1. Actinidia arguta extract attenuates inflammasome activation: Potential involvement in NLRP3 ubiquitination.
- Author
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Heo KH, Sun X, Shim DW, Kim MK, Koppula S, Yu SH, Kim HB, Kim TJ, Kang TB, and Lee KH
- Subjects
- Animals, Anti-Inflammatory Agents therapeutic use, Caspase 1 metabolism, Cells, Cultured, Female, Interleukin-1beta metabolism, Lipopolysaccharides pharmacology, Macrophages drug effects, Macrophages metabolism, Mice, Inbred C57BL, Peritonitis chemically induced, Peritonitis drug therapy, Peritonitis metabolism, Plant Extracts therapeutic use, Plant Leaves, Ubiquitination, Uric Acid, Actinidia, Anti-Inflammatory Agents pharmacology, Inflammasomes metabolism, NLR Family, Pyrin Domain-Containing 3 Protein metabolism, Plant Extracts pharmacology
- Abstract
Ethnopharmacological Relevance: Actinidia arguta (A. arguta) has been widely used in Asian countries as a traditional medicinal herb to treat inflammation-related diseases, such as gastritis, bronchitis, and arthritis., Aim of the Study: The inhibitory effect of A. arguta leaves' extract (AA) on inflammasome activation was investigated to verify its traditional use in treating inflammation-related diseases., Materials and Methods: Bone marrow-derived macrophages (BMDMs) primed by lipopolysaccharide (LPS) were activated by selective inflammasome stimulators, and the effect of AA on inflammasome activation was investigated. A monosodium urate crystal (MSU)-induced peritonitis mouse model was used to study the in vivo efficacy of AA on inflammasome activation., Results: In the in vitro study, AA regulated NLRP3 ubiquitination and apoptosis-associated speck-like protein containing a CARD (ASC) oligomerization, leading to the inhibition of NLRP3 inflammasome-mediated interleukin (IL)-1β secretion. The inhibitory effect of AA on inflammasome activation in vitro was further confirmed in vivo using an MSU-induced peritonitis mouse model., Conclusion: AA provided scientific evidence, substantiating the traditional claims for its use in the treatment of inflammation and inflammation-mediated metabolic disorders, including gout., (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Published
- 2018
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