Evidence map›Paper›PMID 20531463›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2010

Adenosine can mediate its actions through generation of reactive oxygen species.

Debebe Gebremedhin, Brian Weinberger, David Lourim, David R Harder

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2010. 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
1.5field-weighted citation impact, top 18% 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, 31 citations in OpenAlex.

  1. Article
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  5. Beneficial and detrimental role of adenosine signaling in diseases and therapy.Journal of applied physiology (Bethesda, Md. : 1985) · 2015
    Review
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  12. NADPH oxidase pathway is involved in aortic contraction induced by A3 adenosine receptor in mice.The Journal of pharmacology and experimental therapeutics · 2011
    Article
  13. Review
  14. Article
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.

Debebe GebremedhinDepartment of Physiology, Medical College of Wisconsin, Milwaukee, 53226, USA. mariyei@mcw.edu
Brian Weinberger
David Lourim
David R Harder
Medical College of Wisconsin · USMilwaukee VA Medical Center · US

Funding

Role of Novel CYP Isoforms in Regulation of Cerebral Blood FlowP01HL059996 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI ROMAN, RICHARD J. · 1999 to 2009
$14.5M
REGULATING CEREBRAL MICROCIRCULATION BY ASTROCYTESR01HL033833 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HARDER, DAVID RAE · 1985 to 2017
$5.8M
Modification of Vascular Signaling in the Brain by ROSR01HL092105 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HARDER, DAVID RAE · 2009 to 2013
$2.0M
CELLULAR CONTROL MECHANISMS OF CEREBROVASCULAR TONER37HL033833 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI HARDER, DAVID R · 1990 to 1999
–
NHLBI NIH HHS HL33833-18NHLBI NIH HHS HL59996-07NHLBI NIH HHS HL9210501A1NHLBI NIH HHS R01 HL033833NHLBI NIH HHS R01 HL092105
6 · The paper itself

Abstract

Adenosine is an important cerebral vasodilator, but mediating mechanisms are not understood. We investigated the expression of adenosine receptor subtypes in isolated cerebral arterial muscle cells (CAMCs), and their role in adenosine-induced superoxide (O(2)(-)) generation and reduction in cerebral arterial tone. Reverse transcriptase-PCR, western blotting, and immunofluorescence studies have shown that CAMCs express transcript and protein for A1, A(2A), A(2B), and A(3) adenosine receptors. Stimulation of CAMCs with adenosine or the A(2A) agonist CGS-21680 increased the generation of O(2)(-) that was attenuated by the inhibition of A(2A) and A(2B) adenosine receptor subtypes, or by the peptide inhibitor of nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase gp91ds-tat, or by the mitochondria uncoupler 2,4-dinitrophenol. Application of adenosine or CGS-21680 dilated pressure-constricted cerebral arterial segments that were prevented by the antioxidants superoxide dismutase (SOD) conjugated to polyethylene glycol (PEG) and PEG-catalase or by the A(2B) adenosine receptor antagonist MRS-1754, or by the mixed A(2A) and A(2B) antagonist ZM-241385. Antagonism of the A(2A) and A(2B) adenosine receptors had no effect on cerebral vasodilatation induced by nifedipine. These findings indicate that adenosine reduces pressure-induced cerebral arterial tone through stimulation of A(2A) and A(2B) adenosine receptors and generation of O(2)(-) from NADPH oxidase and mitochondrial sources. This signaling pathway could be one of the mediators of the cerebral vasodilatory actions of adenosine.

Indexed as

VasodilationAdenosineAnimalsAntihypertensive AgentsCatalaseCells, CulturedCerebral ArteriesFree Radical ScavengersGene ExpressionMaleMuscle CellsPhenethylaminesPolyethylene GlycolsRatsRats, Sprague-DawleyReceptors, Purinergic P12-(4-(2-carboxyethyl)phenethylamino)-5'-N-ethylcarboxamidoadenosineAdenosineAntihypertensive AgentsCatalasecatalase-polyethylene glycolFree Radical ScavengersPhenethylaminesPolyethylene Glycolspolyethylene glycol-superoxide dismutaseReceptors, Purinergic P1Superoxide DismutaseSuperoxides

Identifiers

PMID20531463
PMCPMC3023402
OpenAlexW2052178798

What OpenQuestion holds

Textmetadata
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.