| Literature DB >> 30594691 |
Hanwen Chen1, Hui Lin2, Shujun Xie3, Bo Huang3, Yufeng Qian4, Kelie Chen2, Yuequn Niu3, Han-Ming Shen5, Jianting Cai6, Peiwei Li6, Jianhang Leng7, Hao Yang3, Dajing Xia8, Yihua Wu9.
Abstract
Myricetin is a plant-derived flavonoid that exhibits diverse pharmacological properties. The NLRP3 (NLR family, pyrin domain-containing 3 protein) inflammasome is a cytosolic multiprotein complex that plays a critical role in the innate immune response and pathogenesis of multiple inflammatory disorders. The present study found that myricetin inhibited NLRP3 inflammasome assembly via promotion of reactive oxygen species (ROS)-independent ubiquitination of NLRP3 and reduction of ROS-dependent ubiquitination of ASC (apoptosis-associated speck-like protein containing a CARD), which disrupted the interaction between ASC and NLRP3 and inhibited ASC oligomerization. This effect was further confirmed in vivo using mouse models of lipopolysaccharide (LPS)-induced sepsis and alum-induced peritonitis. These results suggest the therapeutic value of myricetin by targeting NLRP3-driven inflammatory diseases.Entities:
Keywords: Myricetin; NLRP3 inflammasome; Reactive oxygen species; Ubiquitination
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Year: 2018 PMID: 30594691 DOI: 10.1016/j.taap.2018.12.019
Source DB: PubMed Journal: Toxicol Appl Pharmacol ISSN: 0041-008X Impact factor: 4.219