Evidence map›Paper›PMID 42436993›Full record

ArticleiScience2026

Hippocampal ERK2 dimerization regulates inhibitory avoidance memory reconsolidation and synaptic plasticity.

Santiago Ojea Ramos, Candela Medina, María Del Carmen Krawczyk, Julieta Millan, María Florencia Acutain, Arturo Gabriel Romano, María Verónica Baez, Francisco José Urbano, Mariano Martín Boccia, Mariana Feld

Abstract read
In one paragraph

Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. The pERKs of temporal order memory in mice.Frontiers in molecular neuroscience · 2026
    Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Santiago Ojea RamosUniversidad de Buenos Aires (UBA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE), Buenos Aires, Argentina.
Candela MedinaUniversidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Fisiología, Biología Molecular y Celular, Buenos Aires, Argentina.
María Del Carmen KrawczykUniversidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Fisiología, Biología Molecular y Celular, Buenos Aires, Argentina.
Julieta MillanUniversidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Cátedra de Farmacología. Laboratorio de Neurofarmacología de Procesos de Memoria, Buenos Aires, Argentina.
María Florencia AcutainUniversidad de Buenos Aires (UBA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Biología Celular y Neurociencias "Prof. Dr. E. de Robertis" (IBCN), Buenos Aires, Argentina.
Arturo Gabriel RomanoUniversidad de Buenos Aires (UBA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE), Buenos Aires, Argentina.
María Verónica BaezUniversidad de Buenos Aires (UBA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Biología Celular y Neurociencias "Prof. Dr. E. de Robertis" (IBCN), Buenos Aires, Argentina.
Francisco José UrbanoUniversidad de Buenos Aires (UBA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE), Buenos Aires, Argentina.
Mariano Martín BocciaUniversidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Cátedra de Farmacología. Laboratorio de Neurofarmacología de Procesos de Memoria, Buenos Aires, Argentina.
Mariana FeldUniversidad de Buenos Aires (UBA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Instituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE), Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extensive research has examined extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation in memory and synaptic plasticity, yet the mechanisms linking ERK activity to memory stabilization remain unclear. ERK dimerization is required for the activation of cytoplasmic targets involved in plasticity. Here, we investigated the role of ERK2 dimerization in long-term memory reconsolidation and synaptic plasticity. Reactivation of weak inhibitory avoidance (wIA) memory significantly reduced hippocampal ERK2 dimerization. Post-reactivation, intrahippocampal infusion of the ERK dimerization inhibitor DEL-22379 (DEL) produced bidirectional effects, impairing reconsolidation of strong inhibitory avoidance (sIA) memory, while enhancing reconsolidation of wIA memory. DEL administration efficiently blocked hippocampal ERK2 dimerization and impaired maintenance of high-frequency stimulation-induced long-term potentiation (LTP) in the hippocampal slices. These findings demonstrate that ERK2 dimerization occurs in the intact mouse brain and plays a critical role in IA memory and synaptic plasticity, highlighting its relevance in memory reconsolidation processes.

Indexed as

DEL-22379long-term potentiationMAPK signalingmemory retrievalmemory strength

Identifiers

PMID42436993
PMCPMC13355786

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.