Role of NF kappa B in an Animal Model of Complex Regional Pain Syndrome-type I (CRPS-I)

Marissa Mos, A Laferriere, M Millecamps, M Pilkington, MCJM Sturkenboom, Frank Huygen, TJ Coderre

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NF kappa B is involved in several pathogenic mechanisms that are believed to underlie the complex regional pain syndrome (CRPS), including ischemia, inflammation and sensitization. Chronic postischemia pain (CPIP) has been developed as an animal model that mimics the symptoms of CRPS-I. The possible involvement of NF kappa B in CRPS-I was studied using CPIP rats. Under sodium pentobarbital anesthesia, a tourniquet was placed around the rat left ankle joint, producing 3 hours of ischemia, followed by rapid reperfusion (IR injury). NF kappa B was measured in nuclear extracts of muscle and spinal cord tissue using ELISA. Moreover, the anti-allodynic (mechanical and cold) effect was tested for systemic, intrathecal, or intraplantar treatment with the NF kappa B inhibitor pyrrolidine clithiocarbamate (PDTC). At 2 and 48 hours after IR injury, NF kappa B was elevated in muscle and spinal cord of CPIP rats compared to shams. At 7 days, NF kappa B levels were normalized in muscle, but still elevated in spinal cord tissue. Systemic PDTC treatment relieved mechanical and cold allodynia in a dose-dependent manner, lasting for at least 3 hours. Intrathecal-but not intraplantar-administration also relieved mechanical allodynia. The results suggest that muscle and spinal NF kappa B plays a role in the pathogenesis of CPIP and potentially of human CRPS. Perspective: Using the CPIP model, we demonstrate that NF kappa B is involved in the development of allodynia after a physical injury (ischemia and reperfusion) without direct nerve trauma. Since CPIP animals exhibit many features of human CRPS-I, this observation indicates a potential role for NF kappa B in human CRPS. (C) 2009 by the American Pain Society
Original languageUndefined/Unknown
Pages (from-to)1161-1169
Number of pages9
JournalJournal of Pain
Issue number11
Publication statusPublished - 2009

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  • EMC NIHES-03-77-02

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