Quercetin metabolites in plasma of rats fed diets containing rutin or quercetin. 1995

C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
Laboratoire des Maladies Métaboliques, INRA de Clermont-Ferrand/Theix, St Genès-Champanelle, France.

We studied the bioavailability and the plasma transport of flavonols in rats fed quercetin or rutin diets. Wistar rats were fed one of the following purified diets for 10 d: control; 16.4 or 8.2 mmol rutin/kg diet; or 16.4, 8.2 or 4.1 mmol quercetin/kg diet. Flavonol concentrations were determined in plasma, ileal and cecal contents, and feces. In rats fed diets containing 16.4 mmol quercetin or rutin/kg, the concentration of circulating flavonols was approximately 115 mumol/L. Quercetin or rutin administration resulted in similar concentrations of quercetin in cecal contents. By HPLC analysis and beta-glucuronidase/sulfatase treatment, plasma flavonols have been identified as conjugated quercetin itself, or a conjugated form (4.5-fold as abundant) of an aglycone less polar than quercetin. Rats fed quercetin or rutin diets had a green/yellow-colored plasma that exhibited a peak absorbance at 411 nm, vs. 363 or 375 nm for pure rutin or quercetin solutions, respectively. This shift of band I absorption was obtained when pure quercetin was in the presence of albumin or added to a plasma fraction. The bathochromic properties of flavonoids in the presence of albumin are highly dependent on the presence of the C-2/C-3 double bond on the C-ring and are influenced by the degree of B-ring hydroxylation. The existence of intermolecular bonds between albumin and quercetin is supported by in vitro absorbance and fluorescence studies. With human albumin, the fluorescence intensity and the shift of quercetin absorbance increased in parallel to the albumin/quercetin molar ratio. Conjugated diene formation, resulting from Cu(2+)-catalyzed oxidation of human LDL or rat VLDL+LDL was effectively inhibited in vitro by 0.5 mumol/L quercetin. These results show that dietary flavonols are recovered in rat plasma as conjugated metabolites in non-negligible concentrations, and that these flavonols may be interesting antioxidant micronutrients with a variety of biological effects.

UI MeSH Term Description Entries
D007082 Ileum The distal and narrowest portion of the SMALL INTESTINE, between the JEJUNUM and the ILEOCECAL VALVE of the LARGE INTESTINE.
D007408 Intestinal Absorption Uptake of substances through the lining of the INTESTINES. Absorption, Intestinal
D008074 Lipoproteins Lipid-protein complexes involved in the transportation and metabolism of lipids in the body. They are spherical particles consisting of a hydrophobic core of TRIGLYCERIDES and CHOLESTEROL ESTERS surrounded by a layer of hydrophilic free CHOLESTEROL; PHOSPHOLIPIDS; and APOLIPOPROTEINS. Lipoproteins are classified by their varying buoyant density and sizes. Circulating Lipoproteins,Lipoprotein,Lipoproteins, Circulating
D008297 Male Males
D011794 Quercetin A flavonol widely distributed in plants. It is an antioxidant, like many other phenolic heterocyclic compounds. Glycosylated forms include RUTIN and quercetrin. 3,3',4',5,7-Pentahydroxyflavone,Dikvertin
D002432 Cecum The blind sac or outpouching area of the LARGE INTESTINE that is below the entrance of the SMALL INTESTINE. It has a worm-like extension, the vermiform APPENDIX. Cecums
D002851 Chromatography, High Pressure Liquid Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed. Chromatography, High Performance Liquid,Chromatography, High Speed Liquid,Chromatography, Liquid, High Pressure,HPLC,High Performance Liquid Chromatography,High-Performance Liquid Chromatography,UPLC,Ultra Performance Liquid Chromatography,Chromatography, High-Performance Liquid,High-Performance Liquid Chromatographies,Liquid Chromatography, High-Performance
D004032 Diet Regular course of eating and drinking adopted by a person or animal. Diets
D005243 Feces Excrement from the INTESTINES, containing unabsorbed solids, waste products, secretions, and BACTERIA of the DIGESTIVE SYSTEM.
D005419 Flavonoids A group of phenyl benzopyrans named for having structures like FLAVONES. 2-Phenyl-Benzopyran,2-Phenyl-Chromene,Bioflavonoid,Bioflavonoids,Flavonoid,2-Phenyl-Benzopyrans,2-Phenyl-Chromenes,2 Phenyl Benzopyran,2 Phenyl Benzopyrans,2 Phenyl Chromene,2 Phenyl Chromenes

Related Publications

C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
January 1995, Die Nahrung,
C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
January 1991, Die Nahrung,
C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
September 1992, Biological trace element research,
C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
November 2019, Journal of clinical biochemistry and nutrition,
C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
February 1998, Biochemical pharmacology,
C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
September 1988, The Journal of nutrition,
C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
September 1954, Archivio di fisiologia,
C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
August 1967, Archives of pathology,
C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
June 1991, Physiology & behavior,
C Manach, and C Morand, and O Texier, and M L Favier, and G Agullo, and C Demigné, and F Régérat, and C Rémésy
March 1996, Research in veterinary science,
Copied contents to your clipboard!