Gumiganghwal-tang ameliorates cartilage destruction via inhibition of matrix metalloproteinase

J Ethnopharmacol. 2020 Oct 28:261:113074. doi: 10.1016/j.jep.2020.113074. Epub 2020 Jun 10.

Abstract

Ethnopharmacological relevance: Kyung-Bang Gumiganghwal-tang tablet (GMGHT) is a standardized Korean Medicine that could treat a cold, headache, arthralgia and fever. Although GMGHT has been used for arthritis-related diseases including a sprain, arthralgia, unspecified arthritis and knee arthritis, there is no pre-clinical evidence to treat osteoarthritis (OA). This study determined the drug dosage and the mechanisms of GMGHT for OA.

Methods: OA was induced by intra-articular monoiodoacetic acid (MIA) injection in Sprague-Dawley rats. As calculated from the human equivalent dose formula, GMGHT was orally administered at the doses of 9.86, 98.6 and 986 mg/kg for 4 weeks. The arthritis score was performed by a blind test, and histological changes in articular cartilage were indicated by hematoxylin and eosin, Safranin O and toluidine blue staining. SW1353 chondrocytes were stimulated by interleukin (IL)-1β recombinant to analyze the expressions of Type II collagen, matrix metalloproteinases (MMPs) and nuclear factor (NF)-κB.

Results: Rough and punctate surfaces of the femoral condyle induced by MIA, were recovered by the GMGHT treatment. The arthritis score was significantly improved in the 968 mg/kg of GMGHT-treated cartilage. Loss of chondrocytes and proteoglycan were ameliorated at the deep zone of the subchondral bone plate by the GMGHT administration in OA rats. The expression of Type II collagen was increased, while MMP-1, -3 and -13 levels were decreased in the GMGHT-treated SW1353 chondrocytes. In addition, the GMGHT treatment regulated NF-κB activation along with IL-6, transforming growth factor-β and IL-12 production.

Conclusions: GMGHT promoted the recovery of articular cartilage damage by inhibiting MMPs, accompanied with its anti-inflammatory effects in OA. GMGHT might be an alternative therapeutic treatment for OA.

Keywords: Chondrocyte; Gumiganghwal-tang; Matrix metalloproteinase; Osteoarthritis.

MeSH terms

  • Animals
  • Arthritis, Experimental / chemically induced
  • Arthritis, Experimental / enzymology
  • Arthritis, Experimental / pathology
  • Arthritis, Experimental / prevention & control*
  • Cartilage, Articular / drug effects*
  • Cartilage, Articular / enzymology
  • Cartilage, Articular / pathology
  • Cell Line, Tumor
  • Chondrocytes / drug effects
  • Chondrocytes / enzymology
  • Chondrocytes / pathology
  • Collagen Type II / metabolism
  • Cytokines / metabolism
  • Humans
  • Inflammation Mediators / metabolism
  • Iodoacetic Acid
  • Joints / drug effects*
  • Joints / enzymology
  • Joints / pathology
  • Male
  • Matrix Metalloproteinase 1 / metabolism
  • Matrix Metalloproteinase 13 / metabolism
  • Matrix Metalloproteinase 3 / metabolism
  • Matrix Metalloproteinase Inhibitors / pharmacology*
  • Matrix Metalloproteinases, Secreted / antagonists & inhibitors*
  • Matrix Metalloproteinases, Secreted / genetics
  • Matrix Metalloproteinases, Secreted / metabolism
  • Osteoarthritis / chemically induced
  • Osteoarthritis / enzymology
  • Osteoarthritis / pathology
  • Osteoarthritis / prevention & control*
  • Plant Extracts / pharmacology*
  • Rats, Sprague-Dawley

Substances

  • Collagen Type II
  • Cytokines
  • Inflammation Mediators
  • Matrix Metalloproteinase Inhibitors
  • Plant Extracts
  • kumi-kyokatsu-to
  • Matrix Metalloproteinase 13
  • Matrix Metalloproteinases, Secreted
  • Mmp13 protein, rat
  • Matrix Metalloproteinase 3
  • MMP1 protein, rat
  • Matrix Metalloproteinase 1
  • Iodoacetic Acid