The use of in situ perfusion of the rat mesentery as a model to investigate vascular injury directly induced by drugs.

A D Knapton, J Zhang, F D Sistare, J P Hanig
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引用次数: 8

Abstract

Exposure of the vasculature to vasodilators, pharmaceuticals and industrial chemicals may lead to injury of the blood vessel wall in animals. Vascular injury may begin with changes in the permeability of vascular endothelial cell and vessels, resulting in possible hemorrhage and edema leading subsequently to immune cell infiltration. The present study was undertaken to determine if the direct exposure of the Sprague Dawley rat mesenteric vasculature through the perfusion of aminophylline, fenoldopam, compound 48/80, histamine or serotonin has any such effects on the blood vessels, and if the two vital dyes Monastral blue B and Evans blue can be used to enhance the visualization of the vascular damage. Microscopic visualization was enhanced by the use of dyes and a variety of alterations of the perfused mesenteric vessels were detected, including varying degrees of mast cell degranulation, microvascular vasodilatation and increased vascular permeability. Macroscopic evidence of vascular damage was minimal. This study demonstrates that in situ perfusion of the rat mesentery is a simple and useful method to eliminate the influence of a variety of physiologic influences or homeostatic responses and can be used to further investigate drug-induced vascular damage.

以大鼠肠系膜原位灌注为模型,研究药物直接致血管损伤。
血管扩张剂、药物和工业化学品可能导致动物血管壁损伤。血管损伤可能始于血管内皮细胞和血管通透性的改变,可能导致出血和水肿,随后导致免疫细胞浸润。本研究旨在确定是否直接暴露于大鼠肠系膜血管,通过灌注氨茶碱、非诺多巴、化合物48/80、组胺或血清素对血管有任何此类影响,以及是否可以使用两种重要染料Monastral蓝B和Evans蓝来增强血管损伤的可视化。使用染料增强了显微镜下的可视化,并检测到灌注的肠系膜血管的各种变化,包括不同程度的肥大细胞脱颗粒,微血管血管扩张和血管通透性增加。血管损伤的肉眼证据极少。本研究表明,大鼠肠系膜原位灌注是消除多种生理影响或稳态反应影响的一种简单有效的方法,可用于进一步研究药物性血管损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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