Antioxidant and Anti-Melanogenesis Effects of Teucrium chamaedrys L. Cell Suspension Extract and Its Main Phenylethanoid Glycoside in B16-F10 Cells

Author:

Pruccoli Letizia1ORCID,Nicolini Benedetta1,Lianza Mariacaterina1ORCID,Teti Gabriella2,Falconi Mirella3,Tarozzi Andrea14ORCID,Antognoni Fabiana1ORCID

Affiliation:

1. Department for Life Quality Studies, University of Bologna, 47921 Rimini, Italy

2. Department of Biomedical and Neuromotor Sciences, University di Bologna, 40126 Bologna, Italy

3. Department of Medical and Surgical Sciences, University di Bologna, 40126 Bologna, Italy

4. Biostructures and Biosystems National Institute (INBB), 00136 Rome, Italy

Abstract

Teucrium chamaedrys L. is a typical European–Mediterranean species of the genus Teucrium. Among the phenolic compounds belonging to phenylethanoid glycosides (PGs), teucrioside (TS) is only found in this species, and it was previously demonstrated to be produced by in vitro-elicited cell cultures at levels higher than those found in leaves. However, T. chamaedrys cell suspension extracts (Cell-Ex) and pure TS have not been investigated yet for any biological effects. In this study, we evaluated the antioxidant and anti-melanogenesis activity of both Cell-Ex and TS in B16-F10 mouse melanoma cells. The results showed that Cell-Ex inhibited the reactive oxygen species formation evoked in B16-F10 cells by tert-butyl hydroperoxide and 5 J/cm2 of UVA, as well as the melanin increase stimulated by α-MSH or 20 J/cm2 of UVA. In parallel, a TS concentration equivalent to that present in Cell-Ex recorded the same biological effect profile, suggesting the main contribution of TS to the antioxidant and anti-melanogenic properties of Cell-Ex. Both Cell-Ex and TS also modulated the melanogenesis pathway through their ability to inhibit the tyrosinase activity both in a cell-free system and in B16-F10 cells stimulated by α-MSH. These results support the potential cosmeceutical use of Cell-Ex for protection against photooxidative damage and hyperpigmentation.

Publisher

MDPI AG

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