Potential of Raloxifene in reversing osteoarthritis-like alterations in rat chondrocytes: an in vitro model study

J Biosci. 2013 Mar;38(1):135-47. doi: 10.1007/s12038-012-9282-7.

Abstract

The aim of this study was to investigate the effects of Raloxifene (Ral) on degeneration-related changes in osteoarthritis (OA)-like chondrocytes using two- and three-dimensional models. Five-azacytidine (Aza-C) was used to induce OA-like alterations in rat articular chondrocytes and the model was verified at molecular and macrolevels. Chondrocytes were treated with Ral (1, 5 and 10 mu M) for 10 days. Caspase-3 activity, gene expressions of aggrecan, collagen II, alkaline phosphatase (ALP), collagen X, matrix metalloproteinases (MMP-13, MMP-3 and MMP-2), and MMP-13, MMP-3 and MMP-2 protein expressions were studied in two-dimensional model. Matrix deposition and mechanical properties of agarose-chondrocyte discs were evaluated in three-dimensional model. One mu M Ral reduced expression of OA-related genes, decreased apoptosis, and MMP-13 and MMP-3 protein expressions. It also increased aggrecan and collagen II gene expressions relative to untreated OA-like chondrocytes. In three-dimensional model, 1 mu M Ral treatment resulted in increased collagen deposition and improved mechanical properties, although a significant increase for sGAG was not observed. In summation, 1 mu M Ral improved matrix-related activities, whereas dose increment reversed these effects except ALP gene expression and sGAG deposition. These results provide evidence that low-dose Ral has the potential to cease or reduce the matrix degeneration in OA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggrecans / genetics
  • Aggrecans / metabolism
  • Alkaline Phosphatase / genetics
  • Alkaline Phosphatase / metabolism
  • Animals
  • Apoptosis / drug effects
  • Azacitidine
  • Biomarkers / metabolism
  • Bone Density Conservation Agents / pharmacology*
  • Cartilage, Articular / drug effects*
  • Cartilage, Articular / metabolism
  • Cartilage, Articular / pathology
  • Caspase 3 / genetics
  • Caspase 3 / metabolism
  • Chondrocytes / drug effects*
  • Chondrocytes / metabolism
  • Chondrocytes / pathology
  • Collagen Type II / genetics
  • Collagen Type II / metabolism
  • Dose-Response Relationship, Drug
  • Gene Expression / drug effects*
  • Matrix Metalloproteinases / genetics
  • Matrix Metalloproteinases / metabolism
  • Models, Biological
  • Osteoarthritis / chemically induced
  • Osteoarthritis / metabolism
  • Osteoarthritis / pathology
  • Primary Cell Culture
  • Raloxifene Hydrochloride / pharmacology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Aggrecans
  • Biomarkers
  • Bone Density Conservation Agents
  • Collagen Type II
  • Raloxifene Hydrochloride
  • Alkaline Phosphatase
  • Caspase 3
  • Matrix Metalloproteinases
  • Azacitidine