Evidence map›Paper›PMID 40285336›Full record

ArticleCNS neuroscience & therapeutics2025

Aging-Induced Episodic-Like Memory Impairment Could be Alleviated by Melatonin Treatment via Preserving Blood-Brain Barrier Integrity and Upregulating CRTC1.

Yanping Wang, Xinyu Zhang, Hui Guo, Shuxia Qian, Hailun Fang, Xiaoqiang Wu, Yufei Shen, Congying Xu, Beiqun Zhou, Chun Guo and 3 more

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 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

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. 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

13 authors.

Yanping WangDepartment of Neurology, The Second Affiliated Hospital of Jiaxing University, Jiaxing, China.
Xinyu ZhangInstitute of Neuroscience, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Hui GuoDepartment of Histology and Embryology, School of Basic Medical Sciences, Advanced Innovation Center for Human Brain Protection, Capital Medical University, Beijing, People's Republic of China.
Shuxia QianDepartment of Neurology, The Second Affiliated Hospital of Jiaxing University, Jiaxing, China.
Hailun FangDepartment of Neurology, Bengbu Medical College, Bengbu, China.
Xiaoqiang WuDepartment of Neurology, The Second Affiliated Hospital of Jiaxing University, Jiaxing, China.
Yufei ShenDepartment of Neurology, The Second Affiliated Hospital of Jiaxing University, Jiaxing, China.
Congying XuDepartment of Neurology, The Second Affiliated Hospital of Jiaxing University, Jiaxing, China.
Beiqun ZhouDepartment of Neurology, The Second Affiliated Hospital of Jiaxing University, Jiaxing, China.
Chun GuoSchool of Biosciences, University of Sheffield, Sheffield, UK.ORCID 0000-0002-1540-3166
Xudong LuDepartment of Neurology, The Second Affiliated Hospital of Jiaxing University, Jiaxing, China.
Xiaoling ZhangDepartment of Neurology, The Second Affiliated Hospital of Jiaxing University, Jiaxing, China.
Xinchun JinInstitute of Neuroscience, The Second Affiliated Hospital of Soochow University, Suzhou, China.ORCID 0000-0002-5351-7914

Funding

Health and Family Planning Commission of Zhejiang Province 2022AY30028Jiaxing Plan of Science and Technology 2025CGZ064National Natural Science Foundation of China 81671145National Natural Science Foundation of China 81870973Zhejiang Provincial Natural Science Foundation of China LTGY24H090002
6 · The paper itself

Abstract

backgroundAging is accompanied by impairments in stimulus recognition, and decreased melatonin levels have been shown in aged mice and humans. These age-related changes are associated with an increased risk of neurological diseases. In the present study, our aim is to investigate whether melatonin supplementation could ameliorate age-related cognitive decline in aged mice.

methodsMice were treated with melatonin or saline. The novel object recognition (NOR) task was used to provide a simultaneous assessment of object and object location memory, which is a component of episodic-like memory. Blood-brain barrier (BBB) leakage was assessed using an Immunoglobulin G (IgG) leakage assay. Immunofluorescence and Western blot analyses were employed to investigate changes in protein levels.

resultsWe demonstrate that aging impairs memory in the NOR task, with concomitant decreases in the levels of synaptophysin (SYP), CREB-regulated transcription coactivator 1 (CRTC1), and phosphorylated AMP-activated protein kinase (p-AMPK) levels within the prefrontal cortex (PFC) and hippocampus. Moreover, alongside compromised BBB integrity, aging results in the degradation of occludin in both the PFC and hippocampus. Our findings demonstrate that aging impairs memory performance in the NOR task, accompanied by reductions in SYP, CRTC1, and p-AMPK levels within the PFC and hippocampus. Furthermore, alongside compromised BBB integrity, aging results in the degradation of occludin in both the PFC and hippocampus. More importantly, PDZ and LIM domain 5 (Pldim5) was upregulated in melatonin-treated mice, and aging-related memory impairment in the NOR task was significantly reduced in Pdlim5

conclusionsTaken together, our findings suggest that melatonin ameliorates aging-related memory decline in the NOR task by downregulating Pdlim5, maintaining BBB integrity, and upregulating CRTC1 and p-AMPK in aged mice.

Indexed as

AgingBlood-Brain BarrierMelatoninMemory DisordersMemory, EpisodicTranscription FactorsAnimalsMaleMiceMice, Inbred C57BLUp-RegulationCrtc1 protein, mouseMelatoninTranscription Factorsaged miceCRTC1episodic‐like memorymelatoninnovel object recognition

Identifiers

PMID40285336
PMCPMC12031892

What Socratic holds

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LicenceCC BY
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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 Socratic graph.