Evidence map›Paper›PMID 37797902›Full record

ArticleNeurobiology of disease2023

Time- and region-dependent blood-brain barrier impairment in a rat model of organophosphate-induced status epilepticus.

Pedro N Bernardino, Brad A Hobson, Sydney L Huddleston, Peter M Andrew, Jeremy A MacMahon, Naomi H Saito, Valerie A Porter, Donald A Bruun, Danielle J Harvey, Joel R Garbow and 3 more

Open access · goldAbstract read
In one paragraph

Article in Neurobiology of disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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  10. Quantitative TNeuropharmacology · 2024
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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

13 authors at 2 institutions in 1 country.

Pedro N BernardinoDepartment of Molecular Biosciences, University of California, Davis, School of Veterinary Medicine, Davis, CA 95616, USA. Electronic address: pnberna@ucdavis.edu.
Brad A HobsonCenter for Molecular and Genomic Imaging, University of California, Davis, Davis, CA 95616, USA. Electronic address: bahobson@ucdavis.edu.
Sydney L HuddlestonCenter for Molecular and Genomic Imaging, University of California, Davis, Davis, CA 95616, USA. Electronic address: slhuddleston@ucdavis.edu.
Peter M AndrewDepartment of Molecular Biosciences, University of California, Davis, School of Veterinary Medicine, Davis, CA 95616, USA. Electronic address: pandrew@ucdavis.edu.
Jeremy A MacMahonDepartment of Molecular Biosciences, University of California, Davis, School of Veterinary Medicine, Davis, CA 95616, USA. Electronic address: jamacmahon@ucdavis.edu.
Naomi H SaitoDepartment of Public Health Sciences, University of California, Davis, School of Medicine, Davis, CA 95616, USA. Electronic address: nhsaito@ucdavis.edu.
Valerie A PorterDepartment of Biomedical Engineering, University of California, Davis, College of Engineering, Davis, CA 95616, USA. Electronic address: vporter@ucdavis.edu.
Donald A BruunDepartment of Molecular Biosciences, University of California, Davis, School of Veterinary Medicine, Davis, CA 95616, USA. Electronic address: dabruun@ucdavis.edu.
Danielle J HarveyDepartment of Public Health Sciences, University of California, Davis, School of Medicine, Davis, CA 95616, USA. Electronic address: djharvey@ucdavis.edu.
Joel R GarbowBiomedical Magnetic Resonance Center, Mallinckrodt Institute of Radiology, School of Medicine, Washington University in St. Louis, St. Louis, MO 63110, USA. Electronic address: garbow@wustl.edu.
Angie GelliDepartment of Pharmacology, University of California, Davis, School of Medicine, Davis, CA 95616, USA. Electronic address: acgelli@ucdavis.edu.
Abhijit J ChaudhariCenter for Molecular and Genomic Imaging, University of California, Davis, Davis, CA 95616, USA; Department of Radiology, University of California, Davis, School of Medicine, Sacramento, CA 95817, USA. Electronic address: ajchaudhari@ucdavis.edu.
Pamela J LeinDepartment of Molecular Biosciences, University of California, Davis, School of Veterinary Medicine, Davis, CA 95616, USA. Electronic address: pjlein@ucdavis.edu.
University of California, Davis · USMallinckrodt (United States) · US

Funding

Training and Education CoreU54NS079202 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEIN, PAMELA J · 2012 to 2021
$35.7M
UC Davis CounterACT Center of Excellence: Developing Therapeutic Strategies for Mitigating the Chronic Neurological Consequences of Acute Organophosphate IntoxicationU54NS127758 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Pamela J Lein · 2022 to 2026
$17.2M
NINDS NIH HHS U54 NS079202NINDS NIH HHS U54 NS127758
6 · The paper itself

Abstract

Acute organophosphate (OP) intoxication can trigger seizures that progress to status epilepticus (SE), and survivors often develop chronic morbidities, including spontaneous recurrent seizures (SRS). The pathogenic mechanisms underlying OP-induced SRS are unknown, but increased BBB permeability is hypothesized to be involved. Previous studies reported BBB leakage following OP-induced SE, but key information regarding time and regional distribution of BBB impairment during the epileptogenic period is missing. To address this data gap, we characterized the spatiotemporal progression of BBB impairment during the first week post-exposure in a rat model of diisopropylfluorophosphate-induced SE, using MRI and albumin immunohistochemistry. Increased BBB permeability, which was detected at 6 h and persisted up to 7 d post-exposure, was most severe and persistent in the piriform cortex and amygdala, moderate but persistent in the thalamus, and less severe and transient in the hippocampus and somatosensory cortex. The extent of BBB leakage was positively correlated with behavioral seizure severity, with the strongest association identified in the piriform cortex and amygdala. These findings provide evidence of the duration, magnitude and spatial breakdown of the BBB during the epileptogenic period following OP-induced SE and support BBB regulation as a viable therapeutic target for preventing SRS following acute OP intoxication.

Indexed as

Blood-Brain BarrierStatus EpilepticusAnimalsBrainOrganophosphatesRatsRats, Sprague-DawleySeizuresOrganophosphatesAlbuminBlood-brain barrier impairmentDiisopropylfluorophosphateEpilepsyMRIOrganophosphateSpontaneous recurrent seizures

Identifiers

PMID37797902
PMCPMC11000668
OpenAlexW4387339316

What OpenQuestion holds

Textmetadata
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.