华大补充 AP39 可提高静态冷藏后的肝脏活力

S Taggart McLean, Saige Holkup, Alexandra Tchir, Mohammadreza Mojoudi, Madeeha Hassan, Christopher Taveras, S Ozgur Ozge, F Markmann James, Heidi Yeh, Korkut Uygun, Alban Longchamp
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引用次数: 0

摘要

供体肝脏在 4°C 的静态冷藏不能完全阻止新陈代谢,最终导致 ATP 水平下降、氧化应激、细胞死亡和器官衰竭。硫化氢(H 2 S)是一种内源性气体,以前曾被证实能减轻氧化应激、减少 ATP 消耗并防止缺血和再灌注损伤。由于 H 2 S 的释放曲线很快,因此很难施用,高浓度时会导致细胞死亡。AP39 是一种靶向线粒体的缓释 H 2 S 供体,已被证明能减轻心脏和肾脏的缺血再灌注损伤。因此,我们研究了在3天静态冷藏期间添加AP39是否能提高肝脏移植的存活率。储存结束后,肝脏接受了六小时的无细胞常温机器灌注,这是一种移植模型。在模拟移植过程中,用 AP39 储存的肝脏表现出抵抗力下降、细胞损伤(谷丙转氨酶和谷草转氨酶)减少以及细胞凋亡减少。此外,添加 AP39 还能改善胆汁分泌和葡萄糖以及能量充注。这些结果表明,补充 AP39 可提高肝脏在静态冷藏期间的存活率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
UW Supplementation with AP39 Improves Liver Viability Following Static Cold Storage.

Static cold storage of donor livers at 4°C incompletely arrests metabolism, ultimately leading to decreases in ATP levels, oxidative stress, cell death, and organ failure. Hydrogen Sulfide (H2S) is an endogenously produced gas, previously demonstrated to reduce oxidative stress, reduce ATP depletion, and protect from ischemia and reperfusion injury. H2S is difficult to administer due to its rapid release curve, resulting in cellular death at high concentrations. AP39, a mitochondrially targeted, slow-release H2S donor, has been shown to reduce ischemia-reperfusion injury in hearts and kidneys. Thus, we investigated whether the addition of AP39 during 3-day static cold storage can improve liver graft viability. At the end of storage, livers underwent six hours of acellular normothermic machine perfusion, a model of transplantation. During simulated transplantation, livers stored with AP39 showed reduced resistance, reduced cellular damage (ALT and AST), and reduced apoptosis. Additionally, bile production and glucose, as well as energy charge were improved by the addition of AP39. These results indicate that AP39 supplementation improves liver viability during static cold storage.

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