Evidence map›Paper›PMID 28797041›Full record

ArticlePloS one2017

Repeat low-level blast exposure increases transient receptor potential vanilloid 1 (TRPV1) and endothelin-1 (ET-1) expression in the trigeminal ganglion.

Elaine D Por, Melody L Sandoval, Chiquita Thomas-Benson, Teresa A Burke, Allison Doyle Brackley, Nathaniel A Jeske, Jeffery M Cleland, Brian J Lund

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. 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
0.6field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Elaine D PorOcular Trauma, United States Army Institute of Surgical Research, Fort Sam, Houston, Texas, United States of America.ORCID http://orcid.org/0000-0001-8025-5713
Melody L SandovalOcular Trauma, United States Army Institute of Surgical Research, Fort Sam, Houston, Texas, United States of America.
Chiquita Thomas-BensonOcular Trauma, United States Army Institute of Surgical Research, Fort Sam, Houston, Texas, United States of America.
Teresa A BurkeOcular Trauma, United States Army Institute of Surgical Research, Fort Sam, Houston, Texas, United States of America.
Allison Doyle BrackleyDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States of America.
Nathaniel A JeskeDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States of America.
Jeffery M ClelandOcular Trauma, United States Army Institute of Surgical Research, Fort Sam, Houston, Texas, United States of America.
Brian J LundOcular Trauma, United States Army Institute of Surgical Research, Fort Sam, Houston, Texas, United States of America.
United States Army Institute of Surgical Research · USThe University of Texas Health Science Center at San Antonio · US

Funding

A mechanism for delta opioid receptor primingF31DE025551 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI BRACKLEY, ALLISON DOYLE · 2015 to 2016
$65k
NIDCR NIH HHS F31 DE025551
6 · The paper itself

Abstract

Blast-associated sensory and cognitive trauma sustained by military service members is an area of extensively studied research. Recent studies in our laboratory have revealed that low-level blast exposure increased expression of transient receptor potential vanilloid 1 (TRPV1) and endothelin-1 (ET-1), proteins well characterized for their role in mediating pain transmission, in the cornea. Determining the functional consequences of these alterations in protein expression is critical to understanding blast-related sensory trauma. Thus, the purpose of this study was to examine TRPV1 and ET-1 expression in ocular associated sensory tissues following primary and tertiary blast. A rodent model of blast injury was used in which anesthetized animals, unrestrained or restrained, received a single or repeat blast (73.8 ± 5.5 kPa) from a compressed air shock tube once or daily for five consecutive days, respectively. Behavioral and functional analyses were conducted to assess blast effects on nocifensive behavior and TRPV1 activity. Immunohistochemistry and Western Blot were also performed with trigeminal ganglia (TG) to determine TRPV1, ET-1 and glial fibrillary associated protein (GFAP) expression following blast. Increased TRPV1, ET-1 and GFAP were detected in the TG of animals exposed to repeat blast. Increased nocifensive responses were also observed in animals exposed to repeat, tertiary blast as compared to single blast and control. Moreover, decreased TRPV1 desensitization was observed in TG neurons exposed to repeat blast. Repeat, tertiary blast resulted in increased TRPV1, ET-1 and GFAP expression in the TG, enhanced nociception and decreased TRPV1 desensitization.

Indexed as

AnimalsBlast InjuriesEndothelin-1MaleNeuronsRatsRats, Long-EvansTrigeminal GanglionTRPV Cation ChannelsEndothelin-1Trpv1 protein, ratTRPV Cation Channels

Identifiers

PMID28797041
PMCPMC5552217
OpenAlexW2744995938

What OpenQuestion holds

Textmetadata
LicenceCC0
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.