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大型动物心肌梗死模型概述(综述)

Overview of large animal myocardial infarction models (review).

作者信息

Lukács E, Magyari B, Tóth L, Petrási Zs, Repa I, Koller A, Horváth Iván

机构信息

University of Pécs Heart Institute, Medical School Pécs Hungary.

出版信息

Acta Physiol Hung. 2012 Dec;99(4):365-81. doi: 10.1556/APhysiol.99.2012.4.1.

DOI:10.1556/APhysiol.99.2012.4.1
PMID:23238539
Abstract

There are several experimental models for the in vivo investigation of myocardial infarction (MI) in small (mouse, rat) and large animals (dog, pig, sheep and baboons). The application of large animal models raises ethical concerns, the design of experiments needs longer follow-up times, requiring proper breeding and housing conditions, therefore resulting in higher cost, than in vitro or small animal studies. On the other hand, the relevance of large animal models is very important, since they mostly resemble to human physiological and pathophysiological processes. The first main difference among MI models is the method of induction (open or closed chest, e.g. surgical or catheter based); the second main difference is the presence or absence of reperfusion. The former (i.e. reperfused MI) allows the investigation of reperfusion injury and new catheter based techniques during percutaneous coronary interventions, while the latter (i.e. nonreperfused MI) serves as a traditional coronary occlusion model, to test the effects of new pharmacological agents and biological therapies, as cell therapy. The reperfused and nonreperfused myocardial infarction has different outcomes, regarding left ventricular function, remodelling, subsequent heart failure, aneurysm formation and mortality. Our aim was to review the literature and report our findings regarding experimental MI models, regarding the differences among species, methods, reproducibility and interpretation.

摘要

有几种用于在小型(小鼠、大鼠)和大型动物(狗、猪、绵羊和狒狒)体内研究心肌梗死(MI)的实验模型。与体外或小型动物研究相比,大型动物模型的应用引发了伦理问题,实验设计需要更长的随访时间,需要适当的饲养和圈养条件,因此成本更高。另一方面,大型动物模型的相关性非常重要,因为它们大多类似于人类的生理和病理生理过程。MI模型之间的第一个主要区别是诱导方法(开胸或闭胸,例如手术或基于导管的);第二个主要区别是是否存在再灌注。前者(即再灌注MI)允许在经皮冠状动脉介入治疗期间研究再灌注损伤和新的基于导管的技术,而后者(即非再灌注MI)用作传统的冠状动脉闭塞模型,以测试新药理学药物和生物疗法(如细胞疗法)的效果。再灌注和非再灌注心肌梗死在左心室功能、重塑、随后的心力衰竭、动脉瘤形成和死亡率方面有不同的结果。我们的目的是回顾文献并报告我们关于实验性MI模型的发现,包括物种、方法、可重复性和解释方面的差异。

相似文献

1
Overview of large animal myocardial infarction models (review).大型动物心肌梗死模型概述(综述)
Acta Physiol Hung. 2012 Dec;99(4):365-81. doi: 10.1556/APhysiol.99.2012.4.1.
2
Myocardial infarction with and without reperfusion in sheep: early cardiac and neurohumoral changes.绵羊心肌梗死伴再灌注和不伴再灌注:早期心脏及神经体液变化
Clin Sci (Lond). 2000 Jun;98(6):703-11.
3
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Cardiovasc Pathol. 2006 Mar-Apr;15(2):83-90. doi: 10.1016/j.carpath.2005.10.006.
4
Minimally invasive close-chest method for creating reperfused or occlusive myocardial infarction in swine.用于在猪身上创建再灌注或闭塞性心肌梗死的微创闭胸方法。
Invest Radiol. 2005 Jan;40(1):14-8.
5
Effects of trimetazidine, a partial inhibitor of fatty acid oxidation, on ventricular function and survival after myocardial infarction and reperfusion in the rat.曲美他嗪,一种脂肪酸氧化部分抑制剂,对大鼠心肌梗死后再灌注心室功能和生存的影响。
Fundam Clin Pharmacol. 2010 Aug;24(4):469-76. doi: 10.1111/j.1472-8206.2009.00802.x. Epub 2009 Dec 17.
6
Impact of myocardial haemorrhage on left ventricular function and remodelling in patients with reperfused acute myocardial infarction.心肌出血对再灌注急性心肌梗死患者左心室功能及重构的影响。
Eur Heart J. 2009 Jun;30(12):1440-9. doi: 10.1093/eurheartj/ehp093. Epub 2009 Apr 3.
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The reduction of infarct size--forty years of research.梗死面积的缩小——四十年的研究
Rev Port Cardiol. 2010 Jun;29(6):1037-53.
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Antiarrhythmic effects of growth hormone--in vivo evidence from small-animal models of acute myocardial infarction and invasive electrophysiology.生长激素的抗心律失常作用——来自急性心肌梗死小动物模型和侵入性电生理学的体内证据
J Electrocardiol. 2008 Mar-Apr;41(2):144-51. doi: 10.1016/j.jelectrocard.2007.09.002.
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Embozene™ microspheres induced nonreperfused myocardial infarction in an experimental swine model.Embozene™ 微球诱导实验性猪模型发生非再灌注性心肌梗死。
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Midkine gene transfer after myocardial infarction in rats prevents remodelling and ameliorates cardiac dysfunction.大鼠心肌梗死后中期因子基因转移可防止重塑并改善心功能障碍。
Cardiovasc Res. 2010 Apr 1;86(1):113-21. doi: 10.1093/cvr/cvp386. Epub 2009 Dec 7.

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Control of the post-infarct immune microenvironment through biotherapeutic and biomaterial-based approaches.
通过生物治疗和基于生物材料的方法来控制梗死后的免疫微环境。
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Development and Long-Term Follow-Up of an Experimental Model of Myocardial Infarction in Rabbits.兔心肌梗死实验模型的建立与长期随访
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Message in a Bottle: Upgrading Cardiac Repair into Rejuvenation.瓶中信:将心脏修复升级为心脏再生。
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Translational Models of Arrhythmia Mechanisms and Susceptibility: Success and Challenges of Modeling Human Disease.心律失常机制与易感性的转化模型:人类疾病建模的成功与挑战
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J Cardiovasc Dev Dis. 2016 Oct 5;3(4):30. doi: 10.3390/jcdd3040030.
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Analysis of region specific gene expression patterns in the heart and systemic responses after experimental myocardial ischemia.实验性心肌缺血后心脏区域特异性基因表达模式及全身反应分析
Oncotarget. 2017 May 17;8(37):60809-60825. doi: 10.18632/oncotarget.17955. eCollection 2017 Sep 22.
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Outer Balloon Ligation Increases Success Rate of Ischemia-Reperfusion Injury Model in Mice.外置球囊结扎术提高小鼠缺血再灌注损伤模型的成功率。
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