Bioactive fractions from Securidaca inappendiculata alleviated collagen-induced arthritis in rats by regulating metabolism-related signaling

Kaohsiung J Med Sci. 2020 Jul;36(7):523-534. doi: 10.1002/kjm2.12205. Epub 2020 Mar 18.

Abstract

Securidaca inappendiculata is a xanthone rich medicinal plant that has been used in the treatment of inflammation and autoimmune diseases like rheumatoid arthritis (RA) for centuries; however, the material base and mechanism of action responsible for its anti-arthritis effect still remains elusive. The objective of this study is to evaluate the therapeutic effects of xanthone-enriched extract of the plant against collagen-induced arthritis (CIA) in rats and explore the underlying mechanisms. The xanthone-deprived fraction (XDF) and xanthone-rich fraction (XRF) were obtained by using a resin adsorption coupled with acid-base treatment method, and their chemical composition difference was characterized by UPLC-MS/MS analysis. Effects of the two on CIA were analyzed using radiographic, histological, and immunohistochemical analyses. The results indicated that XRF alleviated joint structures destructions with the higher efficacy than XDF, and decreased levels of TNF-α, IL-6, and anti-cyclic citrullinated peptide antibody in CIA rats significantly. Furthermore, XRF inhibited nicotinamide phosphoribosyl transferase (NAMPT) mediated fat biosynthesis and utilization indicated by clinical evidences and metabonomics analysis, which thereby disrupted energy-metabolism feedback. In addition, Toll-like Receptor 4 and High Mobility Group Protein 1 expressions were downregulated in XRF-treated CIA rats. Collective evidences suggest NAMPT could be an ideal target for RA treatments and reveal a novel antirheumatic mechanism of S. inappendiculata by regulating NAMPT controlled fat metabolism.

Keywords: energy metabolism; inflammation; rheumatoid arthritis; xanthone.

MeSH terms

  • Animals
  • Anti-Citrullinated Protein Antibodies / genetics
  • Anti-Citrullinated Protein Antibodies / immunology
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology*
  • Arthritis, Experimental / chemically induced
  • Arthritis, Experimental / drug therapy*
  • Arthritis, Experimental / genetics
  • Arthritis, Experimental / immunology
  • Chemical Fractionation / methods
  • Collagen Type II / administration & dosage
  • Cytokines / antagonists & inhibitors*
  • Cytokines / genetics
  • Cytokines / immunology
  • Freund's Adjuvant / administration & dosage
  • Gene Expression Regulation
  • HMGB1 Protein / antagonists & inhibitors
  • HMGB1 Protein / genetics
  • HMGB1 Protein / immunology
  • Interleukin-6 / antagonists & inhibitors
  • Interleukin-6 / genetics
  • Interleukin-6 / immunology
  • Lipid Metabolism / drug effects*
  • Lipid Metabolism / genetics
  • Male
  • Nicotinamide Phosphoribosyltransferase / antagonists & inhibitors*
  • Nicotinamide Phosphoribosyltransferase / genetics
  • Nicotinamide Phosphoribosyltransferase / immunology
  • Plant Extracts / chemistry
  • Rats
  • Rats, Sprague-Dawley
  • Securidaca / chemistry*
  • Signal Transduction
  • Toll-Like Receptor 4 / antagonists & inhibitors
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / immunology
  • Treatment Outcome
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology
  • Xanthones / isolation & purification
  • Xanthones / pharmacology*

Substances

  • Anti-Citrullinated Protein Antibodies
  • Anti-Inflammatory Agents
  • Collagen Type II
  • Cytokines
  • HMGB1 Protein
  • Hbp1 protein, rat
  • Il6 protein, rat
  • Interleukin-6
  • Plant Extracts
  • Tlr4 protein, rat
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Xanthones
  • Freund's Adjuvant
  • xanthone
  • Nicotinamide Phosphoribosyltransferase
  • nicotinamide phosphoribosyltransferase, rat