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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.
Long, Xiuyan; Yu, Xiaoyu; Gong, Pan; Wang, Xiaoyan; Tian, Li.
Affiliation
  • Long X; Department of Gastroenterology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Yu X; Department of Gastroenterology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Gong P; Department of Gastroenterology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Wang X; Department of Gastroenterology, The Third Xiangya Hospital, Central South University, Changsha, China.
  • Tian L; Department of Gastroenterology, The Third Xiangya Hospital, Central South University, Changsha, China.
Front Pharmacol ; 13: 780179, 2022.
Article in En | MEDLINE | ID: mdl-35330829
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Front Pharmacol Year: 2022 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies Language: En Journal: Front Pharmacol Year: 2022 Document type: Article Affiliation country: China