Molecular mechanisms of pain: serotonin1A receptor agonists trigger transactivation by c-fos of the prodynorphin gene in spinal cord neurons

Neuron. 1993 Apr;10(4):599-611. doi: 10.1016/0896-6273(93)90163-l.

Abstract

By using spinal cord neurons cultured in chemically defined medium, a double labeling procedure, and blockage with antisense oligonucleotides, we show that induction of c-fos and the subsequent transactivation of the prodynorphin gene are coupled events, triggered by serotonin1A receptor agonists. Addition of the specific 1A agonist 8-hydroxy-2-(di-n-propylamino)-tetralin (8-OH-DPAT) to the culture, at concentrations similar to that needed for transactivation of the prodynorphin gene, also significantly increases cAMP levels. Furthermore, in rats depleted of serotonin by intrathecal administration of 5,7-dihydroxytryptamine, the induction of prodynorphin after noxious stimulation is dramatically decreased compared with the induction in sham-operated rats. These results suggest that the expression of the prodynorphin gene in spinal cord is under the control of the raphe-spinal efferents containing serotonin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 8-Hydroxy-2-(di-n-propylamino)tetralin / pharmacology
  • Afferent Pathways / physiology
  • Animals
  • Base Sequence
  • Cells, Cultured
  • Denervation
  • Enkephalins / genetics*
  • Gene Expression Regulation
  • Genes
  • Molecular Sequence Data
  • Neurons / physiology
  • Oligonucleotide Probes / genetics
  • Pain / physiopathology*
  • Protein Precursors / genetics*
  • Proto-Oncogene Proteins c-fos / physiology*
  • Receptors, Serotonin / physiology*
  • Spinal Cord / cytology
  • Spinal Cord / physiology*
  • Transcriptional Activation*

Substances

  • Enkephalins
  • Oligonucleotide Probes
  • Protein Precursors
  • Proto-Oncogene Proteins c-fos
  • Receptors, Serotonin
  • 8-Hydroxy-2-(di-n-propylamino)tetralin
  • preproenkephalin