C-FOS ANTISENSE OLIGODEOXYNUCLEOTIDE OFFSETS BEHAVIORAL NOCICEPTIVE RESPONSES AND BOTH UP-REGULATIONS OF C-FOS PROTEIN AND DYNORPHIN A (1-8) IN DORSAL HORN: A STUDY USING THE FORMALIN TEST IN RATS

REFERENCES

• Bullit E. Expression of c-fos-like protein as a marker for neuronal activity following noxious stimulation in the rat. Journal of Comparative Neurology 1990; 296: 517–530
   PubMed Web of Science ®Google Scholar
• Chiasson B. J., Hooper M. L., Murphy P. R., Robertson H. A. Antisense oligonucleotide eliminates in vivo expression of c-fos in mammalian brain. European Journal of Pharmacology 1992; 227: 451–453
   PubMed Web of Science ®Google Scholar
• Civelli O., Douglass J., Goldstein A., Herberu E. Sequence and expression of the rat prodynorphin gene. Proceedings of the National Academy of Science USA 1985; 82: 4291–4295
   PubMedGoogle Scholar
• Doucet S. P., Squinto S. P., Bazan N. G. Fos-Jun and the primary genomic response in the nervous system: Possible physiological role and pathophysiological significance. Molecular neurobiology, N. G. Bazan. Humana, Clifton, NJ 1990; 27–55
   Google Scholar
• Draisci G., Iadorala M. J. Temporal analysis of increases in c-fos, preprodynorphin and prepproenkaphalin mRNAs in rat spinal cord. Molecular Brain Research 1989; 6: 31–37
   PubMedGoogle Scholar
• Dubner R., Ruda M. A. Activity-dependent neuronal plasticity following tissue injury and inflammation. Trends in Neuroscience 1992; 15: 96–103
   PubMed Web of Science ®Google Scholar
• Gillardon F., Beck H., Uhlmann F., Herdegen T., Sandkuhler J., Peyman A., Zimmermann M. Inhibition of c-fos protein expression in rat spinal cord by antisense oligodeoxynucleotide superfusion. European Journal of Neuroscience 1994; 6: 880–884
   Google Scholar
• Hsu S. M., Raind L., Fanger H. Use of avidin-biotin-peroxidase complex (ABC) in immunoperoxidase technique. A comparison technique. A comparison between ABC and unlabeled antibody procedures. Journal of Histochemistry and Cytochemistry 1981; 29: 577–580
   PubMed Web of Science ®Google Scholar
• Hunt S. P., Pini A., Evan G. Induction of c-fos-like protein in spinal cord neurons following sensory stimulation. Nature 1987; 328: 632–634
   PubMed Web of Science ®Google Scholar
• Hunter J. C., Woodburn V. L., Durieux C., Pettersson E. K. E., Poat J. A., Hughes J. C-fos antisense oligodeoxynucleotide increases formalin-induced nociception and regulates formalin-induced nociception and regulates preprodydnorphin expression. Neuroscience 1995; 65: 485–492
   PubMedGoogle Scholar
• Hylden J. L. K., Naphin R. L., Traub R. Effects of spinal kappa-opioid receptor agonists on the responsiveness of nociceptive superficial dorsal horn neurons. Pain 1991; 44: 187–193
   Google Scholar
• Iadarola M. J., Brady L. S., Draisci G., Dubner R. Enhancement of dynorphin gene expression in spinal cord following experimental inflammation: Stimulus specificity, behavioral parameters and opioid receptor binding. Pain 1988; 35: 313–326
   PubMed Web of Science ®Google Scholar
• Kolaj M., Cerne R., Jiang M. C., Lathorn T. H., Randic M. The effects of dynorphin A (1-13) on glutamate and synaptic responses of rat spinal dorsal horn neurons. Society of Neuroscience Abstracts 1992; 18: 281
   Google Scholar
• Lee W. T., Sohn M. L., Park S. H., Ahn S. K., Lee J. E., Park K. A. Studies on the changes of c-fos protein in spinal cord and neurotransmitter in dorsal root ganglion of the rat with an experimental peripheral neuropathy. Yonsei Med. J. 2001; 42: 30–40
   Google Scholar
• Leighton G. E., Hill R. G., Hughes J. Intrathecal injection of a k opioid agonist produces hyperalgesia in the guinea pig. European Journal of Pharmacology 1988; 157: 241–242
   Google Scholar
• Menetrey D., Gannon A., Levine J. D., Basbaum A. I. Expression of c-fos protein in interneuron and projection neurons of the rat spinal cord in response to noxious somatic, articular, and visceral stimulation. Journal of Comp. Neurol. 1989; 285: 177–195
