The intestinal absorption of isoflavones is an essential prerequisite for assuring biologic effects. The purpose of this study was to investigate the intestinal transport, metabolism, and tissue uptake of daidzein. To this aim, 3 different tracts of small intestine of rats (proximal, medial, and distal) were isolated, everted, and exposed to physiologic concentrations (mucosal side) of daidzein (25, 50, and 80 (mu)mol/L); perfusion experiments were performed for 60 minutes. Concentrations of total daidzein (at 30, 45, and 60 minutes) and glucuronide daidzein (at 60 minutes) were analyzed on aliquots of serosal solutions, whereas whole intestinal tracts were analyzed to determine daidzein tissue uptake (at 60 minutes). Results show linear relationships between the amounts of aglycone absorbed and taken up by tissue and mucosal daidzein concentrations; both amounts were higher in the distal tracts than in the other intestinal tracts (P < .05). The extrapolated total daidzein intestinal absorption was about 6% and total tissue uptake was about 10%. The amounts of conjugate daidzein correspond on average to about 6% of the levels absorbed; results suggest an inverse correlation between conjugation activity and mucosal daidzein concentration. In conclusion, our study suggests that a passive, unsaturable transport is the only mechanism of daidzein absorption in the small intestine of rats, at least within the concentrations tested. Different daidzein permeability of rat intestinal tracts was also demonstrated. (copyright) 2006 Elsevier Inc. All rights reserved.

Daidzein is absorbed by passive transport in isolated small intestine of rats / P. Foti, D. Erba, A. Spadafranca, S. Ciappellano, J. Bresciani, G. Testolin. - In: NUTRITION RESEARCH. - ISSN 0271-5317. - 26:6(2006), pp. 284-288. [10.1016/j.nutres.2006.06.005]

Daidzein is absorbed by passive transport in isolated small intestine of rats

P. Foti
Primo
;
D. Erba
Secondo
;
A. Spadafranca;S. Ciappellano;J. Bresciani
Penultimo
;
G. Testolin
Ultimo
2006

Abstract

The intestinal absorption of isoflavones is an essential prerequisite for assuring biologic effects. The purpose of this study was to investigate the intestinal transport, metabolism, and tissue uptake of daidzein. To this aim, 3 different tracts of small intestine of rats (proximal, medial, and distal) were isolated, everted, and exposed to physiologic concentrations (mucosal side) of daidzein (25, 50, and 80 (mu)mol/L); perfusion experiments were performed for 60 minutes. Concentrations of total daidzein (at 30, 45, and 60 minutes) and glucuronide daidzein (at 60 minutes) were analyzed on aliquots of serosal solutions, whereas whole intestinal tracts were analyzed to determine daidzein tissue uptake (at 60 minutes). Results show linear relationships between the amounts of aglycone absorbed and taken up by tissue and mucosal daidzein concentrations; both amounts were higher in the distal tracts than in the other intestinal tracts (P < .05). The extrapolated total daidzein intestinal absorption was about 6% and total tissue uptake was about 10%. The amounts of conjugate daidzein correspond on average to about 6% of the levels absorbed; results suggest an inverse correlation between conjugation activity and mucosal daidzein concentration. In conclusion, our study suggests that a passive, unsaturable transport is the only mechanism of daidzein absorption in the small intestine of rats, at least within the concentrations tested. Different daidzein permeability of rat intestinal tracts was also demonstrated. (copyright) 2006 Elsevier Inc. All rights reserved.
Daidzein; Everted gut; Intestinal absorption; Intestinal metabolism; Rats
Settore BIO/09 - Fisiologia
2006
Article (author)
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/23543
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 8
  • ???jsp.display-item.citation.isi??? 8
social impact