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. 2009 Apr;56(4):419-424.
doi: 10.4097/kjae.2009.56.4.419.

Contralateral allodynia and central change in the chronic post-ischemic pain model rats

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Free article

Contralateral allodynia and central change in the chronic post-ischemic pain model rats

Kyung Hwa Kwak et al. Korean J Anesthesiol. 2009 Apr.
Free article

Abstract

Background: Mirror-image allodynia is a mysterious phenomenon that occurs in association with many clinical pain syndromes including complex regional pain syndromes (CRPS). Underlying mechanisms for the development of such pain are still a matter of investigation. Several studies suggest that activation of the N-methyl-D-aspartate (NMDA) receptor is essential for central sensitization as a base for persistent pain. The aim is to assess whether alteration of NMDA receptor expression correlates with the contralateral allodynia in the chronic post-ischemia pain (CPIP) model rats representing CRPS-Type I.

Methods: Application of a tight-fitting tourniquet for a period of 3 hours before reperfusion produced CPIP in male Sprague-Dawley rats. The mechanical paw withdrawal thresholds to von Frey stimuli (using a dynamic plantar aesthesiometer) were measured as pain indicators in ipsilateral and contralateral hindpaws. Phosphorylation of the NMDA receptor 1 subunit (pNR1), assessed with Western blot, was measured in the contralateral L4-6 spinal cord.

Results: Ipsilateral and contralateral mechanical allodynia is present at 4 hours after reperfusion, peaked at 3 days, and continued for 7 days after reperfusion. The relative density of pNR1 of CPIP rats significantly decreased in the contralateral L4-6 spinal cord compared to baseline value (P < 0.05). There was significant correlation between paw withdrawal threshold and the relative density of pNR1 (ipsilateral; R2 = 0.75, P < 0.01, contralateral; R2 = 0.60, P < 0.01).

Conclusions: These data suggest that pNR1 is correlated to the contralateral mechanical allodynia in CPIP rats.

Keywords: Chronic post-ischemia pain; Complex regional pain syndrome-type I; Mirror-image allodynia; NMDA receptor.

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