Effect of Naringin on Monosodium Iodoacetate-Induced Osteoarthritis Pain in Rats

Med Sci Monit. 2017 Aug 2:23:3746-3751. doi: 10.12659/msm.902396.

Abstract

BACKGROUND The aim of the current study was to evaluate the anti-osteoarthritic and anti-inflammatory effect of naringin in a monosodium iodoacetate (MIA)- induced osteoarthritis (OA) model in rats. The anti-osteoarthritic potential of naringin was evaluated against the MIA-induced OA rat model. MATERIAL AND METHODS Wistar rats were used for the study and were divided into the following groups: normal control (saline-treated); group II (MIA-treated): group III (MIA+Naringin), and group IV (MIA+Indomethacin). The potential effect of naringin was evaluated via its effect on the level of proinflammatory cytokines, measuring the weight-bearing distribution, and histopathological analysis. RESULTS The anti-inflammatory effect of naringin was assessed in vitro in lipopolysaccharide-induced RAW 264.6 cells. The results suggest that naringin exerts an anti-inflammatory effect via reducing the production of the prostaglandin E2 (PGE2), nitric oxide (NO), interlukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) in LPS-induced RAW cells. Additionally, naringin also supported the recovery of hind-limb weight-bearing, reduced the generation or production of inflammatory mediator and proinflammatory cytokines, and protected the tissue from the damage in the OA model. CONCLUSIONS Naringin appears to be an effective therapeutic drug for the treatment of the OA and OA-related symptoms.

MeSH terms

  • Animals
  • Cytokines / blood
  • Cytokines / metabolism
  • Dinoprostone / blood
  • Dinoprostone / metabolism
  • Flavanones / pharmacology
  • Flavanones / therapeutic use*
  • Inflammation / blood
  • Inflammation / complications
  • Inflammation / drug therapy
  • Inflammation / pathology
  • Inflammation Mediators / metabolism
  • Iodoacetates
  • Lipopolysaccharides
  • Male
  • Mice
  • Nitric Oxide / metabolism
  • Osteoarthritis / blood
  • Osteoarthritis / chemically induced*
  • Osteoarthritis / complications
  • Osteoarthritis / drug therapy*
  • Pain / blood
  • Pain / complications
  • Pain / drug therapy*
  • Pain / pathology
  • RAW 264.7 Cells
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Weight-Bearing

Substances

  • Cytokines
  • Flavanones
  • Inflammation Mediators
  • Iodoacetates
  • Lipopolysaccharides
  • Nitric Oxide
  • Dinoprostone
  • naringin