Evidence map›Paper›PMID 40935162›Full record

ArticleNeurobiology of disease2025

Sex differences of synaptic plasticity and microglial remodeling in the dorsal hippocampus following trigeminal nerve injury in mice.

Manindra Nath Tiwari, Lauren Paik, Fernando da Silva Fiorin, Man-Kyo Chung

Abstract read
In one paragraph

Article in Neurobiology of disease, 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

4 authors.

Manindra Nath TiwariDepartment of Neural and Pain Sciences, School of Dentistry, Center to Advance Chronic Pain Research, University of Maryland Baltimore, Baltimore, MD 21201, United States of America.
Lauren PaikDepartment of Neural and Pain Sciences, School of Dentistry, Center to Advance Chronic Pain Research, University of Maryland Baltimore, Baltimore, MD 21201, United States of America.
Fernando da Silva FiorinDepartment of Neural and Pain Sciences, School of Dentistry, Center to Advance Chronic Pain Research, University of Maryland Baltimore, Baltimore, MD 21201, United States of America.
Man-Kyo ChungDepartment of Neural and Pain Sciences, School of Dentistry, Center to Advance Chronic Pain Research, University of Maryland Baltimore, Baltimore, MD 21201, United States of America. Electronic address: MChung@umaryland.edu.

Funding

Trigeminal nociceptors: Neural intersection of chronic pain and alveolar bone remodelingR35DE030045 · NIDCR · UNIVERSITY OF MARYLAND BALTIMORE · PI Man-Kyo Chung · 2020 to 2026
$7.1M
Maryland Program in Dental Research Experience (D-REX)R25DE032530 · NIDCR · UNIVERSITY OF MARYLAND BALTIMORE · PI HENING REN · 2023 to 2026
$540k
NIDCR NIH HHS R25 DE032530NIDCR NIH HHS R35 DE030045
6 · The paper itself

Abstract

Peripheral nerve injury patients have chronic pain as well as poor memory and cognitive functioning that is associated with hippocampal abnormalities. Despite sex-dependent changes in the hippocampus of patients with chronic pain, detailed sex differences in hippocampal plasticity after peripheral nerve injury are not well known. In mice with infraorbital nerve chronic constriction injury (ION-CCI), we found complex sex differences in the dorsal hippocampus (dHC). ION-CCI suppressed population spikes amplitude and long-term potentiation (LTP) in the dHC compared to sham group, which was consistent in females but not males. The field excitatory postsynaptic potential was comparable between sexes in the sham group, and ION-CCI suppressed it in both sexes. Short-term facilitation after paired-pulse protocol was also comparable between the sexes in the sham group but was only suppressed in males with ION-CCI. While microglial numbers in the dHC were comparable between the sexes, the proportion of hyper-ramified microglia was higher in males in the sham group. ION-CCI increased the total number of microglia in both sexes; however, the proportion of hyper-ramified microglia was increased by ION-CCI in females only. In novel object recognition tests, female mice exhibited better object recognition memory than males in the sham group, which was impaired by ION-CCI. Taken together, these results suggest that female mice exhibit stronger object recognition in the uninjured condition, which may be related to stronger hippocampal synaptic functions and potentiation. Furthermore, trigeminal nerve injury may produce a greater effect on synaptic functions and plasticity, along with cognitive deficits, in females.

Indexed as

HippocampusMicrogliaNeuronal PlasticitySex CharacteristicsTrigeminal Nerve InjuriesAnimalsExcitatory Postsynaptic PotentialsFemaleLong-Term PotentiationMaleMiceMice, Inbred C57BLExcitatory post-synaptic potentialField potential, long-term potentiationMemoryMicrogliaNerve injury, hippocampus

Identifiers

PMID40935162
PMCPMC12494171

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.