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Anti-inflammatory effect of Adelia ricinella L. aerial parts
Author(s) -
Clara Azalea Berenguer-Rivas,
Julio César Escalona Arranz,
Gabriel Llauradó Maury,
Anastasia Van der Auwera,
Stefano Piazza,
Daniel Méndez,
Kenn Foubert,
Paul Cos,
Luc Pieters
Publication year - 2021
Publication title -
journal of pharmacy and pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 118
eISSN - 2042-7158
pISSN - 0022-3573
DOI - 10.1093/jpp/rgaa057
Subject(s) - apigenin , luteolin , chemistry , phytochemical , viability assay , western blot , anti inflammatory , in vitro , traditional medicine , enzyme , ethanol , cell culture , biochemistry , chromatography , pharmacology , flavonoid , biology , medicine , antioxidant , genetics , gene
Objective To investigate the main chemical components and the anti-inflammatory activity of extracts of Adelia ricinella L. aerial parts. Methods Three extracts obtained by soxhlet extraction and ethanol/water mixtures were evaluated in their chemical composition by UPLC-DAD-MS/MS. The in vitro anti-inflammatory activity of the prepared extracts was assessed through three different assays: COX-1 and COX-2 enzymatic inhibition, cell-based COX assays on RAW264.7 macrophages (ATCC) measuring the COX-2 protein expression by Western blot and the measurement of the PGE2 concentration in the supernatants of the culture medium. Also was determinate the effect of the three extracts on the RAW 264.7 cell viability. Key findings Few differences in the phytochemical profile were found between the three prepared extracts, identifying a blend of thirteen flavonoids derived from luteolin and apigenin, with orientin as main constituent. Plant extracts (alcoholic and aqueous) did not affect the macrophage cell viability (IC50 > 256 μg/ml) and significantly reduced COX-1 and COX-2 enzyme activities. Additionally, COX-2 expression and PGE2 release were suppressed after 24 h of LPS stimulation and treatment with plant extracts (8–64 µg/ml). Conclusions A. ricinella extracts showed the ability to reduce the inflammatory effect exerted by LPS in murine macrophages. However, further studies should confirm their anti-inflammatory activity.

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