Dept. of Pharmacology and Toxicology, Univ. of Arkansas for Medical Sciences, 4301 W. Markham, no. 638, Little Rock, AR 72205.
Am J Physiol Renal Physiol. 2013 Oct 1;305(7):F1022-30. doi: 10.1152/ajprenal.00532.2012. Epub 2013 Jul 3.
Cold storage of kidneys before transplantation is problematic because of the limited survival time of the allografts. In this study, zinc-N-acetylcysteine (ZnNAC) was shown to be a potent endonuclease inhibitor and antioxidant, and it was tested as a potential additive to a cold storage solution for kidney preservation. Exposure of normal rat kidney NRK-52E cells to ZnNAC resulted in zinc delivery to the cells as determined by TFL-Zn fluorophore and partial protection of the cells against injury by cold storage in University of Wisconsin solution (UWS) as measured by propidium iodide assay. Ex vivo, rat kidneys demonstrated time- and temperature-dependent DNA fragmentation as assessed by TUNEL assay, indicating irreversible cell death. DNA fragmentation was faster in the medulla than in the cortex, and tubules were affected more than glomeruli. Perfusion of rat kidneys with cold ZnNAC solution in UWS significantly inhibited cell death both in the cortex and medulla at concentrations of 0.3-30 mM compared with UWS alone, with a maximum effect at 1-10 mM ZnNAC. Cold storage of the kidney significantly increased quantities of cleaved caspase-3 and endonuclease G (EndoG) in the tissue, which were abolished by 10 mM ZnNAC, indicating its ability to suppress both caspase-dependent and -independent cell death. Therefore, supplementation of UWS with ZnNAC can decrease DNA fragmentation and protect kidney allografts from cell death due to cold storage.
冷储存肾脏在移植前存在问题,因为同种异体移植物的存活时间有限。在这项研究中,锌-N-乙酰半胱氨酸(ZnNAC)被证明是一种有效的核酸内切酶抑制剂和抗氧化剂,它被测试为一种潜在的添加剂,用于保存肾脏的冷储存溶液。正常大鼠肾 NRK-52E 细胞暴露于 ZnNAC 导致细胞内锌的递送,如 TFL-Zn 荧光探针所测定的;冷储存于威斯康星大学溶液(UWS)中对细胞的部分保护作用,如碘化丙啶测定所测定的。在体,大鼠肾脏通过 TUNEL 测定法显示出时间和温度依赖性的 DNA 片段化,表明不可逆的细胞死亡。在髓质中,DNA 片段化比皮质中更快,且小管比肾小球更易受影响。与 UWS 单独相比,用冷 ZnNAC 溶液在 UWS 中灌注大鼠肾脏可显著抑制皮质和髓质中的细胞死亡,在 0.3-30 mM 的浓度下,以 1-10 mM ZnNAC 的浓度作用最大。冷储存显著增加了组织中裂解的半胱天冬酶-3 和核酸内切酶 G(EndoG)的数量,这被 10 mM ZnNAC 消除,表明其抑制 caspase 依赖性和非依赖性细胞死亡的能力。因此,用 ZnNAC 补充 UWS 可以减少 DNA 片段化,并保护肾脏同种异体移植物免受冷储存引起的细胞死亡。