Number of the records: 1  

Agonist of the adenosine A(3) receptor, IB-MECA, and inhibitor of cyclooxygenase-2, meloxicam, given alone or in a combination early after total body irradiation enhance survival of gamma-irradiated mice

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    SYSNO ASEP0427968
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleAgonist of the adenosine A(3) receptor, IB-MECA, and inhibitor of cyclooxygenase-2, meloxicam, given alone or in a combination early after total body irradiation enhance survival of gamma-irradiated mice
    Author(s) Hofer, Michal (BFU-R) RID, ORCID
    Pospíšil, Milan (BFU-R)
    Dušek, L. (CZ)
    Hoferová, Zuzana (BFU-R) RID
    Komůrková, Denisa (BFU-R) RID, ORCID
    Number of authors5
    Source TitleRadiation and Environmental Biophysics - ISSN 0301-634X
    Roč. 53, č. 1 (2014), s. 211-215
    Number of pages5 s.
    Publication formPrint - P
    Languageeng - English
    CountryDE - Germany
    KeywordsIonizing radiation ; Acute radiation disease ; Survival
    Subject RIVBO - Biophysics
    R&D ProjectsGA305/08/0158 GA ČR - Czech Science Foundation (CSF)
    GAP303/11/0128 GA ČR - Czech Science Foundation (CSF)
    Institutional supportBFU-R - RVO:68081707
    UT WOS000331977300018
    DOI10.1007/s00411-013-0500-y
    Annotationhere exists a requirement for drugs which would be useful in therapy of an acute radiation damage of a mammalian organism. The aim of the study was to evaluate survival parameters in mice exposed to a lethal gamma-ray dose of 8.5 Gy and treated with single doses of an adenosine A(3) receptor agonist, IB-MECA, or a cyclooxygenase-2 (COX-2) inhibitor, meloxicam, administered alone or in a combination early after irradiation, i.e., 0.5 and 1 h post-irradiation, respectively. The assessed parameters were the mean survival time (MST) and the cumulative percentage 30-day survival (CPS). Administrations of single intraperitoneal doses of either IB-MECA 0.5 h post-irradiation or meloxicam 1 h post-irradiation resulted in statistically significant increases of MST in comparison with the control irradiated mice. Combined administration of IB-MECA and meloxicam was found to be the only treatment statistically enhancing the parameter of CPS and to lead to the most expressive increase in MST of the experimental mice.
    WorkplaceInstitute of Biophysics
    ContactJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Year of Publishing2015
Number of the records: 1  

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