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Myrica rubra leaves as a potential source of a dual 5-LOX/COX inhibitor

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    SYSNO ASEP0474824
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleMyrica rubra leaves as a potential source of a dual 5-LOX/COX inhibitor
    Author(s) Langhansová, Lenka (UEB-Q) RID, ORCID
    Landa, Přemysl (UEB-Q) RID, ORCID
    Kutil, Zsófia (UEB-Q)
    Tauchen, Jan (UEB-Q)
    Maršík, Petr (UEB-Q) RID, ORCID
    Rezek, Jan (UEB-Q) RID, ORCID
    Lou, J.D. (CN)
    Yun, Z.L. (CN)
    Vaněk, Tomáš (UEB-Q) RID, ORCID
    Number of authors9
    Source TitleFood and Agricultural Immunology - ISSN 0954-0105
    Roč. 28, č. 2 (2017), s. 343-353
    Number of pages11 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsin-vitro ; antiinflammatory activity ; zucc. leaves ; 5-lipoxygenase ; sieb. ; cyclooxygenase ; constituents ; antioxidants ; myricitrin ; metabolism ; Myrica rubra ; anti-inflammatory ; cyclooxygenase 1 ; cyclooxygenase 2 ; 5-lipoxygenase
    Subject RIVFR - Pharmacology ; Medidal Chemistry
    OECD categoryMedicinal chemistry
    R&D ProjectsLH12165 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    GA16-07193S GA ČR - Czech Science Foundation (CSF)
    Institutional supportUEB-Q - RVO:61389030
    UT WOS000394647700015
    DOI10.1080/09540105.2016.1272554
    AnnotationMyrica rubra Sieb. et Zucc. is a valuable fruit tree that is used in Chinese, Japanese and Taiwanese traditional medicine. We investigated the anti-inflammatory activity of M. rubra leaves extracted with four different solvents. Total phenolics were determined using the Folin-Ciocalteu method. Extracts were investigated for their inhibitory activity toward the pro-inflammatory enzymes cyclooxygenase-1 and2 (COX-1, COX-2) and 5-lipoxygenase (5-LOX). The ethanol extract of M. rubra leaves demonstrated a strong inhibition of prostaglandin E-2 (PGE(2)) biosynthesis catalyzed by both COX-1 (93.42%) and COX-2 (75.71%) and leukotriene B-4 (LTB4) formation catalyzed by 5-LOX (82.72%). Further we identified selective COX-1 inhibition by the n-butanol and aqueous fractions of the ethanol extract (with an IC50 for COX-1 inhibition of 1.07 and 0.71 mu gmL(-1) (,) respectively) and dual 5-LOX/COX inhibition by the ethyl acetate fraction (with an IC50 of 3.29 for COX-1, 2.54 for COX-2 and 8.30 mu gmL(-1) for 5-LOX).
    WorkplaceInstitute of Experimental Botany
    ContactDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Year of Publishing2018
Number of the records: 1  

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