Stockmans F, Stassen J M, Vermylen J, Hoylaerts M F, Nyström A
Center for Molecular and Vascular Biology, University of Leuven, Belgium.
Ann Plast Surg. 1997 Jan;38(1):56-62. doi: 10.1097/00000637-199701000-00011.
Numerous clinically relevant animal models exist for thrombosis studies. Few of these are suitable for both arteries and veins. In this investigation, an established venous thrombosis model was adapted through minimal technical adjustments to allow also the study of arterial thrombosis. A standardized subintimal crush injury was performed to carotid arteries or femoral veins of hamsters. Thrombus volumes were then quantified by direct morphometric measurements from serial microscopic sections or by on-line image analysis of light intensity changes from transilluminated vessels. The platelet-rich mural thrombus, which was established within minutes of the trauma, disintegrated during the observation period. The life cycle of the thrombus was different in arteries and veins, but significant linear correlation (p < 0.01) was found in both types of vessel between thrombus volumes measured by the two techniques. The model can consequently be used for comparative in vivo thrombosis studies in small (approximately 1-mm) arteries and veins.
有许多用于血栓形成研究的临床相关动物模型。其中很少有适用于动脉和静脉的。在本研究中,通过最小的技术调整对已建立的静脉血栓形成模型进行了改进,以使其也能用于动脉血栓形成的研究。对仓鼠的颈动脉或股静脉进行标准化的内膜下挤压损伤。然后通过对连续显微镜切片进行直接形态测量或通过对透照血管的光强度变化进行在线图像分析来定量血栓体积。富含血小板的壁血栓在创伤后几分钟内形成,并在观察期内解体。血栓在动脉和静脉中的生命周期不同,但两种血管中通过两种技术测量的血栓体积之间均存在显著的线性相关性(p < 0.01)。因此,该模型可用于小型(约1毫米)动脉和静脉的体内血栓形成比较研究。