Zens Tiffany J, Danobeitia Juan S, Chlebeck Peter J, Zitur Laura J, Odorico Scott, Brunner Kevin, Coonen Jennifer, Capuano Saverio, D'Alessandro Anthony M, Matkowskyj Kristina, Zhong Weixiong, Torrealba Jose, Fernandez Luis
University of Wisconsin Department of Surgery, Division of Transplantation, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, United States of America.
Wisconsin Primate Research Center, University of Wisconsin, Madison, Wisconsin, United States of America.
PLoS One. 2017 Sep 19;12(9):e0182552. doi: 10.1371/journal.pone.0182552. eCollection 2017.
The development of a translatable brain death animal model has significant potential to advance not only transplant research, but also the understanding of the pathophysiologic changes that occur in brain death and severe traumatic brain injury. The aim of this paper is to describe a rhesus macaque model of brain death designed to simulate the average time and medical management described in the human literature.
Following approval by the Institutional Animal Care and Use Committee, a brain death model was developed. Non-human primates were monitored and maintained for 20 hours after brain death induction. Vasoactive agents and fluid boluses were administered to maintain hemodynamic stability. Endocrine derangements, particularly diabetes insipidus, were aggressively managed.
A total of 9 rhesus macaque animals were included in the study. The expected hemodynamic instability of brain death in a rostral to caudal fashion was documented in terms of blood pressure and heart rate changes. During the maintenance phase of brain death, the animal's temperature and hemodynamics were maintained with goals of mean arterial pressure greater than 60mmHg and heart rate within 20 beats per minute of baseline. Resuscitation protocols are described so that future investigators may reproduce this model.
We have developed a reproducible large animal primate model of brain death which simulates clinical scenarios and treatment. Our model offers the opportunity for researchers to have translational model to test the efficacy of therapeutic strategies prior to human clinical trials.
可转化的脑死亡动物模型的开发不仅在推进移植研究方面具有巨大潜力,而且在理解脑死亡和严重创伤性脑损伤中发生的病理生理变化方面也具有重要意义。本文旨在描述一种恒河猴脑死亡模型,该模型旨在模拟人类文献中描述的平均时间和医疗管理。
在获得机构动物护理和使用委员会的批准后,开发了一种脑死亡模型。对非人灵长类动物在诱导脑死亡后进行20小时的监测和维持。给予血管活性药物和液体冲击以维持血流动力学稳定。积极处理内分泌紊乱,特别是尿崩症。
该研究共纳入9只恒河猴动物。记录了脑死亡从头部到尾部预期的血流动力学不稳定情况,包括血压和心率变化。在脑死亡维持阶段,通过将平均动脉压维持在大于60mmHg且心率维持在基线值每分钟20次心跳以内的目标来维持动物的体温和血流动力学。描述了复苏方案,以便未来的研究人员能够复制该模型。
我们开发了一种可重复的大型动物灵长类脑死亡模型,该模型模拟了临床情况和治疗方法。我们的模型为研究人员提供了一个转化模型,以便在人类临床试验之前测试治疗策略的疗效。