Regulation of Proinflammatory Cytokines Gene Expression by Nociceptin/Orphanin Fq in the Spinal Cord and the Cultured Astrocytes.
From: Department of Integrative Medicine and Neurobiology, Institute of Acupuncture Research, Shanghai Medical College, Fudan University, P.O. Box 291, 138 Yi Xue Yuan Road, Shanghai 200032, China.
Neuroscience
- Publish Date: Jan 2007
- ISSN: 0306-4522
- Volume: 144
- Issue: 1
- Pages: 275-85
- Medium: Print
- Language: English
- Citation (JAMA): Fu X, Zhu Z-H, Wang Y-Q, et al. Regulation of Proinflammatory Cytokines Gene Expression by Nociceptin/Orphanin Fq in the Spinal Cord and the Cultured Astrocytes.. Neuroscience Jan 2007;144:275-85
Abstract
Peripheral inflammation induces central sensitization characterized by the development of allodynia and hyperalgesia to thermal stimuli. Recent evidence suggests that activation of glial cells and a subsequent increase in proinflammatory cytokines contribute to the development of behavioral hypersensitivity after nerve injury or peripheral inflammation. The neuropeptide nociceptin/orphanin FQ (N/OFQ), the endogenous agonist of the N/OFQ peptide receptor (ORL1 receptor), has been demonstrated to play an important role in modulation of nociceptive signals. In the present study, we investigated: (1) astrocyte activation and proinflammatory cytokine expression at the lumbar spinal cord following intraplantar administration of complete Freund’s adjuvant (CFA) in rats; (2) the mechanism of N/OFQ on nociception modulation, the relationship between N/OFQ and cytokines in the rat CNS in vivo and in vitro. The results showed: (1) CFA-induced peripheral inflammation evoked robust astrocyte activation and proinflammatory cytokines spinally; (2) down-regulation of cytokine mRNA transcripts by intrathecal administration of N/OFQ, the effects produced by N/OFQ were abolished by combination with ORL1 receptor-specific antagonist [Nphe(1)]N/OFQ(1-13)NH2; (3) ORL1 receptor was expressed on astrocytes of rat spinal cord; (4) cytokine gene expression was inhibited in astrocyte cultures exposed to N/OFQ, the inhibiting effects of N/OFQ were significantly blocked by [Nphe(1)]N/OFQ(1-13)NH2. The present data demonstrated that astrocyte activation and enhanced cytokine expression at the CNS had a role in eliciting behavioral hypersensitivity; the anti-nociception function of N/OFQ might be dependent on cytokines derived from astrocytes, the effects were attributable to the ORL1 receptor pathway.
Mesh Headings (Keywords): Animals, Astrocytes, Behavior, Animal, Blotting, Western, Cells, Cultured, Cytokines, Foot, Freund’s Adjuvant, Gene Expression Regulation, Glial Fibrillary Acidic Protein, Heat, Immunohistochemistry, Inflammation, Injections, Injections, Spinal, Interleukin-1beta, Interleukin-6, Male, Opioid Peptides, Pain Threshold, RNA, Messenger, Rats, Rats, Sprague-Dawley, Receptors, Opioid, Reverse Transcriptase Polymerase Chain Reaction, Spinal Cord, Tumor Necrosis Factor-alpha
Check for Full Text / PubMed Unique Identifier (PMID): 17069983
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