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新型化合物PICCS可提高大鼠模型在冷藏期间的细胞活力,并减轻肺缺血再灌注损伤。

The novel compound PICCS improves cell viability during cold storage and reduces pulmonary ischemia-reperfusion injury in a rat model.

作者信息

Yokoyama Yuhei, Toyomoto Masayasu, Tanaka Nobuo, Tanaka Satona, Nishikawa Shigeto, Kayawake Hidenao, Morimura Yuki, Oda Hiromi, Yamauchi Momono, Yamamoto Makoto, Chen-Yoshikawa Toyofumi F, Hagiwara Masatoshi, Date Hiroshi

机构信息

Department of Thoracic Surgery, Kyoto University Hospital, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.

Department of Drug Discovery of Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

Sci Rep. 2025 Apr 30;15(1):15217. doi: 10.1038/s41598-025-99851-7.

Abstract

A simple method to achieve better organ preservation is the addition of compounds to the preservation solution, which effectively inhibits cold injury. We aimed to develop novel compounds for better lung graft preservation using TY52156 as a seed compound, which reportedly inhibits cold injury of vascular endothelial cells and exerts organ-protective effects in a rat heart transplant model. Eighteen compounds were newly synthesized and screened using an in vitro screening system for cold storage and rewarming. Among them, three of the synthesized compounds increased cell viability after 4 days of cold storage in both vascular endothelial and airway epithelial cells without cytotoxic effects. They were denoted as preventing inducible cell damage in cold stress (PICCS)-1, -2, and -3. PICCS-3 inhibited apoptotic signaling in airway epithelial cells after 6 h of cold storage. In a rat lung transplant ischemia-reperfusion injury (IRI) model, addition of PICCS-3 to the organ preservation solution attenuated IRI, as evidenced by improved physiological data of the lung graft, reduced lung edema, and extravasation of neutrophils. This study demonstrates the potential of a structure-based synthetic approach and an in vitro screening system using appropriate cell types to develop novel effective additives for organ preservation solutions.

摘要

一种实现更好器官保存的简单方法是在保存液中添加化合物,这能有效抑制冷损伤。我们旨在以TY52156作为起始化合物开发新型化合物,以实现更好的肺移植保存效果,据报道,TY52156可抑制血管内皮细胞的冷损伤,并在大鼠心脏移植模型中发挥器官保护作用。新合成了18种化合物,并使用体外冷藏和复温筛选系统进行筛选。其中,三种合成化合物在血管内皮细胞和气道上皮细胞冷藏4天后均提高了细胞活力,且无细胞毒性作用。它们被命名为冷应激诱导细胞损伤预防剂(PICCS)-1、-2和-3。冷藏6小时后,PICCS-3抑制了气道上皮细胞中的凋亡信号。在大鼠肺移植缺血再灌注损伤(IRI)模型中,向器官保存液中添加PICCS-3可减轻IRI,肺移植的生理数据改善、肺水肿减轻以及中性粒细胞渗出减少均证明了这一点。本研究证明了基于结构的合成方法和使用合适细胞类型的体外筛选系统在开发用于器官保存液的新型有效添加剂方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a97/12043901/55b92e69ee2c/41598_2025_99851_Fig1_HTML.jpg

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