2008
DOI: 10.1093/bja/aem398
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Inflammation-induced up-regulation of ionotropic glutamate receptor expression in human skin

Abstract: These results, in human tissue, demonstrate that iGluR mRNA and protein expression are increased during persistent inflammation and that this increased activity may be involved in mediating clinical inflammatory pain in human skin.

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Cited by 18 publications
(8 citation statements)
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“…These glutamate receptor populations are up-regulated in inflamed human skin [86] and appear to be involved in sensitizing primary afferent nociceptors during inflammation and tissue injury [6]. For example, during inflammation, intraplantar injection of NMDA aggravated mechanical and thermal hyperalgesia and boosted the excitability of nociceptive afferents in the inflamed rat paw [23].…”
Section: Discussionmentioning
confidence: 99%
“…These glutamate receptor populations are up-regulated in inflamed human skin [86] and appear to be involved in sensitizing primary afferent nociceptors during inflammation and tissue injury [6]. For example, during inflammation, intraplantar injection of NMDA aggravated mechanical and thermal hyperalgesia and boosted the excitability of nociceptive afferents in the inflamed rat paw [23].…”
Section: Discussionmentioning
confidence: 99%
“…[ 6 7 ] NMDA receptors are found in peripheral nerves and the central nervous system. [ 8 9 ] Magnesium is also an antagonist of the NMDA receptor ion channel. [ 10 ] We planned to study the efficacy of magnesium sulfate nebulization to reduce the incidence of POST.…”
Section: Introductionmentioning
confidence: 99%
“…132 Furthermore, it was shown that (1) glutamate-like immunoreactivity increased in the epidermis and dermis of the inflamed human skin, 133 (2) the number of sensory axons containing iGluRs increased during inflammation in the rat model, 134 and (3) mRNA as well as protein levels for NMDA, AMPA, and KA receptors were up-regulated in clinically inflamed human skin. 135 This may contribute to the development of peripheral sensitization in inflammation and emphasizes the importance of glutamate receptor signaling in inflammatory pain. In line with this, it was recently reported that peripheral administration of an mGluR5 antagonist attenuated not only inflammation but also MO-induced nociceptive behavior in the craniofacial masseter muscle.…”
Section: Glutamate Signaling In Head and Neck Areasmentioning
confidence: 99%