4.5 Article

Involvement of spinal cord nuclear factor κB activation in rat models of proinflammatory cytokine-mediated pain facilitation

Journal

EUROPEAN JOURNAL OF NEUROSCIENCE
Volume 22, Issue 8, Pages 1977-1986

Publisher

WILEY
DOI: 10.1111/j.1460-9568.2005.04379.x

Keywords

allodynia; gp120; inhibitory factor kappa B; proinflammatory cytokines; nuclear factor kappa B; Sprague-Dawley rats

Categories

Funding

  1. NIDA NIH HHS [DA015642] Funding Source: Medline
  2. NINDS NIH HHS [NS38020, NS40696, NS40098] Funding Source: Medline

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Proinflammatory cytokines, such as interleukin-1 beta and tumour necrosis factor-alpha, are released by activated glial cells in the spinal cord and play a major role in pain facilitation. These cytokines exert their actions, at least partially, through the activation of the transcription factor, nuclear factor kappa B (NF-kappa B). In turn, NF-kappa B regulates the transcription of many inflammatory mediators, including cytokines. We have previously shown that intrathecal injection of the human immunodeficiency virus-1 (HIV-1) envelope glycoprotein, gp120, induces mechanical allodynia via the release of proinflammatory cytokines. Here, we investigated whether NF-kappa B is involved in gp120-induced pain behaviour in Sprague-Dawley rats. Intrathecal administration of NF-kappa B inhibitors, pyrrolidinedithiocarbamate (PDTC) and SN50, prior to gp120 partially attenuated gp120-induced allodynia. In addition, PDTC delayed and reversed allodynia in a model of neuropathic pain induced by sciatic nerve inflammation. These observations suggest that intrathecal gp120 may lead to activation of NF-kappa B within the spinal cord. To reveal NF-kappa B activation, we assessed inhibitory factor kappa B alpha (I kappa B alpha) mRNA expression by in situ hybridization, as NF-kappa B activation up-regulates I kappa B alpha gene expression as part of an autoregulatory feedback loop. No or low levels of I kappa B alpha mRNA were detected in the lumbar spinal cord of vehicle-injected rats, whereas I kappa B alpha mRNA expression was markedly induced in the spinal cord following intrathecal gp120 in predominantly astrocytes and endothelial cells. Moreover, I kappa B alpha mRNA expression positively correlated with proinflammatory cytokine protein levels in lumbosacral cerebrospinal fluid. Together, these results demonstrate that spinal cord NF-kappa B activation is involved, at least in part, in exaggerated pain states.

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