Lu Yalong, Lin Dehui, Li Wenfeng, Yang Xingbin
Shaanxi Engineering Laboratory for Food Green Processing and Safety Control, and Key Laboratory of Ministry of Education for Medicinal Resource and Natural Pharmaceutical Chemistry, College of Food Engineering and Nutritional Science, Shaanxi Normal University, Xi'an, China.
Key Laboratory of Chongqing Municipality for Protection and Utility of Unique Plant Resources in the Wulingshan Region, Life Science and Technology Institute, Yangtze Normal University, Chongqing, China.
Food Nutr Res. 2017 Aug 30;61(1):1369343. doi: 10.1080/16546628.2017.1369343. eCollection 2017.
This study was designed to explore the molecular mechanism of stachyose in enhancing the gastrointestinal stability and absorption of soybean genistein in mice. Male Kunming mice in each group (n = 8) were administered by intragastric gavage with saline, stachyose (250 mg/kg·bw), genistein (100 mg/kg·bw), and stachyose (50, 250, and 500 mg/kg·bw) together with genistein (100 mg/kg·bw) for 4 consecutive weeks, respectively, and then their urine, feces, blood, gut, and liver were collected. UPLC-qTOF/MS analysis showed that levels of genistein and its metabolites (dihydrogenistein, genistein 7-sulfate sodium salt, genistein 4'-β-D-glucuronide, and genistein 7-β-D-glucuronide) in serum and urine were increased with an increase in stachyose dosages in mice. Furthermore, the feces level of genistein aglycone was also elevated by co-treatment of stachyose with genistein. However, the feces concentration of dihydrogenistein, a characteristic metabolite of genistein by gut microorganism, was decreased by stachyose administration in a dose-dependent manner. Additionally, the simultaneous administration with stachyose and genistein in mice could decrease intestinal SULT, UGT, P-gp, and MRP1 expression, relative to the treatment with individual stachyose or genistein. These results demonstrate that stachyose-mediated inhibition against the intestinal degradation of genistein and expression of phase II enzymes and efflux transporters can largely contribute to the elevated bioavailability of soybean genistein.
本研究旨在探讨水苏糖增强小鼠胃肠道中大豆苷元稳定性及吸收的分子机制。将每组8只雄性昆明小鼠分别用生理盐水、水苏糖(250mg/kg·bw)、大豆苷元(100mg/kg·bw)以及水苏糖(50、250和500mg/kg·bw)与大豆苷元(100mg/kg·bw)连续灌胃4周,然后收集它们的尿液、粪便、血液、肠道和肝脏。超高效液相色谱-四极杆飞行时间质谱(UPLC-qTOF/MS)分析表明,随着小鼠水苏糖剂量增加,血清和尿液中大豆苷元及其代谢产物(二氢大豆苷元、大豆苷元7-硫酸钠盐、大豆苷元4'-β-D-葡萄糖醛酸苷和大豆苷元7-β-D-葡萄糖醛酸苷)水平升高。此外,水苏糖与大豆苷元共同处理也提高了粪便中大豆苷元苷元的水平。然而,水苏糖给药呈剂量依赖性降低了大豆苷元经肠道微生物作用的特征性代谢产物二氢大豆苷元的粪便浓度。另外,与单独给予水苏糖或大豆苷元相比,小鼠同时给予水苏糖和大豆苷元可降低肠道磺基转移酶(SULT)、尿苷二磷酸葡萄糖醛酸基转移酶(UGT)、P-糖蛋白(P-gp)和多药耐药相关蛋白1(MRP1)的表达。这些结果表明,水苏糖介导的对大豆苷元肠道降解以及Ⅱ相酶和外排转运体表达的抑制作用在很大程度上有助于提高大豆苷元的生物利用度。