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DOI 10.3390/md12042228

Медицинская библиотека · Marine drugs · 2014

Maritime halophyte species from southern Portugal as sources of bioactive molecules.

Rodrigues Maria João, Gangadhar Katkam N, Vizetto-Duarte Catarina, Wubshet Sileshi G, Nyberg Nils T, Barreira Luísa, Varela João, Custódio Luísa

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Extracts of five halophytes from southern Portugal (Arthrocnemum macrostachyum, Mesembryanthemum edule, Juncus acutus, Plantago coronopus and Halimione portulacoides), were studied for antioxidant, anti-inflammatory and in vitro antitumor properties. The most active extracts towards the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical were the methanol extracts of M. edule (IC₅₀ = 0.1 mg/mL) and J. acutus (IC₅₀ = 0.4 mg/mL), and the ether extracts of J. acutus (IC₅₀ = 0.2 mg/mL) and A. macrostachyum (IC₅₀ = 0.3 mg/mL). The highest radical scavenging activity (RSA) against the 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical was obtained in the ether extract of J. acutus (IC₅₀ = 0.4 mg/mL) and H. portulacoides (IC₅₀ = 0.9 mg/mL). The maximum total phenolic content (TPC) was found in the methanol extract of M. edule (147 mg gallic acid equivalents (GAE)/g) and in the ether extract of J. acutus (94 mg GAE/g). Significant decreases in nitric oxide (NO) production were observed after incubation of macrophages with lipopolysaccharide (LPS) and the chloroform extract of H. portulacoides (IC₅₀ = 109 µg/mL) and the hexane extract of P. coronopus (IC₅₀ = 98.0 µg/mL). High in vitro cytotoxic activity and selectivity was obtained with the ether extract of J. acutus. Juncunol was identified as the active compound and for the first time was shown to display selective in vitro cytotoxicity towards various human cancer cells.

Для цитирования: Rodrigues Maria João, Gangadhar Katkam N, Vizetto-Duarte Catarina, Wubshet Sileshi G, Nyberg Nils T, Barreira Luísa, Varela João, Custódio Luísa. Maritime halophyte species from southern Portugal as sources of bioactive molecules.. Marine drugs. 2014. DOI: 10.3390/md12042228.

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