   PubMed Web of Science ®Google Scholar
• Millan M. S. Descending control of pain. Prog. in Neurobiology 2002; 66: 355–474
   PubMed Web of Science ®Google Scholar
• Morgan J. I., Curran T. Stimulus-transcription coupling in neurons: Role of cellular immediate early genes. Trends in Neuroscience 1989; 12: 459–462
   PubMed Web of Science ®Google Scholar
• Nahin R. L., Hylden J. L. K., Humprhrey E. Demonstration of dynorphin A (1–8) immunoreactive axons contacting spinal cord projection neurons in a rat model of peripheral inflammation and hyperalgesia. Pain 1992; 51: 135–143
   Google Scholar
• Naranjo J. R., Mellstrom B., Achaval M., Sasson-Corsi P. Molecular pathways of pain: Fos/jun-mediated activation of noncanoical AP-1 site in the prodynorphin gene. Neuron 1991; 6: 607–617
   PubMedGoogle Scholar
• Noguchi K., Kowalski K., Traub R., Solodkin A., Iadarola M. J., Ruda M. A. Dynorphin expression and Fos-like immunoreactivity following inflammation induced hyperalgesia are colocalized in spinal cord neurons. Molecular Brain Research 1991; 10: 227–233
   PubMedGoogle Scholar
• Presley R. W., Menetrey D., Levine J. D., Basbaum A. I. Systemic morphine suppresses noxious stimulus-evoked Fos protein-like immunoreactivity in the rat spinal cord. Journal of Neuroscience 1990; 10: 323–335
   PubMed Web of Science ®Google Scholar
• Quintero L., Cuest M. C., Silva J. A., Arcaya J. L., Pinerua-Suhaibar L., Maixner W., Suarez-Roca H. Repeated swim stress increases pain-induced expression of c-Fos in the rat lumbar cord. Brain Research 2003; 965: 259–268, [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Ruda M. A., Iadarola M. J., Cohen L. V., Young W. S. In situ hybridization histochemistry and immunocytochemistry reveal an increase in spinal dynorphin biosynthesis in a rat model of peripheral inflammation and hyperalgesia. Proceedings of the National Academy of Science USA 1988; 85: 622–626
   PubMedGoogle Scholar
• Shu S. J. G., Fan L. The glucose oxidase-DAB-nickel method in peroxidase histochemistry of the nervous system. Neuroscience Letters 1988; 85: 161–171
   Google Scholar
• Tjolsen A., Berg O.-G., Hunskaar S., Rosland J. H., Hol K. The formalin tests: An evaluation of the method. Rev. Pain 1992; 51: 5–17
   PubMed Web of Science ®Google Scholar
• Wahlestedt C. Antisense oligonucleotide strategies in neuropharmacology. Trends Pharmacol. Science 1994; 15: 42–46
   PubMed Web of Science ®Google Scholar
• Wahlestedt C., Golanov E., Yamamoto S., Yee F., Erecson H., Yoo H., Inturrisi C. E., Reis D. J. Antisense oligodeoxynucleotides to NMDA-R1 receptor channel protect cortical neurons from excitotoxicity and reduce focal ischaemic infarctions. Nature 1993; 363: 260–263, [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Wang H., Liu R. J., Zhang R. X., Qiao J. T. Peripheral NMDA receptors contribute to activation of nociceptors: a c-fos expression study in rats. Neuroscience Letters 1997; 221: 101–104, [PUBMED], [INFOTRIEVE]
   Google Scholar
• Wheeler-Aceto H., Cowan A. Standardization of the rat paw formalin test for the evaluation of analgesics. Psychopharmacology 1991; 104: 35–44, [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Yaksh T. L., Rudy T. A. Chronic catheterization of the spinal subarachnoid space. Physiol. Behav. 1976; 17: 1031–1036, [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar
• Zhang R. X., Chen J. Y., Maryann A. Ruda. Functional relationships between peripheral inflammation thermal hyperalgesia and enhanced dynorphin gene expression in spinal cord of rat: behavioral and mRNA studies. Chin. J. Neuroanat. 1999; 15: 19–26
   Google Scholar
• Zhang R.-X., Wang R., Chen J.-Y., Qiao J.-T. Effects of descending inhibitory systems on the c-fos expression in the rat spinal cord during formalin-induced noxious stimulation. Neuroscience 1994; 58: 299–304, [PUBMED], [INFOTRIEVE]
   PubMed Web of Science ®Google Scholar