Department of Surgery, University Hospital Maastricht and Nutrition and Toxicology Research Institute, Maastricht University, Maastricht, The Netherlands.
J Surg Res. 2011 Apr;166(2):222-6. doi: 10.1016/j.jss.2009.09.046. Epub 2009 Oct 22.
This report describes a human in vivo ischemia reperfusion (IR) model of the small intestine. Animal models of intestinal IR are indispensable for our understanding of sequelae of IR induced organ damage. However, a functional experimental IR model of the human small intestine, allowing for translational research, can be considered critical for our pathophysiologic understanding of intestinal IR in man.
Patients with a healthy gut undergoing abdominal surgery with a Roux-Y or similar reconstruction were included, creating the opportunity to study IR of an isolated jejunal segment in a harmless model.
Ischemia was induced by nontraumatic vascular clamping followed by reperfusion. This model can be adapted using variable ischemia and reperfusion times. Similarly, tissue and plasma can be collected at any given time point during ischemia until end of reperfusion, only determined by progress of the original, intended surgical procedure.
A unique and harmless human IR model of the jejunum was created, which enables the study of acute damage to the epithelial lining and its subsequent repair mechanisms.
本报告描述了一种人体小肠的局部缺血再灌注(IR)模型。动物的肠道 IR 模型对于我们理解 IR 诱导的器官损伤的后遗症是不可或缺的。然而,一个能够进行转化研究的人类小肠功能实验性 IR 模型,可以被认为对于我们在人类中理解肠道 IR 的病理生理机制至关重要。
纳入了接受腹部手术且行 Roux-Y 或类似重建的健康肠道患者,为研究孤立空肠段的 IR 提供了机会。
通过非创伤性血管夹闭诱导缺血,然后再灌注。可以根据不同的缺血和再灌注时间来调整该模型。同样,在整个再灌注过程中,可以在任意给定的缺血时间点收集组织和血浆,仅取决于最初预期手术的进展。
创建了一种独特且无害的人类空肠 IR 模型,该模型可用于研究上皮衬里的急性损伤及其随后的修复机制。