Tanaka Masashi, Mokhtari Golnaz K, Terry Raya D, Gunawan Feny, Balsam Leora B, Hoyt Grant, Lee Keun-Ho, Tsao Philip S, Robbins Robert C
Department of Cardiothoracic Surgery, Stanford University Medical Center, Stanford, California 94305, USA.
J Heart Lung Transplant. 2005 Nov;24(11):1906-14. doi: 10.1016/j.healun.2004.06.007. Epub 2005 Jul 27.
Prolonged cold ischemia is thought to exacerbate ischemia-reperfusion injury and graft coronary artery disease (GCAD). We investigated the effect of varying lengths of cold ischemia on inflammation and apoptosis during ischemia-reperfusion injury and correlated this with the degree of GCAD in rat cardiac allografts.
PVG rat (RT1c) hearts subjected to 30, 60, 90, 120, or 150 minutes of cold ischemia were heterotopically transplanted into ACI rats (RT1a). Grafts were procured after 4 hours of reperfusion and analyzed for superoxide generation, myeloperoxidase activity, tumor necrosis factor-alpha (TNF-alpha), interleukin-1beta (IL-1beta), and monocyte chemoattractant protein-1/chemokine (C-C motif) ligand 2 (MCP-1/CCL2) production, cardiomyocyte apoptosis, and caspase-2, -3, -8, -9 activities. Additional transplanted animals received cyclosporine A (7.5 mg/kg/day) for 10 days as chronic rejection models. Indices of GCAD were determined at 90 days.
A direct linear correlation was found between cold ischemic time, ischemia-reperfusion injury, and GCAD. Superoxide generation, myeloperoxidase activity, TNF-alpha, IL-1beta, MCP-1/CCL2 production, cardiomyocyte apoptosis, and caspase-2, -3, -8, and -9 activities increased with ischemic time, peaking at 120 minutes and plateauing at 150 minutes. GCAD, assessed by the percentage of luminal narrowing, the intima/media ratio, and the percentage of diseased vessels, worsened with increased ischemic time, peaking at 120 minutes and plateauing at 150 minutes. All tested variables in both the acute and chronic phases were significantly increased with 120-minute ischemia compared with 30-minute ischemia.
These data indicate that the degree of cardiomyocyte apoptosis and inflammatory response in cardiac allografts during ischemia-reperfusion injury depends on the duration of cold ischemia. More important, that prolonged cold ischemia correlates with increased GCAD.
长时间冷缺血被认为会加剧缺血再灌注损伤和移植冠状动脉疾病(GCAD)。我们研究了不同时长的冷缺血对缺血再灌注损伤期间炎症和细胞凋亡的影响,并将其与大鼠心脏同种异体移植中GCAD的程度相关联。
将经历30、60、90、120或150分钟冷缺血的PVG大鼠(RT1c)心脏异位移植到ACI大鼠(RT1a)体内。再灌注4小时后获取移植物,分析超氧化物生成、髓过氧化物酶活性、肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)以及单核细胞趋化蛋白-1/趋化因子(C-C基序)配体2(MCP-1/CCL2)的产生、心肌细胞凋亡以及半胱天冬酶-2、-3、-8、-9的活性。另外一些移植动物作为慢性排斥模型接受10天的环孢素A(7.5毫克/千克/天)治疗。在90天时测定GCAD指标。
发现冷缺血时间、缺血再灌注损伤和GCAD之间存在直接线性关系。超氧化物生成、髓过氧化物酶活性、TNF-α、IL-1β、MCP-1/CCL2的产生、心肌细胞凋亡以及半胱天冬酶-2、-3、-8和-9的活性随缺血时间增加,在120分钟时达到峰值,150分钟时趋于平稳。通过管腔狭窄百分比、内膜/中膜比值和病变血管百分比评估的GCAD随缺血时间延长而恶化,在120分钟时达到峰值,150分钟时趋于平稳。与30分钟缺血相比,120分钟缺血时急性和慢性期的所有测试变量均显著增加。
这些数据表明,缺血再灌注损伤期间心脏同种异体移植中心肌细胞凋亡程度和炎症反应取决于冷缺血持续时间。更重要的是,长时间冷缺血与GCAD增加相关。