Anti-inflammatory properties of Morus bombycis Koidzumi via inhibiting IFN-β signaling and NLRP3 inflammasome activation

J Ethnopharmacol. 2015 Dec 24:176:424-8. doi: 10.1016/j.jep.2015.11.022. Epub 2015 Nov 10.

Abstract

Ethnopharmacological relevance: Morus bombycis Koidzumi (M. bombycis, Moraceae) has been used in Asian countries as a traditional medicine for the treatment of hypertension, diabetes, and inflammation-related disorders.

Aim of study: Although its anti-inflammatory actions have been partly documented, scientific evidence involving its molecular mechanisms related to inflammasome activation signaling pathways remains unknown.

Materials and methods: Lipopolysaccharide-stimulated RAW 264.7 cells and bone marrow-derived murine macrophages were used to study the in vitro effect of methanolic extract of M. bombycis (MB) on inflammatory responses. A monosodium urate crystal (MSU)-induced peritonitis murine model was used to study the in vivo effects.

Results: MB attenuated the production of nitric oxide and interleukin-6, through the regulation of the interferon-β receptor signaling pathway. MB also inhibited IL-1β secretion via attenuation of NLRP3 inflammasome activation. Furthermore, MB inhibited MSU-induced peritonitis in the in vivo murine model.

Conclusions: This study provides the key molecular mechanisms involved in the anti-inflammatory effects of M. bombycis, substantiating the traditional claims of its use in the treatment of inflammation-related disorders.

Keywords: Anti-inflammation; Inflammasome; Morus bombycis; Peritonitis; TRIF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Anti-Inflammatory Agents / therapeutic use
  • Carrier Proteins / antagonists & inhibitors*
  • Carrier Proteins / metabolism
  • Cell Line
  • Cells, Cultured
  • Female
  • Inflammasomes
  • Interferon-beta / antagonists & inhibitors*
  • Interferon-beta / metabolism
  • Interleukin-6 / metabolism
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Mice, Inbred C57BL
  • Morus*
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Nitric Oxide / metabolism
  • Peritonitis / chemically induced
  • Peritonitis / drug therapy
  • Peritonitis / metabolism
  • Phytotherapy
  • Plant Extracts / pharmacology*
  • Plant Extracts / therapeutic use
  • Reactive Oxygen Species / metabolism
  • Uric Acid

Substances

  • Anti-Inflammatory Agents
  • Carrier Proteins
  • Inflammasomes
  • Interleukin-6
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Nlrp3 protein, mouse
  • Plant Extracts
  • Reactive Oxygen Species
  • interleukin-6, mouse
  • Uric Acid
  • Nitric Oxide
  • Interferon-beta