Source:http://linkedlifedata.com/resource/pubmed/id/12506986
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2002-12-31
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pubmed:abstractText |
Fluorescein is a marker-dye customary applied to the evaluation of tight-junctional permeability of epithelial cell monolayers. However, the true mechanism for the permeation has not been elucidated. Transepithelial transport of fluorescein in Caco-2 cell monolayers was therefore examined. Fluorescein transport was dependent on pH, and in a vectorical way in the apical-basolateral direction, but it was independent of the tight-junctional permeability of monolayers of these human intestinal cells. The permeation of fluorescein was concentration-dependent and saturable; the Michaelis constant was 7.7 mM and the maximum velocity was 40.3 nmol min(-1) (mg protein)(-1). Benzoic acid competitively inhibited fluorescein transport, suggesting that fluorescein is transported by a monocarboxylic acid transporter (MCT). Antioxidative polyphenolic compounds such as ferulic acid from dietary sources, competitively inhibited the permeation of fluorescein. These compounds probably share a transport carrier with fluorescein. Measurement of the effects of phenolic acids on fluorescein transport across Caco-2 monolayers would be a useful way to evaluate the intestinal absorption or bioavailability of dietary phenolic acids.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Benzoic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Coumaric Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Fluorescein,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxybenzoic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Isoquinolines,
http://linkedlifedata.com/resource/pubmed/chemical/Monocarboxylic Acid Transporters,
http://linkedlifedata.com/resource/pubmed/chemical/ferulic acid,
http://linkedlifedata.com/resource/pubmed/chemical/lucifer yellow,
http://linkedlifedata.com/resource/pubmed/chemical/phenolic acid
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0916-8451
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
66
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2449-57
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:12506986-Benzoic Acid,
pubmed-meshheading:12506986-Biological Availability,
pubmed-meshheading:12506986-Caco-2 Cells,
pubmed-meshheading:12506986-Coumaric Acids,
pubmed-meshheading:12506986-Drug Interactions,
pubmed-meshheading:12506986-Electric Impedance,
pubmed-meshheading:12506986-Epithelial Cells,
pubmed-meshheading:12506986-Fluorescein,
pubmed-meshheading:12506986-Humans,
pubmed-meshheading:12506986-Hydrogen-Ion Concentration,
pubmed-meshheading:12506986-Hydroxybenzoic Acids,
pubmed-meshheading:12506986-Intestinal Absorption,
pubmed-meshheading:12506986-Intestinal Mucosa,
pubmed-meshheading:12506986-Isoquinolines,
pubmed-meshheading:12506986-Monocarboxylic Acid Transporters,
pubmed-meshheading:12506986-Tight Junctions
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pubmed:year |
2002
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pubmed:articleTitle |
Transepithelial transport of fluorescein in Caco-2 cell monolayers and use of such transport in in vitro evaluation of phenolic acid availability.
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pubmed:affiliation |
Applied Bioresearch Center, Research & Development Dept., Kirin Brewery Co., Ltd., 3 Miyaharacho, Takasaki-shi, Gunma 370-1295, Japan. konishiy@kirin.co.jp
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pubmed:publicationType |
Journal Article
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