Evidence map›Paper›PMID 34580742›Full record

ArticleCellular and molecular life sciences : CMLS2021

A cellular approach to understanding and treating Gulf War Illness.

Philip L Yates, Ankita Patil, Xiaohuan Sun, Alessia Niceforo, Ramnik Gill, Patrick Callahan, Wayne Beck, Emanuela Piermarini, Alvin V Terry, Kimberly A Sullivan and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 15% of its field
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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  5. Review
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  7. Article
  8. Is Gulf War Illness a prolonged early phase tauopathy?Cytoskeleton (Hoboken, N.J.) · 2024
    Article
  9. Review
  10. Observational
  11. Article
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  14. 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

12 authors at 3 institutions in 1 country.

Philip L YatesDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA, 19129, USA.
Ankita PatilDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA, 19129, USA.
Xiaohuan SunDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA, 19129, USA.
Alessia NiceforoDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA, 19129, USA.
Ramnik GillDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA, 19129, USA.
Patrick CallahanDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.
Wayne BeckDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.
Emanuela PiermariniDepartment of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA, 19129, USA.
Alvin V TerryDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.
Kimberly A SullivanDepartment of Environmental Health, Boston University School of Public Health, Boston, MA, 02118, USA.
Peter W Baas *Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA, 19129, USA.
Liang Qiang *Department of Neurobiology and Anatomy, Drexel University College of Medicine, 2900 Queen Lane, Philadelphia, PA, 19129, USA. lq24@drexel.edu.ORCID http://orcid.org/0000-0001-9896-602X
Drexel University · USAugusta University · USBoston University · US

Funding

MICROTUBULE DYNAMICS AND AXON GROWTHR01NS028785 · NINDS · UNIVERSITY OF WISCONSIN MADISON · PI BAAS, PETER W. · 1990 to 2021
$7.3M
Interdisciplinary And Translational Research Training In NeurohivT32MH079785 · NIMH · TEMPLE UNIV OF THE COMMONWEALTH · PI Kamel Khalili · 2008 to 2026
$5.4M
Elucidating the etiology of SPAST-based Hereditary Spastic ParaplegiaR01NS115977 · NINDS · DREXEL UNIVERSITY · PI QIANG, LIANG · 2021 to 2025
$1.8M
Role of Tau in Microtubule Stability in Adult NeuronsR21AG068597 · NIA · DREXEL UNIVERSITY · PI BAAS, PETER W. · 2021 to 2021
$416k
Using multiple species, stimuli, and tasks to study the neural basis of visually guided behaviorK99NS118117 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NI, AMY MEESUN · 2020 to 2021
$239k
foundation for the national institutes of health 1R01NS115977foundation for the national institutes of health R01NS118117foundation for the national institutes of health R01NS28785foundation for the national institutes of health R21AG068597foundation for the national institutes of health T32-MH079785NIA NIH HHS R21 AG068597NIMH NIH HHS T32 MH079785NINDS NIH HHS K99 NS118117NINDS NIH HHS R01 NS028785NINDS NIH HHS R01 NS115977u.s. department of defense GW160151u.s. department of defense GW170023u.s. department of defense GW170055
6 · The paper itself

Abstract

Gulf War Illness (GWI), a disorder suffered by approximately 200,000 veterans of the first Gulf War, was caused by exposure to low-level organophosphate pesticides and nerve agents in combination with battlefield stress. To elucidate the mechanistic basis of the brain-related symptoms of GWI, human-induced pluripotent stem cells (hiPSCs) derived from veterans with or without GWI were differentiated into forebrain glutamatergic neurons and then exposed to a Gulf War (GW) relevant toxicant regimen consisting of a sarin analog and cortisol, a human stress hormone. Elevated levels of total and phosphorylated tau, reduced microtubule acetylation, altered mitochondrial dynamics/transport, and decreased neuronal activity were observed in neurons exposed to the toxicant regimen. Some of the data are consistent with the possibility that some veterans may have been predisposed to acquire GWI. Wistar rats exposed to a similar toxicant regimen showed a mild learning and memory deficit, as well as cell loss and tau pathology selectively in the CA3 region of the hippocampus. These cellular responses offer a mechanistic explanation for the memory loss suffered by veterans with GWI and provide a cell-based model for screening drugs and developing personalized therapies for these veterans.

Indexed as

AnimalsCA3 Region, HippocampalCell DifferentiationCells, CulturedDisease Models, AnimalGulf WarHumansInduced Pluripotent Stem CellsMaleMemory DisordersNeuronsPersian Gulf SyndromeRatsRats, WistarVeteransGulf War IllnessHuman-induced pluripotent stem cellsMemoryMicrotubuleMitochondriaNeuronal activityTau

Identifiers

PMID34580742
PMCPMC9669894
OpenAlexW3203155006

What OpenQuestion holds

Textmetadata
LicenceTDM
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.