Co-localized GABA and somatostatin use different ionic mechanisms to hyperpolarize target neurons in the lamprey spinal cord

Neurosci Lett. 1991 Dec 16;134(1):93-7. doi: 10.1016/0304-3940(91)90516-v.

Abstract

gamma-Aminobutyric acid (GABA) and somatostatin are co-localized in cells close to the central canal in the lamprey. These cells project to the lateral margin of the spinal cord where they form a GABA and somatostatin containing plexus. Stretch receptor neurons (edge cells) are situated along the lateral margin of the spinal cord and their dendrites extend into the GABA and somatostatin containing plexus. To investigate whether GABA and/or somatostatin exert an affect on edge cells, these putative transmitters were applied from extracellular pipettes onto edge cells during intracellular recordings. Both GABA and somatostatin hyperpolarized the edge cells but through different ionic mechanisms. GABA activated a chloride current while somatostatin activated a current most likely carried by potassium which, however, could not be blocked by any of the conventional potassium blockers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chloride Channels
  • Chlorides / metabolism
  • Fluorescent Antibody Technique
  • Ion Channel Gating / drug effects
  • Lampreys / physiology*
  • Mechanoreceptors / drug effects*
  • Membrane Proteins / drug effects
  • Neurons / drug effects
  • Potassium / metabolism
  • Potassium Channels / drug effects
  • Somatostatin / pharmacology*
  • Somatostatin / physiology
  • Spinal Cord / physiology*
  • gamma-Aminobutyric Acid / pharmacology*
  • gamma-Aminobutyric Acid / physiology

Substances

  • Chloride Channels
  • Chlorides
  • Membrane Proteins
  • Potassium Channels
  • Somatostatin
  • gamma-Aminobutyric Acid
  • Potassium