Cued memory reconsolidation in rats requires nitric oxide

Eur J Neurosci. 2017 Mar;45(5):643-647. doi: 10.1111/ejn.13503. Epub 2017 Jan 9.

Abstract

It is well-known that the reactivation of consolidated fear memory under boundary conditions of novelty and protein synthesis blockade results in an impairment of memory, suggesting that the reactivated memory is destabilized and requires synthesis of new proteins for reconsolidation. We tested the hypothesis of nitric oxide (NO) involvement in memory destabilization during the reconsolidation process in rats using memory reactivation under different conditions. We report that administration of NO-synthase selective blockers 3-Br-7-NI or ARL in the conditions of reactivation of memory under a protein synthesis blockade prevented destabilization of fear memory to the conditioned stimulus. Obtained results support the role of NO signaling pathway in the destabilization of existing fear memory triggered by reactivation, and demonstrate that the disruption of this pathway during memory reconsolidation may prevent changes in long-term memory.

Keywords: labilization; memory; nitric oxide; protein synthesis; reactivation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amidines / pharmacology
  • Animals
  • Cues*
  • Enzyme Inhibitors / pharmacology
  • Fear
  • Indazoles / pharmacology
  • Male
  • Memory Consolidation / drug effects*
  • Nitric Oxide / metabolism*
  • Nitric Oxide Synthase / antagonists & inhibitors
  • Rats
  • Rats, Wistar

Substances

  • 3-bromo-7-nitroindazole
  • ARL 17477
  • Amidines
  • Enzyme Inhibitors
  • Indazoles
  • Nitric Oxide
  • Nitric Oxide Synthase