Protein kinase C-mediated enhancement of glycine response in rat sacral dorsal commissural neurones by serotonin

J Physiol. 1996 Oct 15;496 ( Pt 2)(Pt 2):491-501. doi: 10.1113/jphysiol.1996.sp021701.

Abstract

1. The modulatory effect of serotonin (5-hydroxytryptamine, 5-HT), on the glycine (Gly) response was investigated in neurones acutely dissociated from the rat sacral dorsal commissural nucleus (SDCN) using a nystatin-perforated patch recording configuration. 2. 5-HT potentiated the 10(-5) M Gly-induced Cl- current (IGly) in a concentration-dependent manner without changing the reversal potential of the Gly response or the affinity of Gly to its receptor. 3. alpha-Methyl-5-HT mimicked and ketanserine blocked the 5-HT action on IGly, thus indicating the 5-HT2 receptor-mediated enhancement. 4. Phorbol-12-myristate-13-acetate and 1-oleoyl-2-acetylglycerol potentiated IGly. The subsequent application of 5-HT slightly increase IGly. Chelerythrine blocked the enhancement of IGly by 5-HT, thus suggesting the involvement of protein kinase C (PKC) in the pathway of 5-HT action on IGly. 5. Pertussis toxin (IAP) treatment did not block the facilitatory effect of 5-HT on IGly. 6. BAPTA AM did not disturb the 5-HT-induced potentiation of IGly, thus suggesting that [Ca2+]i is not involved in the 5-HT effect. 7. In conclusion, activation of a 5-HT2 receptor coupled to an IAP-insensitive G-protein increases intracellular diacylglycerol (DAG) formation. The accumulation of DAG also increases the Ca(2+)-independent PKC activity, thus resulting in the potentiation of the Gly response in the SDCN neurones.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / physiology
  • Chelating Agents / pharmacology
  • Electrophysiology
  • GTP-Binding Proteins / metabolism
  • In Vitro Techniques
  • Neurons / drug effects
  • Neurons / physiology*
  • Patch-Clamp Techniques
  • Protein Kinase C / physiology*
  • Rats
  • Rats, Wistar
  • Receptors, Glycine / drug effects
  • Receptors, Glycine / physiology*
  • Receptors, Serotonin / drug effects
  • Receptors, Serotonin / physiology
  • Serotonin / pharmacology*
  • Serotonin Antagonists / pharmacology
  • Serotonin Receptor Agonists / pharmacology
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Spinal Cord / cytology
  • Spinal Cord / drug effects
  • Spinal Cord / physiology*

Substances

  • Chelating Agents
  • Receptors, Glycine
  • Receptors, Serotonin
  • Serotonin Antagonists
  • Serotonin Receptor Agonists
  • Serotonin
  • Protein Kinase C
  • GTP-Binding Proteins
  • Calcium