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Attenuating the strength of fearful memories could benefit people disabled by memories of past trauma. Pavlovian conditioning experiments indicate that a retrieval cue can return a conditioned aversive memory to a labile state. However, means to enhance retrieval and render a memory more labile are unknown. We hypothesized that augmenting synaptic signaling during retrieval would increase memory lability. To enhance synaptic transmission, mice inhaled CO to induce an acidosis and activate acid sensing ion channels. Transient acidification increased the retrieval-induced lability of an aversive memory. The labile memory could then be weakened by an extinction protocol or strengthened by reconditioning. Coupling CO inhalation to retrieval increased activation of amygdala neurons bearing the memory trace and increased the synaptic exchange from Ca-impermeable to Ca-permeable AMPA receptors. The results suggest that transient acidosis during retrieval renders the memory of an aversive event more labile and suggest a strategy to modify debilitating memories.
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http://dx.doi.org/10.7554/eLife.22564 | DOI Listing |
NPJ Sci Learn
August 2025
School of Psychology, Northwest Normal University, Lanzhou, China.
This study investigated the role of offline consolidation, specifically sleep, in transforming memories strengthened by retrieval practice into stable long-term representations. Forty-eight participants learned weakly associated Chinese word pairs via restudy(RS), retrieval practice with feedback (RP), and retrieval practice without feedback (NRP). After encoding, a nap group slept while a wake group remained awake.
View Article and Find Full Text PDFNeuroscience
August 2025
School of Psychological Sciences, University of Tasmania, TAS 7005, Australia; School of Medicine, University of Queensland, Brisbane, QLD 4072, Australia; Center for the Study of Traumatic Stress, Department of Psychiatry, Uniformed Services University School of Medicine, Bethesda, MD, USA. Electro
Post-traumatic stress disorder (PTSD) is characterized by persistent threat-related memories for which there are limited effective treatment options. The N-methyl-D-aspartate (NMDA) receptor-dependent extracellular signal-regulated kinase (ERK) pathway in the lateral amygdala (LA) is necessary for synaptic plasticity, threat memory consolidation and reconsolidation. Disruption of these memories during the reconsolidation window has been proposed as a therapeutic strategy for PTSD, however, no current therapies using this strategy are available.
View Article and Find Full Text PDFFront Cell Neurosci
July 2025
Institute for Advanced Brain Studies, Lomonosov Moscow State University, Moscow, Russia.
In a healthy brain, the reactivation of memories under conditions of novelty leads to their labilization and subsequent reconsolidation. However, if plasticity of the nervous system is reduced reconsolidation mechanisms may be disrupted, leading to weakening and loss of existing memory. We hypothesize that such self-degradation of old memory due to its reactivation in the compromised brain may lead to progressive memory loss in Alzheimer's disease.
View Article and Find Full Text PDFCancer Immunol Immunother
August 2025
Department of Immunology, Mossakowski Medical Research Institute Polish Academy of Sciences, 5 Adolfa Pawinskiego St., 02-106, Warsaw, Poland.
Induction of ferroptosis, an iron-dependent form of regulated cell death, holds promise as a strategy to overcome tumor resistance to conventional therapies and enhance immunotherapy responses. However, while the susceptibility of tumor cells to ferroptosis is extensively studied, limited data exists on the vulnerability of immune cells to disturbed iron balance and lipid peroxidation. Here, we found that T-cell stimulation rewires iron and redox homeostasis and by increasing levels of reactive oxygen species and labile iron promotes lipid peroxidation and T-cells' ferroptosis.
View Article and Find Full Text PDFClin Neuropsychol
July 2025
Regional Assessment and Resource Centre, Queen's University, Kingston, Canada.
Objective: Anecdotally, individuals reporting symptoms of Attention Deficit/Hyperactivity Disorder (AD/HD) seem to have increased over the past few years, particularly since the onset of the Coronavirus disease 2019 (COVID-19) pandemic. As such, this study aimed to objectively investigate the validity of this observation.
Method: Using archival data from 667 students assessed in a University-based clinic between 2018 and 2024, self-reported AD/HD symptoms on the Conners' Adult AD/HD Rating Scales-Self-Report: Long Version (CAARS-S:L) were compared across three time periods: pre-COVID ( = 407), during COVID ( = 110), and post-COVID ( = 150).