Nitric oxide-stimulated increase in intracellular cGMP modulates gap junction coupling in rat neocortex

Neuroreport. 1996 Jan 31;7(2):569-72. doi: 10.1097/00001756-199601310-00046.

Abstract

In the present study we demonstrate that gap junction coupling between developing layer II/III pyramidal cells in rat sensorimotor cortex is strongly modified by the nitric oxide (NO)/cyclic guanosine monophosphate (cGMP) system. Dye coupling was revealed by intracellular injection of the gap junction-permeable tracer neurobiotin into single neurones. Following incubation of slices with sodium nitroprusside, a source of NO, the size of dye-coupled cell clusters was significantly reduced. In many cases, 2-3 cells remained strongly dye-coupled. These effects were blocked by intracellular injection of the guanylyl cyclase inhibitor cystamine and mimicked by both application of the membrane-permeant cGMP analogue 8-Br-cGMP and intracellular injection of cGMP. cGMP injection also induced a 60% increase in neuronal input resistance. These results indicate that NO modulates gap junction coupling in the developing neocortex via stimulation of guanylyl cyclase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biotin / analogs & derivatives
  • Cerebral Cortex / drug effects*
  • Cerebral Cortex / metabolism
  • Cyclic GMP / analogs & derivatives
  • Cyclic GMP / metabolism
  • Cyclic GMP / pharmacology
  • Cyclic GMP / physiology*
  • Female
  • Gap Junctions / drug effects*
  • Male
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Nitric Oxide / pharmacology*
  • Nitroprusside / pharmacology
  • Patch-Clamp Techniques
  • Pyramidal Cells / drug effects
  • Pyramidal Cells / physiology
  • Rats
  • Rats, Wistar

Substances

  • neurobiotin
  • Nitroprusside
  • 8-bromocyclic GMP
  • Nitric Oxide
  • Biotin
  • Cyclic GMP