Section of Transplantation Surgery, Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.
Section of Clinical Immunology, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Transplantation. 2019 Feb;103(2):420-427. doi: 10.1097/TP.0000000000002469.
Previously, we have been able to demonstrate the possibility of coating the inner surface of the renal arteries in porcine kidneys with a heparin conjugate during hypothermic machine perfusion (HMP). The purpose of this study was to assess the efficacy of this treatment in reducing early ischemia-reperfusion injury.
Brain death was induced in male landrace pigs by stepwise volume expansion of an epidural balloon catheter until negative cerebral perfusion pressure (CPP) was obtained. Both kidneys (matched pairs; n = 6 + 6) were preserved for 20 hours by HMP during which 50 mg heparin conjugate was added to one of the HMP systems (treated group). A customized ex vivo normothermic oxygenated perfusion (NP) system with added exogenous creatinine was used to evaluate early kidney function. Blood, urine and histological samples were collected during the subsequent 3 hours of NP.
Kidney weight was lower at the end of NP (P = 0.017) in the treated group compared with control kidneys. The rate of decline in creatinine level was faster (P = 0.024), total urinary volume was higher (P = 0.031), and the level of urine neutrophil gelatinase-associated lipocalin (NGAL) was lower (P = 0.031) in the treated group. Histologically, less tubular changes were seen (P = 0.046). During NP intrarenal resistance remained lower (P < 0.0001) in the treated group.
Perfusion of porcine kidneys with heparin conjugate during HMP reduces preservation injury and improves organ function shortly after reperfusion. No increased risk of bleeding was seen in this setup. This protective strategy may potentially improve the quality of transplanted kidneys in the clinical setting.
此前,我们已经能够在低温机器灌注(HMP)期间将肝素缀合物涂覆到猪肾的动脉内表面。本研究的目的是评估该治疗方法在减少早期缺血再灌注损伤方面的效果。
通过逐步扩张硬膜外球囊导管使雄性长白猪发生脑死亡,直到获得负的脑灌注压(CPP)。通过 HMP 保存 20 小时的两个肾脏(匹配对;n = 6 + 6),其中一个 HMP 系统中添加了 50mg 肝素缀合物(治疗组)。使用定制的体外常温充氧灌注(NP)系统,并添加外源性肌酐来评估早期肾功能。在随后的 3 小时 NP 期间收集血液、尿液和组织学样本。
与对照组肾脏相比,NP 结束时治疗组肾脏的重量较低(P = 0.017)。肌酐水平下降速度更快(P = 0.024),总尿量较高(P = 0.031),尿液中性粒细胞明胶酶相关脂质运载蛋白(NGAL)水平较低(P = 0.031)。组织学上,肾小管变化较少(P = 0.046)。在 NP 期间,治疗组肾内阻力保持较低(P < 0.0001)。
在 HMP 期间用肝素缀合物灌注猪肾可减少保存损伤,并在再灌注后不久改善器官功能。在这种设置中未发现出血风险增加。这种保护策略可能会在临床环境中提高移植肾脏的质量。