Rosen E D, Raymond S, Zollman A, Noria F, Sandoval-Cooper M, Shulman A, Merz J L, Castellino F J
Department of Chemistry and Biochemistry, W. M. Keck Center for Transgene Research, University of Notre Dame, Notre Dame, Indiana, USA.
Am J Pathol. 2001 May;158(5):1613-22. doi: 10.1016/S0002-9440(10)64117-X.
A minimally invasive laser-induced injury model is described to study thrombus development in mice in vivo. The protocol involves focusing the beam of an argon-ion laser through a compound microscope on the vasculature of a mouse ear that is sufficiently thin such that blood flow can be visualized by intravital microscopy. Two distinct injury models have been established. The first involves direct laser illumination with a short, high-intensity pulse. In this case, thrombus formation is inhibited by the GPIIb/IIIa antagonist, G4120. However, the anticoagulants, hirulog, PPACK, and NapC2 have minimal effect. This indicates that thrombus development induced by this model mainly involves platelet interactions. The second model involves low-intensity laser illumination of mice injected with Rose Bengal dye to induce photochemical injury in the region of laser illumination. Thrombi generated by this latter procedure have a slower development and are inhibited by both anticoagulant and anti-platelet compounds.
描述了一种微创激光诱导损伤模型,用于在体内研究小鼠血栓形成。该方案包括通过复合显微镜将氩离子激光束聚焦在小鼠耳部血管上,小鼠耳部足够薄,使得通过活体显微镜可以观察到血流。已经建立了两种不同的损伤模型。第一种涉及用短时间高强度脉冲进行直接激光照射。在这种情况下,血栓形成受到糖蛋白IIb/IIIa拮抗剂G4120的抑制。然而,抗凝剂水蛭素、PPACK和NapC2的作用极小。这表明该模型诱导的血栓形成主要涉及血小板相互作用。第二种模型涉及对注射了孟加拉玫瑰红染料的小鼠进行低强度激光照射,以在激光照射区域诱导光化学损伤。后一种方法产生的血栓形成发展较慢,并且受到抗凝剂和抗血小板化合物的抑制。