Evidence map›Paper›PMID 40818973›Full record

ArticleMolecular brain2025

Peripheral substance P induces deficits in hippocampal synaptic plasticity and memory.

Sun Yong Kim, Kyeong-No Yoon, Jungeun Ji, Min-Gyun Kim, Seung Ah Choi, Gunhyuk Park, Won-Woo Lee, Jin Ho Chung, Sang Jeong Kim, Joon-Yong An and 2 more

Abstract read
In one paragraph

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

0numbers the graph read from it
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

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

1 citing paper in PubMed.

  1. 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

12 authors.

Sun Yong Kim *Department of Physiology, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Kyeong-No Yoon *Department of Dermatology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, 03080, Republic of Korea.
Jungeun JiDepartment of Integrated Biomedical and Life Science, Korea University, Seoul, 02841, Republic of Korea.
Min-Gyun KimDepartment of Physiology, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Seung Ah ChoiDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Gunhyuk ParkHerbal Medicine Resources Research Center, Korea Institute of Oriental Medicine, 111 Geonjae-ro, Naju, 58245, Republic of Korea.
Won-Woo LeeDepartment of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Jin Ho ChungDepartment of Dermatology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, 03080, Republic of Korea.
Sang Jeong KimDepartment of Physiology, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea.
Joon-Yong AnDepartment of Integrated Biomedical and Life Science, Korea University, Seoul, 02841, Republic of Korea.
Dong Hun LeeDepartment of Dermatology, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, 03080, Republic of Korea. ivymed27@snu.ac.kr.
Yong-Seok LeeDepartment of Physiology, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea. yongseok7@snu.ac.kr.

Funding

Korea Health Industry Development Institute HP20C0220National Research Foundation of Korea RS-2023-NR076980
6 · The paper itself

Abstract

Substance P (SP) is a neuropeptide that functions in both the central and peripheral nervous systems. Although the peripheral actions of SP in regulating inflammatory responses have been extensively investigated, the effects of elevated peripheral SP on hippocampal functions such as spatial learning and memory remains unclear, even though SP can cross the blood-brain barrier. In this study, we found that male mice subcutaneously injected with SP for 14 days exhibited significant deficits in hippocampus-dependent memory, as assessed by the object place recognition and novel object recognition tests. In addition, long-term potentiation (LTP) at the hippocampal CA3-CA1 synapse was reduced in SP-treated mice. Transcriptomic analyses identified 77 differentially expressed genes (DEGs), and enrichment analysis highlighted pathways related to synaptic transmission, learning, and memory. These results suggest a novel skin-brain neuropeptide signaling axis. Targeting peripheral SP or its receptor may provide a therapeutic avenue for cognitive dysfunction associated with peripheral inflammation.

Indexed as

HippocampusMemoryNeuronal PlasticitySubstance PAnimalsGene Expression RegulationLong-Term PotentiationMaleMiceMice, Inbred C57BLSubstance PHippocampusLong-term potentiationSubstance PSynaptic plasticity

Identifiers

PMID40818973
PMCPMC12358064

What Socratic holds

Textmetadata
LicenceCC BY
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.