4.7 Article

Greater Apparent Absorption of Flavonoids Is Associated with Lesser Human Fecal Flavonoid Disappearance Rates

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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 58, 期 1, 页码 141-147

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jf902284u

关键词

Flavonoid; isoflavone; bioavailability; metabolism; human

资金

  1. Center for Designing Foods to Improve Nutrition, Iowa State University
  2. U.S. Department of Agriculture Special [2003-0679]

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It was hypothesized that 5,7,4'-OH-flavonoids disappeared more rapidly from human fecal incubations and were less absorbable by humans than flavonoids without 5-OH moieties. Anaerobic fecal disappearance rates over 24 h were determined for 15 flavonoids in samples from 20 men and 13 women. In these anaerobic fecal mixtures, flavonoids with 5,7,4'-OH groups, genistein, apigenin, naringenin, luteolin, kaempferol, and quercetin (disappearance rate, k = 0.46 +/- 0.10 h(-1)), and methoxylated flavonoids, hesperetin and glycitein (k = 0.24 +/- 0.21 h(-1)), disappeared rapidly compared with flavonoids lacking 5-OH (e.g., daidzein, k = 0.07 +/- 0.03 h(-1)). Apparent absorption of flavonoids that disappeared rapidly from in vitro fecal incubations, genistein, naringenin, quercetin, and hesperetin, was compared with that of daidzein, a slowly disappearing flavonoid, in 5 men and 5 women. Subjects ingested 104 mu mol of genistein and 62 mu mol of daidzein (soy milk), 1549 mu mol of naringenin and 26 mu mol of hesperetin (grapefruit juice), and 381 mu mol of quercetin (onions) in three test meals, each separated by 1 week. Blood and urine samples were collected over 24 h after each test meal. Plasma flavonoid concentrations ranged from 0.01 to 1 mu M. The apparent absorption, expressed as percentage of ingested dose excreted in urine, was significantly less for naringenin (3.2 +/- 1.7%), genistein (7.2 +/- 4.6%), hesperetin (7.3 +/- 3.2%), and quercetin (5.6 +/- 3.7%) compared with daidzein (43.4 +/- 15.5%, p = 0.02). These data affirmed the hypothesis that the 5,7,4'-OH of flavonoids limited apparent absorption of these compounds in humans.

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