Evidence map›Paper›PMID 41215998›Full record

ArticleIBRO neuroscience reports2025

Oxytocin enhances neurogenesis and synaptic plasticity to attenuate age-related cognitive decline in aged mice.

Mi Hee Shin, Zhan Zhi Yin, Kyeong-No Yoon, Qing-Ling Quan, Dong Hun Lee, Jin Ho Chung

Abstract read
In one paragraph

Article in IBRO neuroscience reports, 2025. 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

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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.

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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

6 authors.

Mi Hee ShinDepartment of Dermatology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
Zhan Zhi YinDepartment of Dermatology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
Kyeong-No YoonDepartment of Dermatology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
Qing-Ling QuanDepartment of Dermatology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
Dong Hun LeeDepartment of Dermatology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.
Jin Ho ChungDepartment of Dermatology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain aging is characterized by progressive structural and functional deterioration, leading to cognitive decline and impaired social functioning. A key factor in this process is the age-related decline in adult neurogenesis, particularly in the hippocampal dentate gyrus, which is linked to deficits in learning, memory, and increased social anxiety. Oxytocin, a neuropeptide synthesized in the hypothalamus, regulates social behavior, cognition, and emotion by acting on brain regions including the hippocampus. Importantly, oxytocin levels decrease with age, potentially contributing to cognitive impairment. Here, we examined whether chronic intraperitoneal oxytocin administration could attenuate cognitive decline in aged mice. Twelve-month-old mice received oxytocin injections (0.5 mg/kg) five times weekly for 13 weeks. Behavioral testing at 12 weeks of treatment using the object-place recognition task showed enhanced spatial learning and recognition memory in oxytocin-treated mice compared with saline controls. Immunohistochemistry revealed significantly increased doublecortin (DCX)-positive cells in the hippocampus, indicating enhanced neurogenesis. Furthermore, oxytocin treatment upregulated the expression of glutamate receptor 1 (GluR1) and N-methyl-D-aspartate receptor subunit 2B (NMDAR2B), which are markers of synaptic plasticity. These findings suggest that chronic oxytocin treatment is associated with enhanced neurogenesis and synaptic plasticity, which may contribute to improved cognition in aged mice. Our results support oxytocin as a potential therapeutic agent for age-related cognitive decline.

Indexed as

Cognitive functionNeurogenesisOxytocinSynaptic plasticity

Identifiers

PMID41215998
PMCPMC12597284

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