Evidence map›Paper›PMID 42049944›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2026

Lasting effects of early-life oxytocin treatment on LTP and episodic memory in a mouse model of Fragile X syndrome.

Jasmine Chavez, Aliza A Le, Julie C Lauterborn, Brittney M Cox, Yousheng Jia, Gary Lynch, Christine M Gall

Abstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 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. Article
  2. The how and why for multiple forms of hippocampal LTP.Frontiers in synaptic neuroscience · 2026
    Review
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

7 authors.

Jasmine Chavez *Department of Anatomy and Neurobiology, University of California, Irvine, CA, USA.
Aliza A Le *Department of Anatomy and Neurobiology, University of California, Irvine, CA, USA.
Julie C LauterbornDepartment of Anatomy and Neurobiology, University of California, Irvine, CA, USA.ORCID http://orcid.org/0000-0002-8444-6151
Brittney M CoxDepartment of Anatomy and Neurobiology, University of California, Irvine, CA, USA.ORCID http://orcid.org/0000-0002-7118-5300
Yousheng JiaDepartment of Anatomy and Neurobiology, University of California, Irvine, CA, USA.
Gary LynchDepartment of Anatomy and Neurobiology, University of California, Irvine, CA, USA. ga.s.lynch@gmail.com.ORCID http://orcid.org/0000-0002-3520-8544
Christine M GallDepartment of Anatomy and Neurobiology, University of California, Irvine, CA, USA. cmgall@uci.edu.ORCID http://orcid.org/0000-0002-7727-796X

Funding

Impact of Cannabinoid Across the Lifespan (ICAL)P50DA044118 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI Stephen Vincent Mahler · 2018 to 2026
$18.2M
Institute for Clinical and Translational ScienceUM1TR004927 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI DAN M COOPER, Eric J. Vilain · 2024 to 2026
$12.2M
Epilepsy Research Training ProgramT32NS045540 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Tallie Z. Baram, Robert F Hunt · 2003 to 2026
$4.9M
Epigenetic mechanisms in the medial habenula governing drug-seeking behaviorR01DA047441 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI LYNCH, GARY S, WOOD, MARCELO ANDRES · 2020 to 2024
$3.3M
Postnatal Oxytocin Treatment and Cognitive Function in FragileXR01HD101642 · NICHD · UNIVERSITY OF CALIFORNIA-IRVINE · PI GALL, CHRISTINE M, LYNCH, GARY S · 2021 to 2025
$2.5M
Yale University Clinical and Translational Science Award ProgramTL1TR000141 · NCATS · YALE UNIVERSITY · PI SHERWIN, ROBERT S · 2012 to 2015
$720k
Institute for Clinical and Translational Science NRSA Postdoctoral Research Training CoreT32TR005459 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI VINCENT James CAIOZZO, Anand K Ganesan · 2025 to 2026
$340k
Comunidad Autónoma de la Región de Murcia (Regional Health Authorities of Murcia) DA047441NCATS NIH HHS T32 TR005459NCATS NIH HHS TL1 TR000141NCATS NIH HHS UM1 TR004927NICHD NIH HHS R01 HD101642NIDA NIH HHS P50 DA044118NIDA NIH HHS R01 DA047441NINDS NIH HHS T32 NS045540United States Department of Defense | United States Navy | Office of Naval Research (ONR) N00014-24-1-2014U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) HD101642U.S. Department of Health & Human Services | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) HD101642-S1U.S. Department of Health & Human Services | NIH | National Center for Advancing Translational Sciences (NCATS) TR00141U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) NS04554U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) DA044118U.S. Department of Health & Human Services | NIH | National Institute on Drug Abuse (NIDA) DA047441
6 · The paper itself

Abstract

Deficits in episodic memory are a debilitating feature of Fragile X syndrome (FXS) and other congenital autism spectrum disorders (ASDs). There is evidence that oxytocin (OXT) treatments can improve sociability in persons with ASD and related animal models, encouraging the idea that benefits might extend to cognitive function. We tested this possibility in male FXS model, Fmr1-knockout (KO) mice. Intranasal treatments with OXT or saline were given daily during the second or fifth postnatal week, and effects on social behavior, spatial and episodic memory, and hippocampal synaptic plasticity were assessed in adulthood. Saline-treated Fmr1-KOs exhibited profound deficits in social recognition, object location memory, what-when-where components of episodic memory and long-term potentiation (LTP) in both the CA3-CA1 and lateral perforant path (LPP) systems; NMDAR-mediated components of LPP responses were also impaired. OXT treatments during the second week postnatal normalized all of these functions in Fmr1-KOs assessed in adulthood; this included restoration of initial stages of CA3-CA1 LTP and granule cell NMDAR-mediated currents. In hippocampal slices from naïve adult male Fmr1-KO mice, bath-applied OXT treatment restored LTP in CA1 but not the LPP, indicating pathway-specific effects. Intranasal OXT treatments during the 5

Indexed as

Fragile X SyndromeLong-Term PotentiationMemory, EpisodicOxytocinAdministration, IntranasalAnimalsAnimals, NewbornDisease Models, AnimalFragile X Messenger Ribonucleoprotein 1HippocampusMaleMiceMice, Inbred C57BLMice, KnockoutSocial BehaviorFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1Oxytocin

Identifiers

PMID42049944
PMCPMC13536618

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.