为-/ 528微米/平方毫米;均p <0.01)。美托洛尔组的基线TDR,交感神经刺激期间的TDR和deltaTDR均比MI组短(所有p <0.01)。结论:美托洛尔可抑制心肌梗死后IBZ的交感重构和电重构。美托洛尔与改善的电重构的联系可能部分与交感神经重构的抑制有关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号