Evidence map›Paper›PMID 32860629›Full record

ArticleBritish journal of pharmacology2020

TASK-1 channel blockade by AVE1231 increases vasocontractile responses and BP in 1- to 2-week-old but not adult rats.

Anastasia A Shvetsova, Dina K Gaynullina, Nadine Schmidt, Peter Bugert, Elena V Lukoshkova, Olga S Tarasova, Rudolf Schubert

Open access · hybridAbstract read
In one paragraph

Article in British journal of pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 18 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

7 authors at 5 institutions in 3 countries.

Anastasia A ShvetsovaCentre for Biomedicine and Medical Technology Mannheim (CBTM) and European Center of Angioscience (ECAS), Research Division Cardiovascular Physiology, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.ORCID 0000-0001-8859-7689
Dina K GaynullinaFaculty of Biology, M. V. Lomonosov Moscow State University, Moscow, Russia.
Nadine SchmidtCentre for Biomedicine and Medical Technology Mannheim (CBTM) and European Center of Angioscience (ECAS), Research Division Cardiovascular Physiology, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.
Peter BugertInstitute of Transfusion Medicine and Immunology, Medical Faculty Mannheim, Heidelberg University, German Red Cross Blood Service Baden-Württemberg-Hessen, Mannheim, Germany.
Elena V LukoshkovaInstitute of Experimental Cardiology, National Medical Research Center of Cardiology, Moscow, Russia.
Olga S TarasovaFaculty of Biology, M. V. Lomonosov Moscow State University, Moscow, Russia.
Rudolf SchubertCentre for Biomedicine and Medical Technology Mannheim (CBTM) and European Center of Angioscience (ECAS), Research Division Cardiovascular Physiology, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.ORCID 0000-0003-1777-1461
Heidelberg University · DELomonosov Moscow State University · RUInstitute of Experimental Cardiology · RURussian Academy of Sciences · RUUniversity of Augsburg · DE

Funding

Deutscher Akademischer AustauschdienstRussian Science Foundation N 19-15-00210
6 · The paper itself

Abstract

background and purposeThe vasomotor role of K2P potassium channels during early postnatal development has never been investigated. We tested the hypothesis that TASK-1 channel (K2P family member) contribution to arterial vascular tone and BP is higher in the early postnatal period than in adulthood. EXPERIMENTAL APPROACH: We studied 10- to 15-day-old ("young") and 2- to 3-month-old ("adult") male rats performing digital PCR (dPCR) (using endothelium-intact saphenous arteries), isometric myography, sharp microelectrode technique, quantitative PCR (qPCR) and Western blotting (using endothelium-denuded saphenous arteries), and arterial pressure measurements under urethane anaesthesia. KEY

resultsWe found mRNA of Kcnk1-Kcnk7, Kcnk12, and Kcnk13 genes to be expressed in rat saphenous artery, and Kcnk3 (TASK-1) and Kcnk6 (TWIK-2) were most abundant in both age groups. The TASK-1 channel blocker AVE1231 (1 μmol·L CONCLUSION AND IMPLICATIONS: We showed that TASK-1 channels are important for negative feedback regulation of vasocontraction in young but not adult rats. The influence of TASK-1 channels most likely contributes to low BP level at perinatal age.

Indexed as

ArteriesMuscle, Smooth, VascularAnimalsFemaleMaleMethoxamineMyographyNerve Tissue ProteinsPotassium ChannelsPotassium Channels, Tandem Pore DomainPregnancyRatsMethoxamineNerve Tissue ProteinsPotassium ChannelsPotassium Channels, Tandem Pore Domainpotassium channel subfamily K member 3arterial smooth muscleK2Pmembrane potentialontogenesisTASK-1vascular tone

Identifiers

PMID32860629
PMCPMC7589011
OpenAlexW3082110499

What OpenQuestion holds

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LicenceCC BY
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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.