Suppr超能文献

通过靶向含3个吡啉结构域的核苷酸结合寡聚化结构域样受体家族炎性小体确定WT161为治疗结肠炎的有效药物。

Identification of WT161 as a Potent Agent for the Treatment of Colitis by Targeting the Nucleotide-Binding Domain-Like Receptor Family Pyrin Domain Containing 3 Inflammasome.

作者信息

Long Xiuyan, Yu Xiaoyu, Gong Pan, Wang Xiaoyan, Tian Li

机构信息

Department of Gastroenterology, The Third Xiangya Hospital, Central South University, Changsha, China.

出版信息

Front Pharmacol. 2022 Mar 7;13:780179. doi: 10.3389/fphar.2022.780179. eCollection 2022.

Abstract

Inflammatory bowel diseases (IBD), including Crohn's disease and ulcerative colitis (UC), are chronic and recurrent intestinal inflammatory disorders. Numerous studies have revealed that the nucleotide-binding domain-like receptor family pyrin domain containing 3 (NLRP3) inflammasome plays a pivotal role in the pathogenesis of IBD, and inhibition of the NLRP3 inflammasome alleviates colitis in experimental animals. Our previous study showed that C646, an inhibitor of histone acetyltransferase p300, has a protective role in dextran sulfate sodium (DSS)-induced colitis by targeting the NLRP3 inflammasome, making us further study the inhibitors of histone deacetylases (HDACs) in the treatment of colitis. In this study, we have shown that WT161, an inhibitor of HDAC6, exerts a protective role in a colitis model, blocks NLRP3 inflammasome activation, disrupts ASC speck formation, and decreases the expression of NLRP3. This study uncovers a new inhibitor of the NLRP3 inflammasome and suggests its potential application in the treatment of active IBD.

摘要

炎症性肠病(IBD),包括克罗恩病和溃疡性结肠炎(UC),是慢性复发性肠道炎症性疾病。大量研究表明,含NOD样受体蛋白3(NLRP3)的炎性小体在IBD发病机制中起关键作用,抑制NLRP3炎性小体可减轻实验动物的结肠炎。我们之前的研究表明,组蛋白乙酰转移酶p300抑制剂C646通过靶向NLRP3炎性小体对葡聚糖硫酸钠(DSS)诱导的结肠炎具有保护作用,这促使我们进一步研究组蛋白去乙酰化酶(HDAC)抑制剂在结肠炎治疗中的作用。在本研究中,我们发现HDAC6抑制剂WT161在结肠炎模型中发挥保护作用,阻断NLRP3炎性小体激活,破坏凋亡相关斑点样蛋白(ASC)斑点形成,并降低NLRP3表达。本研究发现了一种新的NLRP3炎性小体抑制剂,并提示其在活动性IBD治疗中的潜在应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b72/8940270/c1c3dc834bc6/fphar-13-780179-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验