Plasticity in fast synaptic inhibition of adult oxytocin neurons caused by switch in GABA(A) receptor subunit expression

Neuron. 1997 Nov;19(5):1103-14. doi: 10.1016/s0896-6273(00)80401-8.

Abstract

We found that magnocellular oxytocin neurons in adult female rats exhibit an endogenous GABA(A) receptor subunit switch around parturition: a decrease in alpha1:alpha2 subunit mRNA ratio correlated with a decrease in allopregnanolone potentiation and increase in decay time constant of the GABA(A) receptor-mediated IPSCs in these cells. The causal relationship between changes in alpha1:alpha2 mRNA ratio and the ion channel kinetics was confirmed using in vitro antisense deletion. Further, GABA(A) receptors exhibited a tonic inhibitory influence upon oxytocin release in vivo, and allopregnanolone helped to restrain oxytocin neuron in vitro firing only before parturition, when the alpha1:alpha2 subunit mRNA ratio was still high. Such observations provide evidence for the physiological significance of GABA(A) receptor subunit heterogeneity and plasticity in the adult brain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Electric Conductivity
  • Electrophysiology
  • Female
  • GABA Modulators / pharmacology
  • Labor, Obstetric / metabolism
  • Neural Inhibition / physiology*
  • Neuronal Plasticity / physiology*
  • Neurons / physiology*
  • Oxytocin / metabolism*
  • Pregnancy
  • Pregnancy, Animal / metabolism*
  • Pregnanolone / pharmacology
  • RNA, Messenger / metabolism
  • Rats
  • Receptors, GABA-A / drug effects
  • Receptors, GABA-A / genetics
  • Receptors, GABA-A / metabolism*
  • Supraoptic Nucleus / cytology
  • Supraoptic Nucleus / metabolism
  • Synapses / metabolism
  • Synapses / physiology*
  • Time Factors

Substances

  • GABA Modulators
  • RNA, Messenger
  • Receptors, GABA-A
  • Oxytocin
  • Pregnanolone