Study on Metabolism-regulating Trace Food Factors

M. Uehara
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Abstract

Summary : Minerals, vitamins, and phytochemicals, present in trace amounts in the diet, play important roles in regulating multiple metabolic systems as well as bone metabolism. For clinical screening of phytoestrogen levels in large populations, time-resolved fluoroimmunoassay ( TR-FIA ) has been developed, and later applied for animal studies as well. Since the intestinal environment affects phytoestrogen metabolism, we investigated how a combination of prebiotics and isoflavone intake would affect isoflavone metabolism in models of osteopo-rosis. Equol, an isoflavone metabolite, contains enantiomers, and the ( S ) form is considered to exhibit higher bioavail ability than the ( R ) form, associated with a stronger inhibitory effect on bone loss in osteoporotic rodents. However, hesperidin, a citrus bioflavonoid, is thought to suppress bone loss via a cholesterol synthesis pathway different from isoflavone-related mechanisms. Sulforaphane, an anti-inflammatory sulfur-containing compound, has been considered to regulate osteoclast differentiation through suppression of osteoclast fusion molecules in addition to conventional suppression of osteoclast differentiation factors. Finally, with regard to minerals, it has been reported that lipid peroxidation is unlikely to occur in an iron-deficient state. However, in contrast to the conventional theory, we demonstrated that the in vivo oxidation mechanism was caused by iron deficiency. Furthermore, we suggested that metabolism of β -carotene and α -tocopherol was changed during iron deficiency, since it may require an iron-containing enzyme.
调节代谢的微量食物因子研究
摘要:饮食中微量的矿物质、维生素和植物化学物质在调节多种代谢系统和骨代谢中起着重要作用。时间分辨荧光免疫测定法(TR-FIA)用于临床筛选大量人群中的植物雌激素水平,后来也应用于动物研究。由于肠道环境影响植物雌激素代谢,我们研究了益生元和异黄酮摄入的组合如何影响骨质疏松模型中的异黄酮代谢。马雌酚是一种异黄酮代谢物,含有对异构体,(S)形式被认为比(R)形式具有更高的生物可利用性,对骨质疏松啮齿动物的骨质流失具有更强的抑制作用。然而,橙皮苷,柑橘类生物类黄酮,被认为通过不同于异黄酮相关机制的胆固醇合成途径抑制骨质流失。萝卜硫素是一种抗炎含硫化合物,除常规抑制破骨细胞分化因子外,还被认为通过抑制破骨细胞融合分子来调节破骨细胞分化。最后,关于矿物质,据报道,在缺铁状态下脂质过氧化不太可能发生。然而,与传统理论相反,我们证明了体内氧化机制是由缺铁引起的。此外,我们认为β -胡萝卜素和α -生育酚的代谢在缺铁时发生了变化,因为它可能需要含铁酶。
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