Pain related behaviour in two models of osteoarthritis in the rat knee

• Published in: Pain (Amsterdam) Vol. 112; no. 1; pp. 83 - 93
• Main Authors: Fernihough, Janet, Gentry, Clive, Malcangio, Marzia, Fox, Alyson, Rediske, John, Pellas, Theodore, Kidd, Bruce, Bevan, Stuart, Winter, Janet
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 01.11.2004; Elsevier
• Subjects: Analgesics; Analgesics - pharmacology; Analgesics - therapeutic use; Animals; Biological and medical sciences; Diclofenac; Disease Models, Animal; Diseases of the osteoarticular system; Gabapentin; Hindlimb; Male; Medical sciences; Morphine; Neuropharmacology; Osteoarthritis; Osteoarthritis, Knee - drug therapy; Osteoarthritis, Knee - physiopathology; Pain - complications; Pain - drug therapy; Pain - pathology; Pain Measurement - methods; Pain Threshold - drug effects; Pain Threshold - physiology; Paracetamol; Pharmacology. Drug treatments; Rats; Rats, Wistar; p.o; Paracetamol; OA; Gabapentin; NSAIDs; Morphine; s.c; DRGs; PWT; Diclofenac; Allodynia; Knee; Animal model; Rat; Rodentia; Diseases of the osteoarticular system; Joint; Hyperalgesia; Osteoarticular system; Analgesia; Vertebrata; Mammalia; Analgesic; Pain; Meniscectomy; Gahapentin; Arthropathy; Degenerative disease; Osteoarthritis
• ISSN: 0304-3959; 1872-6623
• DOI: 10.1016/j.pain.2004.08.004

Osteoarthritis (OA) is a major healthcare burden, with increasing incidence. Pain is the predominant clinical feature, yet therapy is ineffective for many patients. While there are considerable insights into the mechanisms underlying tissue remodelling, there is poor understanding of the link between disease pathology and pain. This is in part owing to the lack of animal models that combine both osteoarthritic tissue remodelling and pain. Here, we provide an analysis of pain related behaviours in two models of OA in the rat: partial medial meniscectomy and iodoacetate injection. Histological studies demonstrated that in both models, progressive osteoarthritic joint pathology developed over the course of the next 28 days. In the ipsilateral hind limb in both models, changes in the percentage bodyweight borne were small, whereas marked mechanical hyperalgesia and tactile allodynia were seen. The responses in the iodoacetate treated animals were generally more robust, and these animals were tested for pharmacological reversal of pain related behaviour. Morphine was able to attenuate hyperalgesia 3, 14 and 28 days after OA induction, and reversed allodynia at days 14 and 28, providing evidence that this behaviour was pain related. Diclofenac and paracetamol were effective 3 days after arthritic induction only, coinciding with a measurable swelling of the knee. Gabapentin varied in its ability to reverse both hyperalgesia and allodynia. The iodoacetate model provides a basis for studies on the mechanisms of pain in OA, and for development of novel therapeutic analgesics.