| Literature DB >> 27979226 |
Tuba Esatbeyoglu1, Miriam Rodríguez-Werner2, Anke Schlösser3, Peter Winterhalter2, Gerald Rimbach3.
Abstract
Sweet potato (Ipomoea batatas L.) is mainly cultivated in Asia. The deep purple color of purple sweet potato (PSP) is due to the high content of acylated anthocyanins. In the present study, PSP-derived polyphenols were identified using HPLC-PDA and HPLC-ESI-MSn analyses. After concentration of the polyphenols from PSP, preparative separation into two fractions, designated anthocyanins (AF) and copigments (CF), was carried out using adsorptive membrane chromatography. In enzyme inhibitory assays, all PSP samples inhibited the enzymes α-amylase, α-glucosidase and xanthine oxidase. Additionally, the cell signaling cellular antioxidant properties of the PSP extracts were investigated in cultured cells. PSP induced the transcription factor Nrf2, which regulates the expression of genes encoding heme oxygenase 1 (Hmox1), glutamate-cysteine ligase catalytic subunit (Gclc) and paraoxonase 1 (PON1). Furthermore, PSP enhanced cellular glutathione concentrations and decreased lipid peroxidation in cultured hepatocytes. Overall, these results suggest that PSP extracts exhibit enzyme inhibitory and cellular antioxidant properties, especially PSP CF.Entities:
Keywords: Anthocyanins; Cell culture; Chlorogenic acids; Enzyme inhibitory activity; HPLC; Membrane chromatography
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Year: 2016 PMID: 27979226 DOI: 10.1016/j.foodchem.2016.10.077
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514