Okada Y, Marchevsky A M, Zuo X J, Pass J A, Kass R M, Matloff J M, Jordan S C
Department of Cardiothoracic Surgery, The Cedars-Sinai Medical Center Burns and Allen Research Institute, UCLA School of Medicine, Los Angeles, California 90048, USA.
Transplantation. 1997 Sep 27;64(6):801-6. doi: 10.1097/00007890-199709270-00002.
Platelets are known to play an important role in the pathogenesis of adult respiratory distress syndrome as well as preservation-reperfusion injury of liver allografts. However, the role of platelets in pulmonary preservation-reperfusion injury is unknown. In this study, we examined whether the extent of platelet accumulation in the preserved and subsequently reperfused lungs correlated with the degree of preservation-reperfusion injury in a rat lung isotransplant model.
Heart-lung blocks from donor rats were flushed with and preserved in modified Euro-Collins solution at 4 degrees C for 0 hr (n=5), 6 hr (n=6), and 24 hr (n=6). The left lung was divided from the heart-lung block, transplanted into the recipient rat, and reperfused for 1 hr. Lung injury was evaluated by the left-to-right pulmonary blood flow ratio, the weight gain of the isograft, and the scores for histological categories of lung injury (intra-alveolar edema, intra-alveolar hemorrhage, and capillary congestion). Small portions of the lung isograft were excised and stained with an antibody specific for rat platelets. A scoring system was developed to semiquantitate the intensity of antibody staining in isografts.
Lung isografts were injured and platelets accumulated in the capillaries in proportion to the length of preservation endured before transplantation. The extent of platelet accumulation evaluated by our morphological scoring system correlated significantly with the degree of lung injury assessed by the blood flow ratio (P<0.001), the weight gain (P<0.001), and the histological scores for intra-alveolar hemorrhage (P<0.05) and for capillary congestion (P<0.001).
The results of this study suggest that platelet accumulation is a potential factor responsible for preservation-reperfusion injury of lung isografts in the rat.
已知血小板在成人呼吸窘迫综合征的发病机制以及肝移植保存-再灌注损伤中起重要作用。然而,血小板在肺保存-再灌注损伤中的作用尚不清楚。在本研究中,我们在大鼠肺同基因移植模型中检测了保存及随后再灌注的肺中血小板聚集程度是否与保存-再灌注损伤程度相关。
将供体大鼠的心-肺块用改良的Euro-Collins溶液冲洗,并在4℃保存0小时(n = 5)、6小时(n = 6)和24小时(n = 6)。将左肺从心-肺块上分离,移植到受体大鼠体内,并再灌注1小时。通过左右肺血流比、同种异体移植肺的重量增加以及肺损伤组织学分类(肺泡内水肿、肺泡内出血和毛细血管充血)评分来评估肺损伤。切除一小部分肺同种异体移植组织,并用针对大鼠血小板的特异性抗体进行染色。开发了一种评分系统来半定量同种异体移植组织中抗体染色的强度。
肺同种异体移植组织受到损伤,并且血小板在毛细血管中的聚集与移植前保存的时间长度成正比。通过我们的形态学评分系统评估的血小板聚集程度与通过血流比(P < 0.001)、重量增加(P < 0.001)以及肺泡内出血(P < 0.05)和毛细血管充血(P < 0.001)的组织学评分评估的肺损伤程度显著相关。
本研究结果表明,血小板聚集是大鼠肺同种异体移植保存-再灌注损伤的一个潜在因素。