Development and pharmacological characterization of a rat model of osteoarthritis painPomonis, James D.*; Boulet, Jamie M.; Gottshall, Susan L.; Phillips, Steve; Sellers, Rani; Bunton, Tracie; Walker, KatharinePAIN: April 2005 - Volume 114 - Issue 3 - p 339–346 doi: 10.1016/j.pain.2004.11.008 Article Buy SDC Abstract Author InformationAuthors Article MetricsMetrics Osteoarthritis (OA) is an age-related joint disease characterized by degeneration of articular cartilage and is associated with chronic pain. Although several experimental models of OA have been employed to investigate the underlying etiologies of the disease, there has been relatively little investigation into development of animal models of OA to study the pain associated with the condition. In the present study, we investigated OA induced by injection of either iodoacetate or papain into the knee joint of rats, and assessed the joint degeneration with radiographic analyses and measured pain behavior using hind limb weight bearing. We found that injection of iodoacetate, but not papain, resulted in a chronic joint degeneration as measured by decreased bone mineral content and bone mineral density, necrosis of articular cartilage and osteophyte formation. These pathological changes were associated with pain that manifested as time- and concentration-dependent alterations in hind limb weight bearing. These alterations in hind limb weight bearing were reversed with morphine, but were not significantly affected by acute administration of either indomethacin or celecoxib. However, administration of 30 mg/kg celecoxib twice daily for 10 days resulted in a significant restoration of hind limb weight bearing. We conclude that the iodoacetate model of OA is a relevant animal model to study pain associated with OA, and can be used to test potential therapeutic agents. Discovery Research, Purdue Pharma, L.P., 6 Cedarbrook Drive, Cranbury, NJ 08512, USA *Corresponding author. Address: 1246 University Ave W, Suite 205, St. Paul, MN 55104, USA. Tel.: +1 651 209 0736; fax: +1 651 209 0727. E-mail: firstname.lastname@example.org Submitted August 3, 2004; revised October 1, 2004; accepted November 8, 2004. © 2005 Lippincott Williams & Wilkins, Inc.