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硫酸鱼精蛋白对左心室衰竭时心肌细胞收缩功能的不同影响。

Differential effects of protamine sulfate on myocyte contractile function with left ventricular failure.

作者信息

Hird R B, Crawford F A, Spinale F G

机构信息

Division of Cardiothoracic Surgery, Medical University of South Carolina, Charleston 29425.

出版信息

J Am Coll Cardiol. 1995 Mar 1;25(3):773-80. doi: 10.1016/0735-1097(94)00429-T.

Abstract

OBJECTIVES

This project tested two fundamental hypotheses: 1) Protamine sulfate has a direct and negative effect on myocyte contractile processes; 2) the negative effects of protamine on myocyte contractility will be enhanced in the setting of chronic left ventricular dysfunction.

BACKGROUND

An increasing number of patients undergoing cardiac and vascular surgical procedures have underlying chronic left ventricular dysfunction. Protamine sulfate is commonly required during these surgical procedures but has been associated with left ventricular dysfunction. However, it is not known whether protamine may have a direct and selective effect on myocyte contractility in the setting of chronic left ventricular dysfunction.

METHODS

This study examined the direct effects of protamine on isolated myocyte contractile function in 10 control pigs and 10 pigs with dilated cardiomyopathy induced by supraventricular tachycardia (rapid atrial pacing at 240 beats/min for 3 weeks). Myocyte contractile function was measured by videomicroscopy at baseline and with 10, 20, 40 or 80 micrograms/ml of protamine. In a second series of experiments, myocytes were preincubated with protamine and then stimulated with the beta-adrenergic agonist isoproterenol (25 nmol/liter).

RESULTS

In the presence of 20 micrograms/ml of protamine, myocyte contractile function was unaffected in the control group but decreased by 40% from baseline values in the supraventricular tachycardia group. With 10 micrograms/ml of protamine, myocyte beta-adrenergic responsiveness was reduced by 25% in the supraventricular tachycardia group with no change in the control group. In the presence of 40 and 80 micrograms/ml of protamine, myocyte contractile function decreased in both groups. However, 40 micrograms/ml of protamine caused a more pronounced decline in myocyte function and beta-adrenergic responsiveness in the supraventricular tachycardia group.

CONCLUSIONS

An increased sensitivity to the depressive effects of protamine on myocyte contractile function and beta-adrenergic responsiveness occurred in this model of chronic left ventricular dysfunction. These results suggest that patients with underlying cardiac disease may have an increased susceptibility to a sudden compromise of left ventricular contractile performance after protamine administration.

摘要

目的

本项目检验了两个基本假设:1)硫酸鱼精蛋白对心肌细胞收缩过程有直接负面影响;2)在慢性左心室功能障碍的情况下,鱼精蛋白对心肌细胞收缩性的负面影响会增强。

背景

越来越多接受心脏和血管外科手术的患者存在潜在的慢性左心室功能障碍。在这些外科手术过程中通常需要使用硫酸鱼精蛋白,但它与左心室功能障碍有关。然而,尚不清楚在慢性左心室功能障碍的情况下,鱼精蛋白是否可能对心肌细胞收缩性有直接和选择性的影响。

方法

本研究检测了鱼精蛋白对10只对照猪和10只因室上性心动过速(以240次/分钟的频率快速心房起搏3周)诱导的扩张型心肌病猪的离体心肌细胞收缩功能的直接影响。通过视频显微镜在基线以及使用10、20、40或80微克/毫升鱼精蛋白时测量心肌细胞收缩功能。在第二系列实验中,心肌细胞先用鱼精蛋白预孵育,然后用β-肾上腺素能激动剂异丙肾上腺素(25纳摩尔/升)刺激。

结果

在存在20微克/毫升鱼精蛋白的情况下,对照组心肌细胞收缩功能未受影响,但室上性心动过速组的心肌细胞收缩功能较基线值下降了40%。使用10微克/毫升鱼精蛋白时,室上性心动过速组心肌细胞的β-肾上腺素能反应性降低了25%,而对照组无变化。在存在40和80微克/毫升鱼精蛋白的情况下,两组心肌细胞收缩功能均下降。然而,40微克/毫升鱼精蛋白导致室上性心动过速组心肌细胞功能和β-肾上腺素能反应性下降更为明显。

结论

在这种慢性左心室功能障碍模型中,对鱼精蛋白对心肌细胞收缩功能和β-肾上腺素能反应性的抑制作用的敏感性增加。这些结果表明,患有潜在心脏病的患者在给予鱼精蛋白后,左心室收缩性能突然受损的易感性可能增加。

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