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首页> 外文期刊>Transplantation Proceedings >Ischemia/reperfusion injury in kidney transplantation: mechanisms and prevention.
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Ischemia/reperfusion injury in kidney transplantation: mechanisms and prevention.

机译:肾脏移植中的缺血/再灌注损伤:机理和预防。

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Ischemia has been an inevitable event accompanying kidney transplantation. Ischemic changes start with brain death, which is associated with severe hemodynamic disturbances: increasing intracranial pressure results in bradycardia and decreased cardiac output; the Cushing reflex causes tachycardia and increased blood pressure; and after a short period of stabilization, systemic vascular resistance declines with hypotension leading to cardiac arrest. Free radical-mediated injury releases proinflammatory cytokines and activates innate immunity. It has been suggested that all of these changes-the early innate response and the ischemic tissue damage-play roles in the development of adaptive responses, which in turn may lead to an acute font of kidney rejection. Hypothermic kidney storage of various durations before transplantation add to ischemic tissue damage. The final stage of ischemic injury occurs during reperfusion. Reperfusion injury, the effector phase of ischemic injury, develops hours or days after the initial insult. Repair and regeneration processes occur together with cellular apoptosis, autophagy, and necrosis; the fate of the organ depends on whether cell death or regeneration prevails. The whole process has been described as the ischemia-reperfusion (I-R) injury. It has a profound influence on not only the early but also the late function of a transplanted kidney. Prevention of I-R injury should be started before organ recovery by donor pretreatment. The organ shortage has become one of the most important factors limiting extension of deceased donor kidney transplantation worldwide. It has caused increasing use of suboptimal deceased donors (high risk, extended criteria [ECD], marginal donors) and uncontrolled non-heart-beating (NHBD) donors. Kidneys from such donors are exposed to much greater ischemic damage before recovery and show reduced chances for proper early as well as long-term function. Storage of kidneys, especially those recovered from ECD (or NHBD) donors, should use machine perfusion.
机译:缺血是伴随肾脏移植的必然事件。缺血性改变始于脑死亡,这与严重的血液动力学障碍有关:颅内压升高导致心动过缓和心输出量降低;库欣反射会导致心动过速和血压升高;在短暂的稳定之后,系统性血管阻力会随着低血压而下降,从而导致心脏骤停。自由基介导的损伤释放促炎细胞因子并激活先天免疫。已经提出所有这些变化-早期先天反应和局部缺血性组织损伤在适应性反应的发展中发挥作用,这反过来可能导致急性肾排斥。移植前不同时间的低温肾存储增加了缺血性组织损伤。缺血性损伤的最后阶段发生在再灌注期间。再灌注损伤是缺血性损伤的效应期,在最初的侮辱后数小时或数天发展。修复和再生过程与细胞凋亡,自噬和坏死一起发生。器官的命运取决于细胞死亡或再生是否普遍。整个过程被描述为缺血再灌注(I-R)损伤。它不仅对移植肾的早期功能而且对晚期功能都有深远的影响。在通过供体预​​处理恢复器官之前,应开始预防I-R损伤。器官短缺已经成为限制已故的供体肾脏移植在世界范围内扩展的最重要因素之一。它导致越来越多的人使用了次优的死者(高风险,扩展标准[ECD],边缘性捐助者)和不受控制的非心跳(NHBD)捐助者。来自此类供体的肾脏在恢复之前会遭受更大的缺血损伤,并且早期和长期功能的机率降低。肾脏的存储,尤其是从ECD(或NHBD)供体中回收的肾脏,应使用机器灌注。

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