Evidence map›Paper›PMID 26910820›Full record

ArticleMolecular neurobiology2017

Boosting Endogenous Resistance of Brain to Ischemia.

Fen Sun, Stephen R Johnson, Kunlin Jin, Victor V Uteshev

Open access · greenAbstract read
In one paragraph

Article in Molecular neurobiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 16 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

4 authors at 2 institutions in 1 country.

Fen SunInstitute for Healthy Aging, Center for Neuroscience Discovery, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX, 76107, USA.
Stephen R JohnsonCarbon Dynamics Institute, LLC, Sherman, IL, 62711, USA.
Kunlin JinInstitute for Healthy Aging, Center for Neuroscience Discovery, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX, 76107, USA.
Victor V UteshevInstitute for Healthy Aging, Center for Neuroscience Discovery, University of North Texas Health Science Center, 3500 Camp Bowie Blvd., Fort Worth, TX, 76107, USA. Victor.Uteshev@unthsc.edu.
University of North Texas · USUniversity of North Texas Health Science Center · US

Funding

Responsiveness to nicotine of nucleus tractus solitarius neuronsR01DK082625 · NIDDK · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI UTESHEV, VICTOR V · 2009 to 2013
$1.7M
NIDDK NIH HHS R01 DK082625
6 · The paper itself

Abstract

Most survivors of ischemic stroke remain physically disabled and require prolonged rehabilitation. However, some stroke victims achieve a full neurological recovery suggesting that the human brain can defend itself against ischemic injury, but the protective mechanisms are unknown. This study used selective pharmacological agents and a rat model of cerebral ischemic stroke to detect endogenous brain protective mechanisms that require activation of α7 nicotinic acetylcholine receptors (nAChRs). This endogenous protection was found to be (1) limited to less severe injuries; (2) significantly augmented by intranasal administration of a positive allosteric modulator of α7 nAChRs, significantly reducing brain injury and neurological deficits after more severe ischemic injuries; and (3) reduced by inhibition of calcium/calmodulin-dependent kinase-II. The physiological role of α7 nAChRs remains largely unknown. The therapeutic activation of α7 nAChRs after cerebral ischemia may serve as an important physiological responsibility of these ubiquitous receptors and holds a significant translational potential.

Indexed as

Administration, IntravenousAllosteric Regulationalpha7 Nicotinic Acetylcholine ReceptorAnimalsBenzenesulfonamidesBenzylaminesBrainBrain IschemiaCalcium-Calmodulin-Dependent Protein Kinase Type 2Dose-Response Relationship, DrugInfusions, IntraventricularIsoxazolesMaleOrgan Culture TechniquesPhenylurea CompoundsRats1-(5-chloro-2,4-dimethoxyphenyl)-3-(5-methylisoxazol-3-yl)ureaalpha7 Nicotinic Acetylcholine ReceptorBenzenesulfonamidesBenzylaminesCalcium-Calmodulin-Dependent Protein Kinase Type 2IsoxazolesKN 92KN 93Phenylurea CompoundsSulfonamidesAllosteric modulatorCholineNeuroprotectionNicotinic receptorsPNU-120596PNU120596Stroke

Identifiers

PMID26910820
PMCPMC4996768
OpenAlexW2285242473

What OpenQuestion holds

Textmetadata
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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.