Distribution of [ 14C]- trans-resveratrol, a cancer chemopreventive polyphenol, in mouse tissues after oral administration

Trans-resveratrol, a phenolic compound present in wine, has been reported to be a potential cancer chemopreventive agent. However, although it has numerous biological activities in vitro, there are few data about its bioavailability and tissue distribution in vivo. The objectives of this study were...

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Published in:Life sciences (1973) Vol. 72; no. 20; pp. 2219 - 2233
Main Authors: Vitrac, Xavier, Desmoulière, Alexis, Brouillaud, Brigitte, Krisa, Stéphanie, Deffieux, Gérard, Barthe, Nicole, Rosenbaum, Jean, Mérillon, Jean-Michel
Format: Journal Article
Language:English
Published: Netherlands Elsevier Inc 04.04.2003
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ISSN:0024-3205, 1879-0631
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Abstract Trans-resveratrol, a phenolic compound present in wine, has been reported to be a potential cancer chemopreventive agent. However, although it has numerous biological activities in vitro, there are few data about its bioavailability and tissue distribution in vivo. The objectives of this study were to investigate the absorption and tissue distribution of 14C- trans-resveratrol following oral administration to mice. Male Balb/c mice were given a single oral dose of 14C- trans-resveratrol and were sacrificed at 1.5, 3 or 6 h postdose. The distribution of radioactivity in tissues was evaluated using whole-body autoradiography, quantitative organ-level determination and microautoradiography. In addition, identification of radioactive compounds in kidney and liver was done with high-performance liquid chromatography. Autoradiographic survey of mice sections as well as radioactivity quantification in various organs revealed a preferential fixation of 14C- trans-resveratrol in the organs and biological liquids of absorption and elimination (stomach, liver, kidney, intestine, bile, urine). Moreover, we show that 14C- trans-resveratrol derived radioactivity is able to penetrate the tissues of liver and kidney, a finding supported by microautoradiography. The presence of intact 14C- trans-resveratrol together with glucurono- and/or sulfoconjugates in these tissues was also shown. This study demonstrates that trans-resveratrol is bioavailable following oral administration and remains mostly in intact form. The results also suggest a wide range of target organs for cancer chemoprevention by wine polyphenols in humans.
AbstractList Trans-resveratrol, a phenolic compound present in wine, has been reported to be a potential cancer chemopreventive agent. However, although it has numerous biological activities in vitro, there are few data about its bioavailability and tissue distribution in vivo. The objectives of this study were to investigate the absorption and tissue distribution of 14C- trans-resveratrol following oral administration to mice. Male Balb/c mice were given a single oral dose of 14C- trans-resveratrol and were sacrificed at 1.5, 3 or 6 h postdose. The distribution of radioactivity in tissues was evaluated using whole-body autoradiography, quantitative organ-level determination and microautoradiography. In addition, identification of radioactive compounds in kidney and liver was done with high-performance liquid chromatography. Autoradiographic survey of mice sections as well as radioactivity quantification in various organs revealed a preferential fixation of 14C- trans-resveratrol in the organs and biological liquids of absorption and elimination (stomach, liver, kidney, intestine, bile, urine). Moreover, we show that 14C- trans-resveratrol derived radioactivity is able to penetrate the tissues of liver and kidney, a finding supported by microautoradiography. The presence of intact 14C- trans-resveratrol together with glucurono- and/or sulfoconjugates in these tissues was also shown. This study demonstrates that trans-resveratrol is bioavailable following oral administration and remains mostly in intact form. The results also suggest a wide range of target organs for cancer chemoprevention by wine polyphenols in humans.
