Phenolic Extracts from Extra Virgin Olive Oils Inhibit Dipeptidyl Peptidase IV Activity: In Vitro, Cellular, and In Silico Molecular Modeling Investigations
Carmen Lammi,
Martina Bartolomei,
Carlotta Bollati,
Lorenzo Cecchi,
Maria Bellumori,
Emanuela Sabato,
Vistoli Giulio,
Nadia Mulinacci,
Anna Arnoldi
Affiliations
Carmen Lammi
Department of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy
Martina Bartolomei
Department of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy
Carlotta Bollati
Department of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy
Lorenzo Cecchi
Department of Neuroscience, Psychology, Drug and Child Health, Pharmaceutical and Nutraceutical Section, University of Florence, 50019 Florence, Italy
Maria Bellumori
Department of Neuroscience, Psychology, Drug and Child Health, Pharmaceutical and Nutraceutical Section, University of Florence, 50019 Florence, Italy
Emanuela Sabato
Department of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy
Vistoli Giulio
Department of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy
Nadia Mulinacci
Department of Neuroscience, Psychology, Drug and Child Health, Pharmaceutical and Nutraceutical Section, University of Florence, 50019 Florence, Italy
Anna Arnoldi
Department of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy
Two extra virgin olive oil (EVOO) phenolic extracts (BUO and OMN) modulate DPP-IV activity. The in vitro DPP-IV activity assay was performed at the concentrations of 1, 10, 100, 500, and 1000 μg/mL, showing a dose-dependent inhibition by 6.8 ± 1.9, 17.4 ± 6.1, 37.9 ± 2.4, 57.8 ± 2.9, and 81 ± 1.4% for BUO and by 5.4 ± 1.7, 8.9 ± 0.4, 28.4 ± 7.2, 52 ± 1.3, and 77.5 ± 3.5% for OMN. Moreover, both BUO and OMN reduced the DPP-IV activity expressed by Caco-2 cells by 2.9 ± 0.7, 44.4 ± 0.7, 61.2 ± 1.8, and 85 ± 4.2% and by 3 ± 1.9, 35 ± 9.4, 60 ± 7.2, and 82 ± 2.8%, respectively, at the same doses. The concentration of the most abundant and representative secoiridoids within both extracts was analyzed by nuclear magnetic resonance (1H-NMR). Oleuropein, oleacein, oleocanthal, hydroxytyrosol, and tyrosol, tested alone, reduced the DPP-IV activity, with IC50 of 472.3 ± 21.7, 187 ± 11.4, 354.5 ± 12.7, 741.6 ± 35.7, and 1112 ± 55.6 µM, respectively. Finally, in silico molecular docking simulations permitted the study of the binding mode of these compounds.