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Metabolite Profile and Antiproliferative Effects in HaCaT Cells of a Salix reticulata Extract.
Corradi, Elisabetta; Schmidt, Nadine; Räber, Nathalie; De Mieri, Maria; Hamburger, Matthias; Butterweck, Veronika; Potterat, Olivier.
Afiliação
  • Corradi E; Division of Pharmaceutical Biology, University of Basel, Switzerland.
  • Schmidt N; Institute for Pharma Technology, School of Life Sciences, University of Applied Sciences Northwestern Switzerland, Muttenz, Switzerland.
  • Räber N; Division of Pharmaceutical Biology, University of Basel, Switzerland.
  • De Mieri M; Division of Pharmaceutical Biology, University of Basel, Switzerland.
  • Hamburger M; Division of Pharmaceutical Biology, University of Basel, Switzerland.
  • Butterweck V; Institute for Pharma Technology, School of Life Sciences, University of Applied Sciences Northwestern Switzerland, Muttenz, Switzerland.
  • Potterat O; Division of Pharmaceutical Biology, University of Basel, Switzerland.
Planta Med ; 83(14-15): 1149-1158, 2017 Oct.
Article em En | MEDLINE | ID: mdl-28449181
ABSTRACT
Phenolic constituents of Salix reticulata (Salicaceae) and antiproliferative activity of an extract and individual compounds were investigated in immortalized human non-tumorigenic keratinocytes (HaCaT). A MeOH extract from aerial parts afforded several flavonoids, including luteolin and apigenin glycosides (2-5 and 9) and catechin (1), two procyanidin fractions, and the phenolic glucosides picein (6), triandrin (7), and salicortin (8). In an adenosine triphosphate assay, the MeOH extract reduced cell viability by approximately 60 % at a concentration of 100 µg/mL. Cell proliferation was assessed with a BrdU incorporation ELISA assay. The extract inhibited proliferation of HaCaT cells in a concentration-dependent manner, with approximately 50 % inhibition at 100 µg/mL. In time-lapse assays, the extract showed distinct inhibitory effects on cell migration at concentrations of 12.5, 25, and 50 µg/mL. The activity of selected constituents was also determined. Luteolin-7-O-ß-glucuronide (3) significantly inhibited cell proliferation at concentrations of 10 and 50 µM. In contrast, luteolin-7-O-ß-glucopyranoside (2) and a procyanidin fraction (P1) had only weak effects, while picein (6) and salicortin (8) did not affect cell proliferation. Luteolin-7-O-ß-glucuronide (10 µM) and, to a lesser extent, the procyanidin fraction (10 µg/mL) also inhibited cell migration.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenóis / Extratos Vegetais / Salix / Glicosídeos Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenóis / Extratos Vegetais / Salix / Glicosídeos Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article