Evidence map›Paper›PMID 23288107›Full record

ArticleJournal of cardiovascular pharmacology2013

Functional and RNA expression profile of adenosine receptor subtypes in mouse mesenteric arteries.

Bunyen Teng, Daniel Fil, Stephen L Tilley, Catherine Ledent, Thomas Krahn, S Jamal Mustafa

Open access · greenAbstract read
In one paragraph

Article in Journal of cardiovascular pharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 27 citations in OpenAlex.

  1. APurinergic signalling · 2025
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  7. Aldosterone impairs coronary adenosine-mediated vasodilation via reduced functional expression of CaAmerican journal of physiology. Heart and circulatory physiology · 2019
    Article
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  9. Enhanced AEuropean journal of pharmacology · 2019
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  15. Role of Adenosine Receptor(s) in the Control of Vascular Tone in the Mouse Pudendal Artery.The Journal of pharmacology and experimental therapeutics · 2016
    Article
  16. Article
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  19. Metabolic hyperemia requires ATP-sensitive K+ channels and H2O2 but not adenosine in isolated mouse hearts.American journal of physiology. Heart and circulatory physiology · 2014
    Article
  20. 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

6 authors at 4 institutions in 3 countries.

Bunyen TengDepartment of Physiology and Pharmacology, Center for Cardiovascular and Respiratory Sciences, West Virginia University, Morgantown, WV 26506, USA. bteng@hsc.wvu.edu
Daniel Fil
Stephen L Tilley
Catherine Ledent
Thomas Krahn
S Jamal Mustafa
West Virginia University · USBayer (Germany) · DEPulmonary Associates · USUniversité Libre de Bruxelles · BE

Funding

MECHANISMS OF CORONARY FLOW REGULATION BY ADENOSINER01HL027339 · NHLBI · WEST VIRGINIA UNIVERSITY · PI MUSTAFA, S. JAMAL · 1986 to 2015
$5.0M
Role of CYP P450s in the Regulation of Vascular Tone through Adenosine ReceptorsR01HL094447 · NHLBI · WEST VIRGINIA UNIVERSITY · PI MUSTAFA, S. JAMAL · 2009 to 2013
$2.4M
NHLBI NIH HHS AND HL 027339NHLBI NIH HHS HL 094447NHLBI NIH HHS R01 HL027339NHLBI NIH HHS R01 HL094447
6 · The paper itself

Abstract

Concentration-response curves (CRCs) of adenosine receptor (AR) agonists, NECA (nonspecific), CCPA (A1 specific), CGS-216870 (A2A specific), BAY 60-6583 (A2B specific), and Cl-IB-MECA (A3 specific) for mesenteric arteries (MAs) from 4 AR knockout (KO) mice (A1, A2A, A2B, and A3) and their wild type (WT) were constructed. The messenger RNA expression of MAs from KO mice and WT were also studied. Adenosine (10 to 10 M) and NECA (10 to 10 M) induced relaxation in all mice except A2B KO mice, which only showed constriction by adenosine at 10 to 10 and NECA at 10 to 10 M. The CCPA induced a significant constriction at 10 and 10 M in all mice, except A1KO. BAY 60-6583 induced relaxation (10 to 10 M) in WT and no response in A2BKO except at 10 M. The CRCs for BAY 60-6583 in A1, A2A, and A3 KO mice shifted to the left when compared with WT mice, suggesting an upregulation of A2B AR. No responses were noted to CGS-21680 in all mice. Cl-IB-MECA only induced relaxation at concentration greater than 10 M, and no differences were found between different KO mice. The CRC for Bay 60-6583 was not significantly changed in the presence of 10 M of L-NAME, 10 M of indomethacin, or both. Our data suggest that A2B AR is the predominant AR subtype and the effect may be endothelial independent, whereas A1 AR plays a significant modulatory role in mouse MAs.

Indexed as

AnimalsDose-Response Relationship, DrugGene Expression RegulationMesenteric ArteriesMiceMice, Inbred C57BLMice, KnockoutPurinergic P1 Receptor AgonistsReceptor, Adenosine A1Receptor, Adenosine A2AReceptor, Adenosine A2BReceptor, Adenosine A3Receptors, Purinergic P1RNA, MessengerVasoconstrictionVasodilationPurinergic P1 Receptor AgonistsReceptor, Adenosine A1Receptor, Adenosine A2AReceptor, Adenosine A2BReceptor, Adenosine A3Receptors, Purinergic P1RNA, Messenger

Identifiers

PMID23288107
PMCPMC3539216
OpenAlexW2042904632

What OpenQuestion holds

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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.