Multiple spine boutons are formed after long-lasting LTP in the awake rat

Brain Struct Funct. 2014 Jan;219(1):407-14. doi: 10.1007/s00429-012-0488-0. Epub 2012 Dec 6.

Abstract

The formation of multiple spine boutons (MSBs) has been associated with cognitive abilities including hippocampal-dependent associative learning and memory. Data obtained from cultured hippocampal slices suggest that the long-term maintenance of synaptic plasticity requires the formation of new synaptic contacts on pre-existing synapses. This postulate however, has never been tested in the awake, freely moving animals. In the current study, we induced long-term potentiation (LTP) in the dentate gyrus (DG) of awake adult rats and performed 3-D reconstructions of electron micrographs from thin sections of both axonal boutons and dendritic spines, 24 h post-induction. The specificity of the observed changes was demonstrated by comparison with animals in which long-term depression (LTD) had been induced, or with animals in which LTP was blocked by an N-methyl-D-aspartate (NMDA) antagonist. Our data demonstrate that whilst the number of boutons remains unchanged, there is a marked increase in the number of synapses per bouton 24 h after the induction of LTP. Further, we demonstrate that this increase is specific to mushroom spines and not attributable to their division. The present investigation thus fills the gap existing between behavioural and in vitro studies on the role of MSB formation in synaptic plasticity and cognitive abilities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biophysics
  • Computer Simulation
  • Dendritic Spines / physiology*
  • Dendritic Spines / ultrastructure
  • Electric Stimulation
  • Electrodes, Implanted
  • Excitatory Amino Acid Antagonists / pharmacology
  • Hippocampus / cytology*
  • Hippocampus / physiology*
  • Long-Term Potentiation / drug effects
  • Long-Term Potentiation / physiology*
  • Long-Term Synaptic Depression / drug effects
  • Long-Term Synaptic Depression / physiology
  • Male
  • Nerve Net / physiology
  • Nerve Net / ultrastructure
  • Piperazines / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Synapses / physiology*
  • Synapses / ultrastructure
  • Time Factors
  • Wakefulness*

Substances

  • Excitatory Amino Acid Antagonists
  • Piperazines
  • 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid