...
首页> 外文期刊>Journal of proteomics >Proteomic analysis reveals the protective effects of emodin on severe acute pancreatitis induced lung injury by inhibiting neutrophil proteases activity
【24h】

Proteomic analysis reveals the protective effects of emodin on severe acute pancreatitis induced lung injury by inhibiting neutrophil proteases activity

机译:蛋白质组学分析揭示了大黄素对严重急性胰腺炎诱导肺损伤的保护作用通过抑制中性粒细胞蛋白酶活性

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Acute lung injury (ALI) is the most common remote organ complication induced by severe acute pancreatitis (SAP). Almost 60-70% SAP-induced deaths are caused by ALI. Efficient clinical therapeutic strategy for SAP-induced ALI is still lacking. In this study, we demonstrate that Emodin (EMO) can significantly alleviate SAP-induced ALI. We investigate the therapeutic mechanisms of EMO by proteomic analysis, which indicates that EMO protects lung tissue against SAP-ALI by negative regulation of endopeptidase activity and inhibition of collagen-containing extracellular matrix degradation. Protein-protein interaction analysis showed Lamc2, Serpinal and Serpinbl play important roles in the above pathways. This study elucidates the possible mechanism and suggests the candidacy of EMO in the clinical treatment of SAP-ALI.
机译:急性肺损伤(ALI)是严重急性胰腺炎(SAP)诱导的最常见的偏远器官并发症。 近60-70%的SAP诱导的死亡是由ALI引起的。 缺乏高效的SAP诱发ALI的临床治疗策略。 在这项研究中,我们证明了大黄素(EMO)可以显着减轻SAP诱导的ALI。 我们通过蛋白质组学分析研究了EMO的治疗机制,表明EMO通过内肽酶活性的负调节和含胶原蛋白的细胞外基质降解的抑制来保护肺组织免受SAP-ALI的影响。 蛋白质 - 蛋白质相互作用分析显示LAMC2,Serpinal和SerpinBL在上述途径中起重要作用。 本研究阐明了可能的机制,并提出了EMO在SAP-ALI的临床治疗中的候选性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号