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      Sensory and vascular changes in a rat monoarthritis model: prophylactic and therapeutic effects of meloxicam

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          Abstract

          Objective and design

          The objective of this study was to determine the ability of meloxicam prophylaxis and therapy to blunt the effect of complete Freund’s adjuvant (CFA) induced monoarthritis.

          Materials and methods

          First the validity of this animal model was established by examining joint changes at multiple levels after injecting CFA into the tibio-tarsal joint. Next, meloxicam (5 mg/kg) or vehicle was administered on days 0–7 (prophylactic) and on days 7–16 (therapeutic) in separate groups of animals.

          Results

          The CFA-injected joint demonstrated hallmark histological and structural changes such as pannus formation, bone remodeling, cartilage erosion and immune cell infiltration. Both prophylactic and therapeutic treatment with meloxicam effectively reduced swelling (ankle circumference), oedema and extravasation of Evans blue dye in the affected joint. Moreover, meloxicam reduced loss in range of motion and also reduced mechanical stimulus evoked pain scores. Notably, these effects persisted after discontinuing drug treatment.

          Conclusion

          The present study provides a unique comparison of prophylactic versus therapeutic effects of meloxicam in the CFA-induced model of monoarthritis.

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          Author and article information

          Contributors
          Journal
          9508160
          8759
          Inflamm Res
          Inflamm. Res.
          Inflammation research : official journal of the European Histamine Research Society ... [et al.]
          1023-3830
          1420-908X
          15 November 2016
          28 March 2010
          August 2010
          01 December 2016
          : 59
          : 8
          : 667-678
          Affiliations
          Department of Physiology and Pharmacology, University of Western Ontario, London, ON, Canada. Institute of Medical Science, University of Toronto, Toronto, Canada
          Department of Physiology and Pharmacology, University of Western Ontario, London, ON, Canada
          Robarts Research Institute, University of Western Ontario, London, ON, Canada. Department of Surgery, University of Western Ontario, London, ON, Canada
          Department of Physiology and Pharmacology, University of Western Ontario, London, ON, Canada
          Author notes

          Present Address: J. A. Hashmi, Division of Brain, Imaging and Behaviour–Systems, Neuroscience, Toronto Western Research Institute, University Health Network, Toronto, Canada

          Present Address: K. Yashpal, Pain Research Laboratories, McMaster University, 1200 Main St. West, HSC 4N35, Hamilton, ON L8N 3Z5, Canada

          Present Address: J. L. Henry, Departments of Psychiatry and Behavioural Neurosciences, and Anaesthesia, McMaster University, 1200 Main St. West, HSC 4N35, Hamilton, ON L8N 3Z5, Canada

          Article
          PMC5132625 PMC5132625 5132625 capmc419
          10.1007/s00011-010-0179-3
          5132625
          20349327
          71e1fe19-0947-48c9-8a13-e935dd8ee7a8
          History
          Categories
          Article

          Joint pain,Range of motion,CFA,Rheumatoid arthritis,Animal model,Inflammatory joint disease

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