Evidence map›Paper›PMID 41291824›Full record

ArticleBehavioral and brain functions : BBF2025

Sex-dimorphic oxytocin regulation of CA1-dependent spatial memory and synaptic plasticity in juvenile rats.

Evleen Shehadeh, Nisha Rajan Narattil, Milly Kritman, Mouna Maroun

Abstract read
In one paragraph

Article in Behavioral and brain functions : BBF, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Evleen ShehadehSagol Department of Neurobiology, Faculty of Natural Sciences, and the Integrated Brain and Behavior Center, University of Haifa, Haifa, Israel.
Nisha Rajan NarattilSagol Department of Neurobiology, Faculty of Natural Sciences, and the Integrated Brain and Behavior Center, University of Haifa, Haifa, Israel.
Milly KritmanSagol Department of Neurobiology, Faculty of Natural Sciences, and the Integrated Brain and Behavior Center, University of Haifa, Haifa, Israel.
Mouna MarounSagol Department of Neurobiology, Faculty of Natural Sciences, and the Integrated Brain and Behavior Center, University of Haifa, Haifa, Israel. mmaroun@univ.haifa.ac.il.

Funding

Israel Science Foundation 212/24
6 · The paper itself

Abstract

Research into memory mechanisms has predominantly centered on adult male rodents, often overlooking the influences of sex and developmental stage. Memory processes vary significantly between juveniles and adults, with sex acting as a critical determinant. Oxytocin (OXT) has emerged as a key modulator of fear responses and extinction in a sex-dependent manner, with prepubertal females displaying OXT-dependent contextual extinction patterns akin to adult males. These differences likely stem from diverse trajectories of hippocampal and prefrontal cortex maturation. This study examines the CA1 region's involvement in object location memory (OLM), social recognition memory (SRM), and synaptic plasticity among juvenile male and female rats, focusing on OXT's role. Results reveal that, in juvenile (postnatal day -PND 27) protein synthesis inhibition or OXT receptor blockade with OXT receptor antagonist (OXTR-Ant) in CA1 impairs OLM and impairs long-term potentiation (LTP) uniquely in males. These findings correlate with a greater increase in CA1 c-Fos expression following OLM in juvenile males compared to females. The SRM impairment was uniform across sexes under these treatments. In adults (PND 69), OXTR-Ant caused OLM impairment solely in females. These findings underscore pronounced sex- and age-specific variations in CA1-dependent memory and synaptic plasticity, shedding light on distinct neurobiological mechanisms that emerge pre-puberty and evolve throughout development.

Indexed as

CA1 Region, HippocampalNeuronal PlasticityOxytocinSpatial MemoryAnimalsFemaleLong-Term PotentiationMaleRatsReceptors, OxytocinRecognition, PsychologySex CharacteristicsOxytocinReceptors, OxytocinHippocampusJuvenilityObject location memoryPlasticitySex-dimorphism

Identifiers

PMID41291824
PMCPMC12648793

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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 OpenQuestion graph.