Tissue distribution of quercetin in pigs after long-term dietary supplementation

被引:150
作者
Bieger, Juliane [2 ]
Cermak, Rainer [1 ]
Blank, Ralf [2 ]
de Boer, Vincent C. J. [3 ]
Hollman, Peter C. H. [3 ]
Kamphues, Joseph [4 ]
Wolffram, Siegfried [2 ]
机构
[1] Univ Leipzig, Inst Vet Physiol, D-04103 Leipzig, Germany
[2] Univ Kiel, Inst Anim Nutr & Physiol, D-24098 Kiel, Germany
[3] Univ Wageningen & Res Ctr, RIKILT Inst Food Safety, NL-6708 PD Wageningen, Netherlands
[4] Univ Vet Med Hannover, Inst Anim Nutr, D-30173 Hannover, Germany
关键词
D O I
10.1093/jn/138.8.1417
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Although the flavonol quercetin is intensively investigated, our knowledge about its bioavailability and possible target organs is far from being complete. The aim of this study was to check the potential of quercetin to accumulate in various tissues after long-term dietary treatment compared with a single treatment with flavonol. Pigs ingested either a single dose of quercetin aglycone (25 mg/kg body weight; Expt. 1) or received the flavonol twice a day at the same dose mixed into their regular meals (i.e 50 mg.kg(-1).d(-1)) for 4 wk (Expt. 2). In both experiments, we took plasma and tissue samples 90 min after the final meal and analyzed them using HPLC. Additionally, the specific activity of the enzyme p-glucuronidase was measured in selected tissues. Higher flavonol concentrations than in plasma were found in only the liver (Expt. 1) or the intestinal wall and kidneys (Expt. 2). All tissues except blood plasma contained a variable amount of deconjugated quercetin in the range of 30-100% of total flavonols. However, the specific beta-glucuronidase activity was not correlated with the proportions of deconjugated flavonols in the various tissues. Long-term dietary intake of the flavonol did not lead to a greater accumulation in any tissue compared with the single treatment. Flavonol concentrations only exceeded the plasma concentration within organs involved in its metabolism and excretion, including liver, small intestine, and kidneys.
引用
收藏
页码:1417 / 1420
页数:4
相关论文
共 22 条
  • [1] Bioavailability and metabolism of the flavonol quercetin in the pig
    Ader, P
    Wessmann, A
    Wolffram, S
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (07) : 1056 - 1067
  • [2] [Anonymous], 1989, PROG NUCLEIC ACID RE
  • [3] The bioavailability of quercetin in pigs depends on the glycoside moiety and on dietary factors
    Cermak, R
    Landgraf, S
    Wolffram, S
    [J]. JOURNAL OF NUTRITION, 2003, 133 (09) : 2802 - 2807
  • [4] Part of quercetin absorbed in the small intestine is conjugated and further secreted in the intestinal lumen
    Crespy, V
    Morand, C
    Manach, C
    Besson, C
    Demigne, C
    Remesy, C
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1999, 277 (01): : G120 - G126
  • [5] Conjugation position of quercetin glucuronides and effect on biological activity
    Day, AJ
    Bao, YP
    Morgan, MRA
    Williamson, G
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (12) : 1234 - 1243
  • [6] Tissue distribution of quercetin in rats and pigs
    de Boer, VCJ
    Dihal, AA
    van der Woude, H
    Arts, ICW
    Wolffram, S
    Alink, GM
    Rietjens, IMCM
    Keijer, J
    Hollman, PCH
    [J]. JOURNAL OF NUTRITION, 2005, 135 (07) : 1718 - 1725
  • [7] Metabolic phenotype of isoflavones differ among female rats, pigs, monkeys, and women
    Gu, LW
    House, SE
    Prior, RL
    Fang, N
    Ronis, MJJ
    Clarkson, TB
    Wilson, ME
    Badger, TM
    [J]. JOURNAL OF NUTRITION, 2006, 136 (05) : 1215 - 1221
  • [8] ON THE OCCURRENCE OF FLAVONOL AND FLAVONE GLYCOSIDES IN VEGETABLES
    HERRMANN, K
    [J]. ZEITSCHRIFT FUR LEBENSMITTEL-UNTERSUCHUNG UND-FORSCHUNG, 1988, 186 (01): : 1 - 5
  • [9] DIETARY ANTIOXIDANT FLAVONOIDS AND RISK OF CORONARY HEART-DISEASE - THE ZUTPHEN ELDERLY STUDY
    HERTOG, MGL
    FESKENS, EJM
    HOLLMAN, PCH
    KATAN, MB
    KROMHOUT, D
    [J]. LANCET, 1993, 342 (8878) : 1007 - 1011
  • [10] Fluorescence detection of flavonols in HPLC by postcolumn chelation with aluminum
    Hollman, PCH
    vanTrijp, JMP
    Buysman, MNCP
    [J]. ANALYTICAL CHEMISTRY, 1996, 68 (19) : 3511 - 3515