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DOI 10.3390/biom9090468

Медицинская библиотека · Biomolecules · 2019

Antioxidant Activity of Selected Stilbenoid Derivatives in a Cellular Model System.

Treml Jakub, Leláková Veronika, Šmejkal Karel, Paulíčková Tereza, Labuda Šimon, Granica Sebastian, Havlík Jaroslav, Jankovská Dagmar, Padrtová Tereza, Hošek Jan

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

The stilbenoids, a group of naturally occurring phenolic compounds, are found in a variety of plants, including some berries that are used as food or for medicinal purposes. They are known to be beneficial for human health as anti-inflammatory, chemopreventive, and antioxidative agents. We have investigated a group of 19 stilbenoid substances in vitro using a cellular model of THP-1 macrophage-like cells and pyocyanin-induced oxidative stress to evaluate their antioxidant or pro-oxidant properties. Then we have determined any effects that they might have on the expression of the enzymes catalase, glutathione peroxidase, and heme oxygenase-1, and their effects on the activation of Nrf2. The experimental results showed that these stilbenoids could affect the formation of reactive oxygen species in a cellular model, producing either an antioxidative or pro-oxidative effect, depending on the structure pinostilbene (2) worked as a pro-oxidant and also decreased expression of catalase in the cell culture. Piceatannol (4) had shown reactive oxygen species (ROS) scavenging activity, whereas isorhapontigenin (18) had a mild direct antioxidant effect and activated Nrf2-antioxidant response element (ARE) system and elevated expression of Nrf2 and catalase. Their effects shown on cells in vitro warrant their further study in vivo.

Для цитирования: Treml Jakub, Leláková Veronika, Šmejkal Karel, Paulíčková Tereza, Labuda Šimon, Granica Sebastian, Havlík Jaroslav, Jankovská Dagmar, Padrtová Tereza, Hošek Jan. Antioxidant Activity of Selected Stilbenoid Derivatives in a Cellular Model System.. Biomolecules. 2019. DOI: 10.3390/biom9090468.

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