Flavonoid glycosides from Olax mannii: Structure elucidation and effect on the nuclear factor kappa B pathway

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Flavonoid glycosides from Olax mannii: Structure elucidation and effect on the nuclear factor kappa B pathway

Authors
  • B.C. Okoye, Festus
  • Richard Sawadogo, Wamtinga
  • Sendker, Jandirk
  • Aly, Amal H.
  • Quandt, Bettina
  • Wray, Victor
  • Hensel, Andreas
  • Esimone, Charles O.
  • Debbab, Abdessamad
  • Marc Diederich
  • Proksch, Peter
Type
Published Article
Journal
Journal of Ethnopharmacology
Publisher
Elsevier
Publication Date
Dec 24, 2015
Volume
176
Pages
34–34
Identifiers
DOI: 10.1016/j.jep.2015.10.019
Source
LBMCC
Funders
  • Fonds National de la Recherche Luxembourg
License
Green

Abstract

Ethnopharmacological relevance: Olax mannii Oliv. (Olacaceae) is among the many medicinal plants used in Nigeria for the ethnomedicinal management of both cancer and inflammation. Such plants represent potential sources of innovative therapeutic agents for the treatment of cancer and other malignant disorders. While the majority of medicinal plants exert their anticancer effects by direct cytotoxicity on tumor cells, it is important that other mechanisms through which these plants can exhibit anticancer effects are investigated. Preliminary studies indicated that Olax mannii leaves are rich sources of novel flavonoid glycosides. The detailed chemistry as well the mechanisms through which these flavonoid constituents may exert their cancer chemo-preventive and therapeutic effects are, however, not yet investigated. Aim of the study: The aim of this study is to carry out a detailed chemical investigation of Olax mannii leaves and the effects of the isolated constituents on the nuclear factor kappa B (NF-κB) pathway. Materials and methods: A methanol leaf extract was subjected to various chromatographic separations to achieve isolation of flavonoid glycosides and the structures of the isolated compounds were elucidated by a combination of 1D and 2D NMR and high resolution mass spectrometry. Biological activities were assessed by measurement of cellular viability and proliferation using quantitative IncuCyte videomi-croscopy, trypan blue staining and by quantification of the number of metabolically active K562 cells based on quantitation of ATP. The effect of the compounds on the inhibition of the NF-κB pathway as well as toxicity towards peripheral blood mononuclear cells to evaluate differential toxicity was also assayed.

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