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心肌缺血和梗死实验模型指南。

Guidelines for experimental models of myocardial ischemia and infarction.

机构信息

Mississippi Center for Heart Research, Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi.

Research Service, G. V. (Sonny) Montgomery Veterans Affairs Medical Center , Jackson, Mississippi.

出版信息

Am J Physiol Heart Circ Physiol. 2018 Apr 1;314(4):H812-H838. doi: 10.1152/ajpheart.00335.2017. Epub 2018 Jan 12.


DOI:10.1152/ajpheart.00335.2017
PMID:29351451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5966768/
Abstract

Myocardial infarction is a prevalent major cardiovascular event that arises from myocardial ischemia with or without reperfusion, and basic and translational research is needed to better understand its underlying mechanisms and consequences for cardiac structure and function. Ischemia underlies a broad range of clinical scenarios ranging from angina to hibernation to permanent occlusion, and while reperfusion is mandatory for salvage from ischemic injury, reperfusion also inflicts injury on its own. In this consensus statement, we present recommendations for animal models of myocardial ischemia and infarction. With increasing awareness of the need for rigor and reproducibility in designing and performing scientific research to ensure validation of results, the goal of this review is to provide best practice information regarding myocardial ischemia-reperfusion and infarction models. Listen to this article's corresponding podcast at ajpheart.podbean.com/e/guidelines-for-experimental-models-of-myocardial-ischemia-and-infarction/.

摘要

心肌梗死是一种常见的主要心血管事件,由心肌缺血伴或不伴再灌注引起,需要基础和转化研究来更好地了解其潜在机制及其对心脏结构和功能的影响。缺血是从心绞痛到冬眠到永久性闭塞等广泛临床情况的基础,尽管再灌注是从缺血损伤中抢救的必要条件,但再灌注本身也会造成损伤。在本共识声明中,我们提出了心肌缺血和梗死动物模型的建议。随着人们越来越意识到在设计和进行科学研究时需要严谨性和可重复性,以确保结果的验证,本综述的目的是提供关于心肌缺血-再灌注和梗死模型的最佳实践信息。请在 ajpheart.podbean.com/e/guidelines-for-experimental-models-of-myocardial-ischemia-and-infarction/ 收听本文的相应播客。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8267/5966768/2ccd1a453f60/zh40031824550001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8267/5966768/2ccd1a453f60/zh40031824550001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8267/5966768/2ccd1a453f60/zh40031824550001.jpg

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本文引用的文献

[1]
Guidelines for measuring cardiac physiology in mice.

Am J Physiol Heart Circ Physiol. 2018-1-5

[2]
STAT3 as a common signal of ischemic conditioning: a lesson on "rigor and reproducibility" in preclinical studies on cardioprotection.

Basic Res Cardiol. 2017-11-20

[3]
Heart functional and structural compendium of cardiosplenic and cardiorenal networks in acute and chronic heart failure pathology.

Am J Physiol Heart Circ Physiol. 2017-11-3

[4]
VEGF nanoparticles repair the heart after myocardial infarction.

Am J Physiol Heart Circ Physiol. 2017-11-3

[5]
Transient denervation of viable myocardium after myocardial infarction does not alter arrhythmia susceptibility.

Am J Physiol Heart Circ Physiol. 2017-11-3

[6]
Macrophage overexpression of matrix metalloproteinase-9 in aged mice improves diastolic physiology and cardiac wound healing after myocardial infarction.

Am J Physiol Heart Circ Physiol. 2017-10-13

[7]
Brief Myocardial Ischemia Produces Cardiac Troponin I Release and Focal Myocyte Apoptosis in the Absence of Pathological Infarction in Swine.

JACC Basic Transl Sci. 2017-4

[8]
Proteomics/phosphoproteomics of left ventricular biopsies from patients with surgical coronary revascularization and pigs with coronary occlusion/reperfusion: remote ischemic preconditioning.

Sci Rep. 2017-8-9

[9]
Impact of electrical defibrillation on infarct size and no-reflow in pigs subjected to myocardial ischemia-reperfusion without and with ischemic conditioning.

Am J Physiol Heart Circ Physiol. 2017-11-1

[10]
Intracoronary delivery of recombinant TIMP-3 after myocardial infarction: effects on myocardial remodeling and function.

Am J Physiol Heart Circ Physiol. 2017-10-1

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