Trans-resveratrol, a phenolic compound present in wine, has been reported to be a potential cancer chemopreventive agent. However, although it has numerous biological activities in vitro, there are few data about its bioavailability and tissue distribution in vivo. The objectives of this study were to investigate the absorption and tissue distribution of 14C-trans-resveratrol following oral administration to mice. Male Balb/c mice were given a single oral dose of 14C-trans-resveratrol and were sacrificed at 1.5, 3 or 6 h postdose. The distribution of radioactivity in tissues was evaluated using whole-body autoradiography, quantitative organ-level determination and microautoradiography. In addition, identification of radioactive compounds in kidney and liver was done with high-performance liquid chromatography. Autoradiographic survey of mice sections as well as radioactivity quantification in various organs revealed a preferential fixation of 14C-trans-resveratrol in the organs and biological liquids of absorption and elimination (stomach, liver, kidney, intestine, bile, urine). Moreover, we show that 14C-trans-resveratrol derived radioactivity is able to penetrate the tissues of liver and kidney, a finding supported by microautoradiography. The presence of intact 14C-trans-resveratrol together with glucurono- and/or sulfoconjugates in these tissues was also shown. This study demonstrates that trans-resveratrol is bioavailable following oral administration and remains mostly in intact form. The results also suggest a wide range of target organs for cancer chemoprevention by wine polyphenols in humans.
Author Brouillaud, Brigitte
Rosenbaum, Jean
Barthe, Nicole
Vitrac, Xavier
Desmoulière, Alexis
Deffieux, Gérard
Krisa, Stéphanie
Mérillon, Jean-Michel
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  surname: Vitrac
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  organization: Laboratoire de Mycologie et Biotechnologie Végétale, EA 491, Université de Bordeaux 2, 146, rue Léo Saignat, 33076 Bordeaux Cedex, France
– sequence: 2
  givenname: Alexis
  surname: Desmoulière
  fullname: Desmoulière, Alexis
  organization: Groupe de Recherches pour l'Etude du Foie, INSERM, E 9917, Université de Bordeaux 2, 146, rue Léo Saignat, 33076 Bordeaux Cedex, France
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  givenname: Brigitte
  surname: Brouillaud
  fullname: Brouillaud, Brigitte
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  givenname: Stéphanie
  surname: Krisa
  fullname: Krisa, Stéphanie
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  givenname: Gérard
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  fullname: Deffieux, Gérard
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  fullname: Barthe, Nicole
  organization: Laboratoire de Biophysique, Université de Bordeaux 2, 146, rue Léo Saignat, 33076 Bordeaux Cedex, France
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  givenname: Jean
  surname: Rosenbaum
  fullname: Rosenbaum, Jean
  organization: Groupe de Recherches pour l'Etude du Foie, INSERM, E 9917, Université de Bordeaux 2, 146, rue Léo Saignat, 33076 Bordeaux Cedex, France
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  givenname: Jean-Michel
  surname: Mérillon
  fullname: Mérillon, Jean-Michel
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Keywords Red wine
Whole-body autoradiography
Bioavailability
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crossref_citationtrail_10_1016_S0024_3205_03_00096_1
elsevier_sciencedirect_doi_10_1016_S0024_3205_03_00096_1
PublicationCentury 2000
PublicationDate 2003-04-04
PublicationDateYYYYMMDD 2003-04-04
PublicationDate_xml – month: 04
  year: 2003
  text: 2003-04-04
  day: 04
PublicationDecade 2000
PublicationPlace Netherlands
PublicationPlace_xml – name: Netherlands
PublicationTitle Life sciences (1973)
PublicationTitleAlternate Life Sci
PublicationYear 2003
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
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Snippet Trans-resveratrol, a phenolic compound present in wine, has been reported to be a potential cancer chemopreventive agent. However, although it has numerous...
SourceID pubmed
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elsevier
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Enrichment Source
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StartPage 2219
SubjectTerms Administration, Oral
Animals
Anticarcinogenic Agents - administration & dosage
Anticarcinogenic Agents - pharmacokinetics
Autoradiography
Bioavailability
Biological Availability
Carbon Radioisotopes
Chromatography, High Pressure Liquid
Male
Mice
Mice, Inbred BALB C
Red wine
Resveratrol
Stilbenes - administration & dosage
Stilbenes - pharmacokinetics
Tissue Distribution
Whole-body autoradiography
Title Distribution of [ 14C]- trans-resveratrol, a cancer chemopreventive polyphenol, in mouse tissues after oral administration
URI https://dx.doi.org/10.1016/S0024-3205(03)00096-1
https://www.ncbi.nlm.nih.gov/pubmed/12628442
Volume 72
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