Evidence map›Paper›PMID 41417152›Full record

ArticleJournal of molecular neuroscience : MN2025

Endoplasmic Reticulum Stress Mediates Axon Initial Segment Shortening: Implications for Diabetic Brain Complications.

Jennae N Shelby, Amanda M Chisholm, Islam Akhmedov, Nathan Sheriff, Ryan B Griggs, Keiichiro Susuki

Abstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jennae N ShelbyDepartment of Neuroscience, Cell Biology, and Physiology, Boonshoft School of Medicine, Wright State University, 3640 Colonel Glenn Highway, Dayton, OH, 45435, USA.
Amanda M ChisholmDepartment of Neuroscience, Cell Biology, and Physiology, Boonshoft School of Medicine, Wright State University, 3640 Colonel Glenn Highway, Dayton, OH, 45435, USA.
Islam AkhmedovDepartment of Neuroscience, Cell Biology, and Physiology, Boonshoft School of Medicine, Wright State University, 3640 Colonel Glenn Highway, Dayton, OH, 45435, USA.
Nathan SheriffDepartment of Neuroscience, Cell Biology, and Physiology, Boonshoft School of Medicine, Wright State University, 3640 Colonel Glenn Highway, Dayton, OH, 45435, USA.
Ryan B GriggsDepartment of Neuroscience, Cell Biology, and Physiology, Boonshoft School of Medicine, Wright State University, 3640 Colonel Glenn Highway, Dayton, OH, 45435, USA.
Keiichiro SusukiDepartment of Neuroscience, Cell Biology, and Physiology, Boonshoft School of Medicine, Wright State University, 3640 Colonel Glenn Highway, Dayton, OH, 45435, USA. keiichiro.susuki@wright.edu.

Funding

ER stress mediates methylglyoxal-evoked AIS shortening and neuronal dysfunctionR01NS107398 · NINDS · WRIGHT STATE UNIVERSITY · PI SUSUKI, KEIICHIRO · 2019 to 2022
$1.4M
Unfolding the Link Between the Endoplasmic Reticulum, AIS Shortening, and Cognitive Impairment in Type 2 DiabetesF30NS124237 · NINDS · WRIGHT STATE UNIVERSITY · PI SHELBY, JENNAE NICOLLE · 2021 to 2024
$194k
NIH HHS F30 NS124237NIH HHS R01 NS107398NINDS NIH HHS F30 NS124237NINDS NIH HHS R01 NS107398
6 · The paper itself

Abstract

Endoplasmic reticulum (ER) stress and activation of the three unfolded protein response pathways, in particular the protein kinase RNA-like ER kinase (PERK) pathway, contribute to the pathophysiology of various neurodegenerative conditions including type 2 diabetes mellitus (T2DM). T2DM is an increasingly prevalent metabolic disorder affecting millions. Even with strict glucose control, patients with T2DM frequently experience mild cognitive impairment and exhibit a significantly increased risk of developing dementia. We previously demonstrated that impaired cognitive flexibility is associated with shortening of axon initial segment (AIS) length in the prefrontal cortex in the T2DM model db/db mice. The AIS plays the crucial roles of regulation of action potential initiation and neuronal output. Even subtle shortening of AIS length can reduce excitability of neurons. In this study, we hypothesized that ER stress mediates AIS shortening in diabetic conditions. Utilizing primary mouse cortical cultures, we show that sodium 4-phenylbutyrate, a well-documented ER stress inhibitor, prevents AIS shortening and PERK activation induced by the T2DM factor methylglyoxal. Exposure of cortical cultures to an established ER stress inducer tunicamycin caused dose-dependent reduction of AIS length in the generalized population of the neurons without affecting neuronal viability. Co-exposure to a PERK-specific inhibitor GSK2606414 prevented AIS shortening induced by tunicamycin. These results demonstrate ER stress is sufficient and necessary for AIS shortening in vitro. Our findings identify ER stress and AIS shortening as potential therapeutic targets in T2DM-related cognitive impairment.

Indexed as

Axon Initial SegmentDiabetes Mellitus, Type 2Endoplasmic Reticulum StressAnimalsCells, CulturedeIF-2 KinaseMiceMice, Inbred C57BLNeuronsPhenylbutyrates4-phenylbutyric acideIF-2 KinasePhenylbutyratesAxon initial segmentEndoplasmic reticulum stressMethylglyoxalProtein kinase RNA-like ER kinaseType 2 diabetes mellitus

Identifiers

PMID41417152
PMCPMC12717103

What OpenQuestion 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 OpenQuestion graph.