Evidence map›Paper›PMID 27224207›Full record

ArticleNeurotoxicology and teratology

Pharmacological blockade of the calcium plateau provides neuroprotection following organophosphate paraoxon induced status epilepticus in rats.

Laxmikant S Deshpande, Robert E Blair, Beverly A Huang, Kristin F Phillips, Robert J DeLorenzo

Open access · greenAbstract read
In one paragraph

Article in Neurotoxicology and teratology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
7.5field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  8. Review
  9. Targeting Intracellular Calcium Stores Alleviates Neurological Morbidities in a DFP-Based Rat Model of Gulf War Illness.Toxicological sciences : an official journal of the Society of Toxicology · 2019
    Article
  10. Article
  11. 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 at 1 institution in 1 country.

Laxmikant S DeshpandeDepartment of Neurology, Virginia Commonwealth University, Richmond, VA 23298, USA; Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA 23298, USA.
Robert E BlairDepartment of Neurology, Virginia Commonwealth University, Richmond, VA 23298, USA.
Beverly A HuangDepartment of Neurology, Virginia Commonwealth University, Richmond, VA 23298, USA; Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA 23298, USA.
Kristin F PhillipsDepartment of Neurology, Virginia Commonwealth University, Richmond, VA 23298, USA.
Robert J DeLorenzoDepartment of Neurology, Virginia Commonwealth University, Richmond, VA 23298, USA; Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA 23298, USA. Electronic address: Robert.DeLorenzo@vcuhealth.org.
Virginia Commonwealth University · US

Funding

PARATHION EXPOSURE: MECHANISMS OF TOXICTY AND TREATMENTU01NS058213 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI DELORENZO, ROBERT JOHN · 2006 to 2015
$5.0M
NINDS NIH HHS U01 NS058213
6 · The paper itself

Abstract

Organophosphate (OP) compounds which include nerve agents and pesticides are considered chemical threat agents. Currently approved antidotes are crucial in limiting OP mediated acute mortality. However, survivors of lethal OP exposure exhibit delayed neuronal injury and chronic behavioral morbidities. In this study, we investigated neuroprotective capabilities of dantrolene and carisbamate in a rat survival model of paraoxon (POX) induced status epilepticus (SE). Significant elevations in hippocampal calcium levels were observed 48-h post POX SE survival, and treatment with dantrolene (10mg/kg, i.m.) and carisbamate (90mg/kg, i.m.) lowered these protracted calcium elevations. POX SE induced delayed neuronal injury as characterized by Fluoro Jade C labeling was observed in critical brain areas including the dentate gyrus, parietal cortex, amygdala, and thalamus. Dantrolene and carisbamate treatment provided significant neuroprotection against delayed neuronal damage in these brain regions when administered one-hour after POX-SE. These results indicate that dantrolene or carisbamate could be effective adjuvant therapies to the existing countermeasures to reduce neuronal injury and behavioral morbidities post OP SE survival.

Indexed as

AmygdalaAnimalsAnticonvulsantsBrainCalciumCarbamatesDantroleneHippocampusMaleNeuroprotective AgentsParaoxonParietal LobeRatsRats, Sprague-DawleyStatus EpilepticusThalamusAnticonvulsantsCalciumCarbamatesDantroleneNeuroprotective AgentsParaoxonS-2-O-carbamoyl-1-o-chlorophenyl-ethanolCalciumCarisbamateCell deathDantroleneParaoxonStatus epilepticus

Identifiers

PMID27224207
PMCPMC4935577
OpenAlexW2408264969

What OpenQuestion holds

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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.