5-HT1A receptors modulate small-conductance Ca2+-activated K+ channels

J Neurosci Res. 2004 Dec 15;78(6):845-54. doi: 10.1002/jnr.20318.

Abstract

Small-conductance calcium-activated potassium channels (SK) are responsible for the medium afterhyperpolarisation (mAHP) following action potentials in neurons. Here we tested the ability of serotonin (5-HT) to modulate the activity of SK channels by coexpressing 5-HT1A receptors with different subtypes of SK channels (SK1, SK2, and SK3) in Xenopus laevis oocytes. SK channels were activated by intracellular injection of Cd2+. Subsequent activation of 5-HT1A receptors by 8-OH-DPAT always produced an inhibition of the SK current, showing the existence of a specific pathway between the receptor and the ion channel. To investigate the physiological relevance of this pathway, we characterized the mAHP present after action potentials in spinal motoneurons recorded in a slice preparation from the lumbar spinal cord of the adult turtle. By performing current and voltage clamp recordings, we showed that 8-OH-DPAT specifically inhibited the fraction of the AHP mediated by SK channels. We conclude that the activity of SK channels is modulated by activation of serotonergic receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 8-Hydroxy-2-(di-n-propylamino)tetralin / pharmacology
  • Animals
  • Apamin / pharmacology
  • Cloning, Molecular
  • Female
  • Humans
  • Oocytes / drug effects
  • Oocytes / physiology
  • Potassium Channels, Calcium-Activated / physiology*
  • Rats
  • Receptor, Serotonin, 5-HT1A / drug effects
  • Receptor, Serotonin, 5-HT1A / physiology*
  • Recombinant Proteins / drug effects
  • Recombinant Proteins / metabolism
  • Xenopus laevis

Substances

  • Potassium Channels, Calcium-Activated
  • Recombinant Proteins
  • Receptor, Serotonin, 5-HT1A
  • Apamin
  • 8-Hydroxy-2-(di-n-propylamino)tetralin