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Updated: Mar 10, 2026

Disrupting Reconsolidation of Fear Memory in Humans by a Noradrenergic β-Blocker
Published on: December 18, 2014
Cued memory reconsolidation in rats requires nitric oxide
Natalia V Bal1, Mariia P Rysakova1, Alia Kh Vinarskaya1
1Institute of Higher Nervous Activity and Neurophysiology, Russian Academy of Sciences, 5A Butlerova St., Moscow, 117485, Russia.
Nitric oxide (NO) plays a key role in destabilizing fear memories during reconsolidation. Blocking NO synthesis prevents memory destabilization, suggesting a novel therapeutic target for fear memory modification.
Area of Science:
- Neuroscience
- Molecular Biology
- Behavioral Science
Background:
- Memory reconsolidation requires protein synthesis after reactivation.
- Reactivated memories become labile and susceptible to modification.
- Nitric oxide (NO) is implicated in various neuronal processes.
Purpose of the Study:
- To investigate the role of nitric oxide (NO) in the destabilization of fear memory during reconsolidation.
- To determine if inhibiting NO synthesis affects memory reconsolidation.
Main Methods:
- Rats underwent fear conditioning and memory reactivation under protein synthesis blockade.
- Selective nitric oxide synthase (NOS) blockers (3-Br-7-NI, ARL) were administered.
- Memory retention was assessed to evaluate destabilization.
Main Results:
- Administration of NOS blockers prevented the destabilization of fear memory.
- Inhibition of NO synthesis during reactivation blocked memory impairment.
- These findings highlight NO's role in memory destabilization.
Conclusions:
- The nitric oxide (NO) signaling pathway is crucial for fear memory destabilization upon reactivation.
- Disrupting NO signaling during reconsolidation can prevent alterations in long-term fear memory.
- Targeting NO pathways may offer a strategy to modify fear memories.
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