Bioguided Identification of Polymethoxyflavones as Novel Vascular CaV1.2 Channel Blockers from Citrus Peel
Authors:
- Anna RamunnoARAnna Ramunno
- Rosa Maria VitaleRVRosa Maria Vitale
- Pietro AmodeoPAPietro Amodeo
- Carlo CrescenziCarlo Crescenzi
- Alice PantiAPAlice Panti
- Paolo FiorenzaniPFPaolo Fiorenzani
- Michele De LucaMichele De Luca
- Umile Gianfranco SpizzirriUmile Gianfranco Spizzirri
- Donatella RestucciaDRDonatella Restuccia
- Francesca AielloFrancesca Aiello
- Fabio FusiFFFabio Fusi
Open Access
Abstract
The huge amount of citrus peel produced worldwide represents an economic burden for society. However, this agricultural by-product is a rich source of natural molecules, potentially endowed with interesting pharmacological activities. In this regard, we decided to investigate if the polymethoxyflavones contained in citrus peel waste could be exploited as novel vasorelaxant agents. A hydroalcoholic blond orange (Citrus sinensis) peel extract, obtained by ultrasonication, was partitioned in dichloromethane. Column chromatography allowed for the isolation of four polymethoxyflavones, namely, scutellarein tetramethyl ether, nobiletin, tangeretin, and sinensetin, identified by nuclear magnetic resonance (NMR) spectroscopy and UPLC-HRMS/MS and confirmed by multivariate curve resolution of NMR fractional spectra. The four molecules showed interesting in vitro vasorelaxant activity, at least, in part, due to the blockade of smooth muscle CaV1.2 channels. Molecular modeling and docking analysis elucidated the binding mode of the polymethoxyflavones at the homology model of the rat CaV1.2c subunit and provided the structural basis to rationalise the highest activity of scutellarein tetramethyl ether in the set and the dramatic effect of the additional methoxy group occurring in nobiletin and sinensetin. In conclusion, citrus peel can be considered a freely available, valuable source of vasoactive compounds worthy of pharmaceutical and/or nutraceutical exploitation.Keywords
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