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Inhibition of peripheral vanilloid TRPV1 receptors reduces noxious heat‐evoked responses of dorsal horn neurons in naïve, carrageenan‐inflamed and neuropathic rats
Author(s) -
Jhaveri Maulik D.,
Elmes Steven J. R.,
Kendall David A.,
Chapman Victoria
Publication year - 2005
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/j.1460-9568.2005.04227.x
Subject(s) - trpv1 , chemistry , nociception , noxious stimulus , nociceptor , neuropathic pain , capsaicin , receptor , peripheral , pharmacology , endocrinology , carrageenan , medicine , transient receptor potential channel , biochemistry
The vanilloid TRPV1 receptor, present on primary afferent fibres, is activated by noxious heat, low pH and endogenous vanilloids. Changes in the function or distribution of TRPV1 receptors may play an important role in pain induced by inflammation or neuropathy. The aim of the present study was to evaluate the role of peripheral TRPV1 receptors in thermal nociception in rat models of inflammatory and neuropathic pain. Here, we have determined the effects of peripheral administration of the potent TRPV1 receptor antagonist iodoresiniferatoxin (IRTX) on noxious heat (45 °C)‐evoked responses of spinal wide dynamic range (WDR) neurons in naïve, carrageenan‐inflamed, sham‐operated and L5/6 spinal nerve‐ligated (SNL) anaesthetized rats in vivo . In addition, effects of peripheral administration of IRTX on mechanically evoked responses of WDR neurons were determined in sham‐operated and SNL rats. Carrageenan inflammation significantly ( P < 0.05) increased the 45 °C‐evoked responses of WDR neurons. Intraplantar injection of the lower dose of IRTX (0.004 µg) inhibited ( P < 0.05) 45 °C‐evoked responses of WDR neurons in carrageenan‐inflamed, but not in naïve, rats. The higher dose of IRTX (0.4 µg) significantly ( P < 0.05) inhibited 45 °C‐evoked responses in both inflamed and naïve rats. In sham‐operated and SNL rats, IRTX (0.004 and 0.4 µg) significantly ( P < 0.05) inhibited 45 °C‐evoked, but had no effect on mechanically evoked responses of WDR neurons. These data support the role of peripheral TRPV1 receptors in noxious thermal transmission in naïve, inflamed and neuropathic rats, and suggest that there is an increased functional contribution of peripheral TRPV1 receptors following acute inflammation.