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三种钙拮抗剂冠状动脉内预处理增强猪心脏缺血耐受性的比较研究。

Comparative study on the enhancement of ischemic tolerance by intracoronary pretreatment with three calcium antagonists in pig hearts.

作者信息

Klein H H, Pich S, Lindert S, Nebendahl K, Kreuzer H

机构信息

Department of Cardiology, University of Göttingen, Federal Republic of Germany.

出版信息

Cardiovasc Drugs Ther. 1989 Jan;2(6):815-21. doi: 10.1007/BF00133213.

Abstract

The effect of intracoronary (IC) pretreatment with different calcium antagonists (diltiazem, nifedipine, verapamil) on the development of infarcts was investigated in two experimental series including 35 open-chest pigs. The left anterior descending coronary artery (LAD) was distally ligated for 75 minutes (series A) or for 45 minutes (series B) and was reperfused for 24 hours. Infarct size was determined as the ratio of infarcted myocardium (tetrazolium stain) to the risk region (dye technique). In series A, 20 pigs were pretreated immediately before occlusion with either IC diltiazem (n = 5, 4 mg/2 min), IC nifedipine (n = 5, 0.4 mg/2 min), IC verapamil (n = 5, 1 mg/2 min), or isotonic sodium chloride solution (n = 5). In series B, IC diltiazem (n = 5, 4 mg/2 min), IC verapamil (n = 5, 1 mg/2 min), or isotonic saline solution (n = 5) were administered 8 minutes prior to ischemia. The IC infusion of all calcium antagonists (series A) depressed left ventricular peak pressure, diastolic blood pressure, and dp/dt max and increased heart rate and coronary venous oxygen saturation. The development of infarcts was significantly delayed by IC diltiazem and IC verapamil. Mean infarct sizes (series A) amounted to 62% in the diltiazem group, 88% in the nifedipine group, 40% in the verapamil group, and 94% in the control group. In series B, where a time period of 8 minutes elapsed between pretreatment and induction of ischemia, mean infarct sizes after 45 minutes of ischemia and 24 hours of reperfusion amounted to 47% in the diltiazem group, 4% in the verapamil group, and 76% in control experiments.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在两个包含35只开胸猪的实验系列中,研究了冠状动脉内(IC)预先给予不同钙拮抗剂(地尔硫卓、硝苯地平、维拉帕米)对梗死灶形成的影响。左冠状动脉前降支(LAD)在远端结扎75分钟(A系列)或45分钟(B系列),然后再灌注24小时。梗死面积通过梗死心肌(四氮唑染色)与危险区域(染料技术)的比例来确定。在A系列中,20只猪在闭塞前立即接受冠状动脉内给予地尔硫卓(n = 5,4 mg/2分钟)、硝苯地平(n = 5,0.4 mg/2分钟)、维拉帕米(n = 5,1 mg/2分钟)或等渗氯化钠溶液(n = 5)。在B系列中,在缺血前8分钟给予冠状动脉内地尔硫卓(n = 5,4 mg/2分钟)、维拉帕米(n = 5,1 mg/2分钟)或等渗盐溶液(n = 5)。所有钙拮抗剂的冠状动脉内输注(A系列)均降低了左心室峰值压力、舒张压和dp/dt max,并增加了心率和冠状静脉血氧饱和度。冠状动脉内地尔硫卓和维拉帕米显著延迟了梗死灶的形成。地尔硫卓组(A系列)的平均梗死面积为62%,硝苯地平组为88%,维拉帕米组为40%,对照组为94%。在B系列中,预处理和缺血诱导之间间隔8分钟,缺血45分钟和再灌注24小时后的平均梗死面积在 地尔硫卓组为47%,维拉帕米组为4%,对照实验中为76%。(摘要截断于250字)

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