Fear conditioning occludes late-phase long-term potentiation at thalamic input synapses onto the lateral amygdala in rat brain slices

Neurosci Lett. 2012 Jan 6;506(1):121-5. doi: 10.1016/j.neulet.2011.10.063. Epub 2011 Nov 2.

Abstract

Late-phase long-term potentiation (L-LTP) of excitatory synaptic transmission at thalamic input synapses onto the lateral amygdala (T-LA synapses) has been proposed as a cellular substrate for long-term fear memory. This notion is evidenced primarily by previous reports in which the same pharmacological treatments block both T-LA L-LTP and the consolidation of fear memory. In this study, we report that fear conditioning occludes L-LTP at T-LA synapses in brain slices prepared after fear memory consolidation. L-LTP was restored either when synaptic depotentiation was induced prior to L-LTP induction in brain slices prepared from conditioned rats or when brain slices were prepared from conditioned rats that had been exposed to subsequent fear extinction, which is a behavior paradigm known to induce in vivo synaptic depotentiation at T-LA synapses. These results suggest that fear conditioning recruits L-LTP-like mechanisms that are reversible and saturable at T-LA synapses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amygdala / cytology*
  • Animals
  • Biophysics
  • Conditioning, Psychological / physiology*
  • Electric Stimulation
  • Extinction, Psychological / physiology
  • Fear*
  • In Vitro Techniques
  • Long-Term Potentiation / drug effects
  • Long-Term Potentiation / physiology*
  • Male
  • Methoxyhydroxyphenylglycol / analogs & derivatives
  • Methoxyhydroxyphenylglycol / pharmacology
  • Neural Pathways / physiology
  • Neurons / cytology
  • Neurons / physiology
  • Patch-Clamp Techniques / methods
  • Rats
  • Rats, Sprague-Dawley
  • Synapses / drug effects
  • Synapses / physiology*
  • Thalamus / cytology*
  • Time Factors

Substances

  • Methoxyhydroxyphenylglycol
  • 3,4-dihydroxyphenylglycol