Department of Medical Laboratory Diagnostics, Division of Clinical Chemistry, Wroclaw Medical University, Ul. Borowska 211A, 50-556 Wroclaw, Poland.
Department of Surgery, University of Saskatchewan, Saskatoon, SK, Canada.
Biomed Res Int. 2019 May 14;2019:9617087. doi: 10.1155/2019/9617087. eCollection 2019.
One of the greatest challenges facing the field of organ transplantation is the shortage of donor organs for transplantation. Renal transplantation increases quality of life and survival of patients suffering from end-stage renal disease. Although kidney transplantation has evolved greatly over the past few decades, a not insignificant amount of injury occurs to the kidney during recovery, preservation, and implantation and leads to the loss of function and loss of years of dialysis-free living for many patients. The use of kidneys from expanded criteria donors (ECD) and donation after circulatory determination of death (DCDD) has been adopted partly in response to the shortage of donor kidneys; however these kidneys are even more susceptible to ischemic injury. It has been shown that matrix metalloproteinases (MMPs) and reactive oxygen species (ROS) are involved in mechanisms of injury to the transplant kidney. There is also some evidence that inhibition of MMP activity and/or ROS production can protect the kidney from injury. We review possible pharmacological strategies for protection of kidney graft from injury during recovery, preservation, and implantation.
器官移植领域面临的最大挑战之一是供移植的器官短缺。肾移植可以提高终末期肾病患者的生活质量和生存率。尽管在过去几十年中,肾移植技术有了很大的发展,但在恢复、保存和植入过程中,肾脏仍会受到相当程度的损伤,导致许多患者的肾功能丧失,失去多年的无透析生活。为了应对供肾短缺的问题,人们已经部分采用了扩展标准供体(ECD)和循环死亡后捐献(DCDD)的肾脏;然而,这些肾脏更容易受到缺血性损伤。有研究表明,基质金属蛋白酶(MMPs)和活性氧(ROS)参与了移植肾损伤的机制。也有一些证据表明,抑制 MMP 活性和/或 ROS 生成可以保护肾脏免受损伤。我们回顾了在恢复、保存和植入过程中保护移植物免受损伤的可能的药物治疗策略。