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一种用于研究血管通透性增加的失血性休克大鼠模型。

A Rat Model of Hemorrhagic Shock for Studying Vascular Hyperpermeability.

作者信息

Esiobu Prince, Childs Ed W

机构信息

Department of Surgery, Morehouse School of Medicine, Atlanta, GA, USA.

出版信息

Methods Mol Biol. 2018;1717:53-60. doi: 10.1007/978-1-4939-7526-6_5.

Abstract

Vascular hyperpermeability is one of the known detrimental effects of hemorrhagic shock, which we continually try to understand, minimize, and reverse. Here, we describe induction of hemorrhagic shock in a rat and studying of its effects on vascular permeability, using intravital microscopy. In this protocol, hemorrhagic shock will be induced by withdrawing blood to reduce the mean arterial pressure (MAP) to 40 mmHg for 60 min followed by resuscitation for 60 min. To study the changes in vascular permeability following hemorrhagic shock, the rats will be given FITC-albumin, a fluorescent tracer, intravenously. Following this, the FITC-albumin flux across the vessel will be measured in mesenteric postcapillary venules by determining fluorescent intensity intravascularly and extravascularly under intravital microscopy.

摘要

血管通透性增加是失血性休克已知的有害影响之一,我们一直在努力了解、尽量减少并逆转这种影响。在此,我们描述了在大鼠中诱导失血性休克并使用活体显微镜研究其对血管通透性的影响。在本方案中,通过抽血将平均动脉压(MAP)降至40 mmHg持续60分钟,随后复苏60分钟来诱导失血性休克。为了研究失血性休克后血管通透性的变化,将向大鼠静脉注射荧光示踪剂异硫氰酸荧光素标记的白蛋白(FITC-白蛋白)。在此之后,通过在活体显微镜下测定血管内和血管外的荧光强度,测量肠系膜毛细血管后微静脉中FITC-白蛋白跨血管的通量。

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