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Myrica rubra leaves as a potential source of a dual 5-LOX/COX inhibitor
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SYSNO ASEP 0474824 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Myrica 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, ORCIDNumber of authors 9 Source Title Food and Agricultural Immunology - ISSN 0954-0105
Roč. 28, č. 2 (2017), s. 343-353Number of pages 11 s. Language eng - English Country GB - United Kingdom Keywords in-vitro ; antiinflammatory activity ; zucc. leaves ; 5-lipoxygenase ; sieb. ; cyclooxygenase ; constituents ; antioxidants ; myricitrin ; metabolism ; Myrica rubra ; anti-inflammatory ; cyclooxygenase 1 ; cyclooxygenase 2 ; 5-lipoxygenase Subject RIV FR - Pharmacology ; Medidal Chemistry OECD category Medicinal chemistry R&D Projects LH12165 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) GA16-07193S GA ČR - Czech Science Foundation (CSF) Institutional support UEB-Q - RVO:61389030 UT WOS 000394647700015 DOI 10.1080/09540105.2016.1272554 Annotation Myrica 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). Workplace Institute of Experimental Botany Contact David Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469 Year of Publishing 2018
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