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C57BL/6J小鼠的心肌梗死:一种可量化且高度可重复的实验模型。

Myocardial infarction in the C57BL/6J mouse: a quantifiable and highly reproducible experimental model.

作者信息

Salto-Tellez Manuel, Yung Lim Sing, El-Oakley Reida Menshawe, Tang Tiffany Pooi Ling, ALmsherqi Zakaria Ali Moh, Lim Sai-Kiang

机构信息

Department of Pathology, National University of Singapore, 5 Lower Kent Ridge Road 119074, Singapore.

出版信息

Cardiovasc Pathol. 2004 Mar-Apr;13(2):91-7. doi: 10.1016/S1054-8807(03)00129-7.

Abstract

INTRODUCTION

The laboratory mouse is a powerful tool in cardiovascular research. In this report, we describe a method for a reproducible mouse myocardial infarction model that would allow subsequent comparative and quantitative studies on molecular and pathophysiological variables.

METHODS

(A) The distribution of the major coronary arteries including the septal artery in the left ventricle of the C57BL/6J mice (n=20) was mapped by perfusion of latex dye or fluorescent beads through the aorta. (B) The territory of myocardial infarction after the ligation of the most proximal aspect of the left anterior descending (LAD) coronary artery was quantified. (C) The consistency in the histological changes parallel to the infarction at different time points was analyzed.

RESULTS

(A) The coronary artery tree of the mouse is different from human and, particularly, in regard to the blood supply of the septum. (B) Contrary to previous belief, the septal coronary artery in the mouse is variable in origin. (C) A constant ligation of the LAD immediately below the left auricular level ensures a statistically significant reproducible infarct size. (D) The ischemic changes can be monitored at a histological level in a way similar to what is described in the human.

CONCLUSION

We illustrate a method for maximal reproducibility of experimental acute myocardial infarction in the mouse model, due to a consistent loss of perfusion in the lower half of the left ventricle. This will allow the study of molecular and physiological variables in a controlled and quantifiable experimental model environment.

摘要

引言

实验室小鼠是心血管研究中的一种强大工具。在本报告中,我们描述了一种可重复的小鼠心肌梗死模型的方法,该方法将允许对分子和病理生理变量进行后续的比较和定量研究。

方法

(A)通过经主动脉灌注乳胶染料或荧光珠,绘制C57BL/6J小鼠(n = 20)左心室包括间隔动脉在内的主要冠状动脉的分布。(B)对结扎左冠状动脉前降支(LAD)最近端后心肌梗死的范围进行量化。(C)分析不同时间点与梗死平行的组织学变化的一致性。

结果

(A)小鼠的冠状动脉树与人类不同,特别是在间隔的血液供应方面。(B)与先前的观点相反,小鼠的间隔冠状动脉起源可变。(C)在左耳水平正下方持续结扎LAD可确保梗死面积具有统计学意义的可重复性。(D)缺血变化可以在组织学水平上以类似于人类描述的方式进行监测。

结论

我们阐述了一种在小鼠模型中实现实验性急性心肌梗死最大可重复性的方法,这是由于左心室下半部分灌注持续丧失所致。这将允许在可控且可量化的实验模型环境中研究分子和生理变量。

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