Evidence map›Paper›PMID 41456957›Full record

ReviewCNS neuroscience & therapeutics2025

Mitochondria-Associated Endoplasmic Reticulum Membranes as Potential Therapeutic Targets in Epilepsy.

Huaiyu Sun, Xuewei Li, Weixuan Zhao, Wuqiong Zhang, Hongmei Meng

Abstract readReview
In one paragraph

Review 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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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

5 authors.

Huaiyu SunDepartment of Neurology, The First Hospital of Jilin University, Changchun, Jilin, China.
Xuewei LiDepartment of Radiology, The First Hospital of Jilin University, Changchun, Jilin, China.
Weixuan ZhaoDepartment of Neurology, The First Hospital of Jilin University, Changchun, Jilin, China.
Wuqiong ZhangDepartment of Neurology, The First Hospital of Jilin University, Changchun, Jilin, China.ORCID 0009-0003-3136-7200
Hongmei MengDepartment of Neurology, The First Hospital of Jilin University, Changchun, Jilin, China.

Funding

Department of Science and Technology of Jilin Province 20240304165SFEducation Department of Jilin Province 2025KC102
6 · The paper itself

Abstract

backgroundMitochondria-associated endoplasmic reticulum membranes (MAMs) are specialized regions in cells where the endoplasmic reticulum and mitochondria closely interact. MAMs are enriched with a variety of proteins that regulate key cellular processes. These processes include mitochondrial fission and fusion, autophagy, lipid metabolism, calcium homeostasis, and oxidative stress. Increasing evidence suggests that disruption of MAMs structure and alterations in associated protein expression patterns are closely related to the pathogenesis of epilepsy.

methodsThis review synthesizes and analyzes current literature to outline the structural and functional roles of key MAMs proteins. It further examines experimental and clinical evidence linking MAMs dysregulation to epileptogenesis and treatment responses.

resultsThe analysis confirms that MAMs serve as a central hub coordinating cellular homeostasis. Specific alterations in MAMs structure and protein expression are consistently associated with epilepsy models. These alterations directly impact neuronal excitability, synaptic function, and cell survival pathways involved in disease progression.

conclusionAddressing these structural and functional properties of MAMs may provide valuable insights for developing novel therapeutic strategies for epilepsy.

Indexed as

Endoplasmic ReticulumEpilepsyMitochondriaAnimalsHumansendoplasmic reticulumepilepsymitochondriamitochondria‐associated endoplasmic reticulum membranestherapeutic targets

Identifiers

PMID41456957
PMCPMC12745046

What Socratic holds

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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.