[Inhibition of advanced glycation by flavonoids. A nutritional implication for preventing diabetes complications?].

Paul Urios, Anne-Marie Grigorova-Borsos, Jacques Peyroux, Michel Sternberg
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引用次数: 8

Abstract

Advanced glycation of collagens contributes to development of micro- and macrovascular complications in diabetes. Since flavonoids are potent natural antioxidants, it was interesting to examine their effect on the formation of a cross-linking advanced glycation endproduct, pentosidine, in collagen incubated with glucose. Monomeric flavonoids (25 and 250 microM) markedly reduced pentosidine/hydroxyproline values in a concentration- and structure-dependent manner. Procyanidin oligomers from grape seed were more active than pine bark procyanidin oligomers. Oligomers are known to be cleaved into monomers in the gastric milieu and monomeric flavonoids to be absorbed and recovered at micromolar concentrations (with a long plasmatic half-life) in extracellular fluids, in contact with collagens. In conclusion, flavonoids are very potent inhibitors of pentosidine formation in collagens, active at micromolar concentrations; these concentrations might be achieved in plasma of diabetic patients after oral intake of flavonoids.

黄酮类化合物对晚期糖基化的抑制作用。预防糖尿病并发症的营养意义?
胶原的晚期糖化有助于糖尿病微血管和大血管并发症的发展。由于黄酮类化合物是有效的天然抗氧化剂,所以在与葡萄糖培养的胶原蛋白中,研究它们对交联晚期糖基化终产物戊苷形成的影响是很有趣的。单体黄酮类化合物(25和250微米)以浓度和结构依赖的方式显著降低戊苷/羟脯氨酸值。葡萄籽原花青素低聚物活性高于松皮原花青素低聚物。已知低聚物在胃环境中被分解成单体,而单体类黄酮在细胞外液中与胶原接触,以微摩尔浓度(具有较长的血浆半衰期)被吸收和回收。综上所述,黄酮类化合物是胶原中戊苷形成的有效抑制剂,在微摩尔浓度下具有活性;这些浓度可能在糖尿病患者口服黄酮类化合物后血浆中达到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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