Unusual Secondary Metabolites of the Aerial Parts of Dionysia diapensifolia Bioss. (Primulaceae) and Their Anti-Inflammatory Activity

• Published in: Biomolecules (Basel, Switzerland) Switzerland), 2020-03, Vol.10 (3), p.438
• Main Authors: Alilou, Mostafa, Marzocco, Stefania, Batooli, Hossein, Troppmair, Jakob, Schwaiger, Stefan, Stuppner, Hermann
• Format: Article
• Language: English
• Subjects: Animals; anti-inflammatory; Anti-Inflammatory Agents - chemistry; Anti-Inflammatory Agents - pharmacology; Cell Line; Cyclooxygenase 2 - metabolism; dionysia diapensifolia bioss; flavone; Health aspects; macrophages; Macrophages - enzymology; Macrophages - pathology; Metabolites; Mice; Nitric Oxide Synthase Type II - metabolism; phenolic compounds; Plant Components, Aerial - chemistry; Plant Extracts - chemistry; Plant Extracts - pharmacology; Primulaceae - chemistry; Secondary Metabolism
• ISSN: 2218-273X; 2218-273X
• DOI: 10.3390/biom10030438

The genus , belonging to the Primulaceae family, encompasses more than 50 species worldwide with a center of diversity located in the arid Irano-Turanian mountains. In this study, a phytochemical investigation of the aerial parts of Bioss. led to the isolation of 24 phenolic compounds - and - , and one sesquiterpenoid . Compound was identified as new natural product, while isolation of and , already known as synthetic products, from a natural source is reported for the first time in the present study. Isolation of compound from a species and indeed the whole Primulaceae family is reported for the first time too. Structure elucidation was performed by extensive spectroscopic analyses (1D-, 2D-NMR, and MS), and by comparison with reported literature data. Furthermore, DP4+ chemical shift probability calculations were performed to establish the relative configuration of compound . Additionally, subfractions obtained by liquid-liquid extraction of the methanolic extract of the plant, and subsequently the isolated new and selected known compounds - , , - obtained from the diethyl ether subfraction were investigated for their inhibitory effect on NO release and iNOS and COX-2 expression in J774A.1 murine macrophages. The results showed a potential anti-inflammatory activity of the obtained subfractions, of which the diethyl ether subfraction was the most active one in inhibiting NO release and COX-2 expression ( < 0.001). Among the investigated isolated compounds, compound significantly ( < 0.001) inhibited NO release and iNOS and COX-2 expression in a comparable manner like the used positive controls (L-NAME and indomethacin, respectively). Moreover, other isolated substances displayed moderate to high inhibitory activities, illustrating the potential anti-inflammatory activity of .