Tediashvili Grigol, Wang Dong, Reichenspurner Hermann, Deuse Tobias, Schrepfer Sonja
Transplant and Stem Cell Immunobiology Lab, University Heart Center; Department of Surgery, Transplant and Stem Cell Immunobiology Lab, University of California San Francisco (UCSF); Cardiovascular Research Center (CVRC) and DZHK German Center for Cardiovascular Research.
Transplant and Stem Cell Immunobiology Lab, University Heart Center; Department of Surgery, Transplant and Stem Cell Immunobiology Lab, University of California San Francisco (UCSF); Cardiovascular Research Center (CVRC) and DZHK German Center for Cardiovascular Research; Cardiovascular Surgery, University Heart Center.
J Vis Exp. 2018 Feb 7(132):56477. doi: 10.3791/56477.
The use of animal models is essential for a better understanding of MH, one major cause for arterial stenosis.In this article, we demonstrate a murine balloon denudation model, which is comparable with established vessel injury models in large animals. The aorta denudation model with balloon catheters mimics the clinical setting and leads to comparable pathobiological and physiological changes. Briefly, after performing a horizontal incision in the aorta abdominalis, a balloon catheter will be inserted into the vessel, inflated, and introduced retrogradely. Inflation of the balloon will lead to intima injury and overdistension of the vessel. After removing the catheter, the aortic incision will be closed with single stiches. The model shown in this article is reproducible, easy to perform, and can be established quickly and reliably. It is especially suitable for evaluating expensive experimental therapeutic agents, which can be applied in an economical fashion. By using different knockout-mouse strains, the impact of different genes on MH development can be assessed.
使用动物模型对于更好地理解动脉狭窄的主要原因之一——内膜增生(MH)至关重要。在本文中,我们展示了一种小鼠球囊剥脱模型,该模型与大型动物中已建立的血管损伤模型相当。用球囊导管进行的主动脉剥脱模型模拟了临床情况,并导致类似的病理生物学和生理学变化。简要地说,在腹主动脉进行水平切口后,将球囊导管插入血管,充气并逆行引入。球囊充气会导致内膜损伤和血管过度扩张。取出导管后,主动脉切口用单针缝合关闭。本文所示的模型具有可重复性、易于操作,并且可以快速可靠地建立。它特别适合评估昂贵的实验治疗药物,这些药物可以以经济的方式应用。通过使用不同的基因敲除小鼠品系,可以评估不同基因对内膜增生发展的影响。