Upregulation of IL-6, IL-8 and CCL2 gene expression after acute inflammation: Correlation to clinical pain.

Tissue injury initiates a cascade of inflammatory mediators and hyperalgesic substances including prostaglandins, cytokines and chemokines. Using microarray and qRT-PCR gene expression analyses, the present study evaluated changes in gene expression of a cascade of cytokines following acute inflamma...

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Publicado en:PAIN Vol. 142; no. 3; pp. 275 - 284
Autores principales: Wang XM, Hamza M, Wu TX, Dionne RA, Wang, Xiao-Min, Hamza, May, Wu, Tian-Xia, Dionne, Raymond A
Formato: Journal Article
Publicado: Lippincott Williams & Wilkins Apr2009
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Apr2009
      vid: 142
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      pub: Lippincott Williams & Wilkins
      place: Baltimore, Maryland
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        NLM19233564
        2010223319
        10.1016/j.pain.2009.02.001
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        atl: Upregulation of IL-6, IL-8 and CCL2 gene expression after acute inflammation: Correlation to clinical pain.
      aug:
        au:
          Wang XM
          Hamza M
          Wu TX
          Dionne RA
          Wang, Xiao-Min
          Hamza, May
          Wu, Tian-Xia
          Dionne, Raymond A
        affil: National Institute of Nursing Research, NIH, Building 10, CRC, Room 2-1339, Bethesda, MD 20892, USA
      sug:
        subj:
          Biochemical Phenomena Drug Effects
          Cox-2 Inhibitors Administration and Dosage
          Facial Pain Metabolism
          Inflammation Mediators Metabolism
          Inflammation Metabolism
          Interleukins Metabolism
          Adult
          Facial Pain Prevention and Control
          Female
          Inflammation Prevention and Control
          Male
          Statistics
          Adult: 19-44 years
          Female
          Male
      ab: Tissue injury initiates a cascade of inflammatory mediators and hyperalgesic substances including prostaglandins, cytokines and chemokines. Using microarray and qRT-PCR gene expression analyses, the present study evaluated changes in gene expression of a cascade of cytokines following acute inflammation and the correlation between the changes in the gene expression level and pain intensity in the oral surgery model of tissue injury and acute pain. Tissue injury resulted in a significant upregulation in the gene expression of interleukin-6 (IL-6; 63.3-fold), IL-8 (8.1-fold), chemokine (C-C motif) ligand 2 (CCL2; 8.9-fold), chemokine (C-X-C motif) ligand 1 (CXCL1; 30.5-fold), chemokine (C-X-C motif) ligand 2 (CXCL2; 26-fold) and annexin A1 (ANXA1; 12-fold). The upregulation of IL-6 gene expression was significantly correlated to the upregulation of IL-8, CCL2, CXCL1 and CXCL2 gene expression. Interestingly, the tissue injury-induced upregulation of IL-6, IL-8 and CCL2 gene expression, was positively correlated to pain intensity at 3h post-surgery, the onset of acute inflammatory pain. However, ketorolac treatment did not have a significant effect on the gene expression of IL-6, IL-8, CCL2, CXCL2 and ANXA1 at the same time point of acute inflammation. These results demonstrate that the upregulation of IL-6, IL-8 and CCL2 gene expression contributes to the development of acute inflammation and inflammatory pain. The lack of effect of ketorolac on the expression of these gene products may be related to the ceiling analgesic effects of non-steroidal anti-inflammatory drugs.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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