REQUIMTE/LAQV, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, 4169-007 Porto, Portugal.
REQUIMTE/LAQV, Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, 4169-007 Porto, Portugal.
Food Chem. 2016 Feb 1;192:142-8. doi: 10.1016/j.foodchem.2015.06.108. Epub 2015 Jul 2.
The study of the antioxidant properties of six deoxyanthocyanidins (deoxypeonidin, deoxymalvidin, luteolinidin, apigeninidin, guaiacylcatechinpyrylium and syringylcatechinpyrylium) and an anthocyanin (cyanidin-3-glucoside) was carried out. The aim was to evaluate the relationship between the structure and the antioxidant properties of individual deoxyanthocyanidins, compared to a common anthocyanin derivative, cyanidin-3-glucoside. The ability of these compounds to inhibit lipid peroxidation in a liposome membrane system was examined by monitoring oxygen consumption and the antiradical and reducing capacities were determined using the DPPH and FRAP assay, respectively. The results showed that all the compounds tested presented antioxidant properties. Cyanidin-3-glucoside presented higher antiradical and reducing activities in the DPPH and FRAP assay, although in the liposome model, the guaiacylcatechinpyrylium was more effective inhibiting lipid peroxyl radicals. Additionally, the anti-proliferative effects of deoxyanthocyanidins, have been evaluated against two cancer cell lines from stomach (AGS, MKN-28) and one colon cancer cell (Caco-2), and compared with the effect of the respective anthocyanins. Considering the antiproliferative activity, all compounds were active against Caco-2 cell line, being the ones with glucose moiety and oaklin Scp the most active. Deoxyanthocyanidins, and in particular, guaiacylcatechinpyrylium may be regarded as potential food colorants.
本研究旨在评估六种去甲花色苷(去甲飞燕草素、去甲矢车菊素、木犀草素苷、芹菜素苷、愈创木基儿茶素吡喃鎓和丁香基儿茶素吡喃鎓)和一种花色苷(矢车菊素-3-葡萄糖苷)的结构与抗氧化性能之间的关系,为此,我们对这些化合物进行了研究。通过监测耗氧量,考察了这些化合物在脂质体膜系统中抑制脂质过氧化的能力,并用 DPPH 和 FRAP 测定法分别测定了它们的抗自由基和还原能力。结果表明,所有测试的化合物均具有抗氧化性能。矢车菊素-3-葡萄糖苷在 DPPH 和 FRAP 测定中表现出更高的抗自由基和还原活性,但在脂质体模型中,愈创木基儿茶素吡喃鎓抑制脂质过氧自由基的效果更显著。此外,我们还评估了去甲花色苷对两种来自胃(AGS、MKN-28)的癌细胞系和一种结肠癌细胞系(Caco-2)的抗增殖作用,并与相应花色苷的作用进行了比较。考虑到抗增殖活性,所有化合物均对 Caco-2 细胞系具有活性,其中具有葡萄糖部分和栎精 Scp 的化合物活性最强。去甲花色苷,特别是愈创木基儿茶素吡喃鎓,可被视为潜在的食品着色剂。