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Administration of nitro-oleic acid mitigates radiation-induced hematopoietic injury in mice

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    SYSNO ASEP0564730
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleAdministration of nitro-oleic acid mitigates radiation-induced hematopoietic injury in mice
    Author(s) Perečko, Tomáš (BFU-R) RID, ORCID
    Hoferová, Zuzana (BFU-R) RID
    Hofer, Michal (BFU-R) RID, ORCID
    Perečková, Jana (BFU-R) ORCID
    Falk, Martin (BFU-R) RID, ORCID
    Number of authors5
    Article number121106
    Source TitleLife Sciences. - : Elsevier - ISSN 0024-3205
    Roč. 310, DEC 1 2022 (2022)
    Number of pages9 s.
    Publication formOnline - E
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsAcute radiation syndrome ; Bone marrow cells ; Hematopoiesis ; g-csf ; Nitrooleic acid
    Subject RIVFR - Pharmacology ; Medidal Chemistry
    OECD categoryPharmacology and pharmacy
    R&D ProjectsGA19-09212S GA ČR - Czech Science Foundation (CSF)
    Method of publishingLimited access
    Institutional supportBFU-R - RVO:68081707
    UT WOS000880317300001
    EID SCOPUS85140399032
    DOI10.1016/j.lfs.2022.121106
    AnnotationAims: Limited number of agents that provide protection against hematopoietic acute radiation syndrome led us to the evaluation of nitro-oleic acid (NO(2)OA) as a potential protector/mitigator against radiation-induced hematopoietic injury in C57/BL6 mice. Materials and methods: NO(2)OA was administered before and after sub-lethal total body irradiation (TBI) and hematological parameters were evaluated 3 or 7 days after TBI. Key findings: Our results show that NO(2)OA significantly increase bone marrow cellularity including the granulocyte-macrophage colony-forming cells and erythroid progenitors on the 3rd day after TBI. In addition, NO(2)OA enhanced recovery of white blood cells (lymphocytes, neutrophils, and monocytes) in peripheral blood 7 days after irradiation. These effects may be in part attributed to NO(2)OA-induced granulocyte colony-stimulating factor production after TBI. On the other hand, radiation-induced impairment of peripheral red blood cells, hemoglobin, and platelets were not affected with NO(2)OA treatment up to 7 days post TBI. Significance: In conclusion, our data show that NO(2)OA significantly protects hematopoiesis after irradiation, and thus showed a high potential to act as an agent for medical radiation countermeasure.
    WorkplaceInstitute of Biophysics
    ContactJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Year of Publishing2023
    Electronic addresshttps://www.sciencedirect.com/science/article/pii/S0024320522008062?via%3Dihub
Number of the records: 1  

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