2003
DOI: 10.1093/ajcn/77.2.411
|View full text |Cite
|
Sign up to set email alerts
|

Comparing the pharmacokinetics of daidzein and genistein with the use of 13C-labeled tracers in premenopausal women

Abstract: The serum pharmacokinetics of [(13)C]daidzein and [(13)C]genistein were reproducible among healthy women, and genistein was more bioavailable than was daidzein. Pharmacokinetics were unaffected by chronic exposure to soy foods. Urinary isoflavone concentrations correlated poorly with maximal serum concentrations, indicating the limitations of urine measurements as a predictor of systemic bioavailability. The bioavailability of both isoflavones was nonlinear at higher intakes, suggesting that uptake is rate-lim… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

13
230
2
7

Year Published

2005
2005
2013
2013

Publication Types

Select...
5
4
1

Relationship

0
10

Authors

Journals

citations
Cited by 277 publications
(255 citation statements)
references
References 40 publications
13
230
2
7
Order By: Relevance
“…Therefore, dietary intake of isoflavones was unlikely to differ between two groups. The half-life of daidzein is relatively shorter than that of equol, and the conversion of daidzein into equol is time-dependent and slow [21]. Therefore, daidzein could be excreted rapidly in urine before its conversion into equol.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, dietary intake of isoflavones was unlikely to differ between two groups. The half-life of daidzein is relatively shorter than that of equol, and the conversion of daidzein into equol is time-dependent and slow [21]. Therefore, daidzein could be excreted rapidly in urine before its conversion into equol.…”
Section: Discussionmentioning
confidence: 99%
“…Equol is a chiral molecule capable of existing in two enantiomeric forms: R-(ϩ) equol and S-(Ϫ) equol; the latter is the natural diasteromer produced by intestinal bacteria (6,11). Both equol enantiomers show better uptake and have higher bioavailability (65-83%) than the isoflavones daidzein (30 -40%) or genistein (7-15%) (57). Both enantiomers bind ERs, with R-equol showing a preference for ER␤ (13).…”
Section: Discussionmentioning
confidence: 99%
“…Urinary concentrations of daidzein and genistein did not correlate well with the ingested doses, possibly due to limited absorption of these isoflavones at higher doses (Setchell et al, 2003a). In contrast, plasma and urine lignan concentrations after flax seed consumption increased in a dose-dependent manner (Nesbitt et al, 1999).…”
Section: Phytoestrogen Classmentioning
confidence: 93%