Influence of Green and Black Tea on Folic Acid Pharmacokinetics in Healthy Volunteers: Potential Risk of Diminished Folic Acid Bioavailability

被引:51
作者
Alemdaroglu, N. Ceren [1 ]
Dietz, Ulrich [2 ]
Wolffram, Siegfried [3 ]
Spahn-Langguth, Hildegard [4 ]
Langguth, Peter [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Inst Pharm, D-6500 Mainz, Germany
[2] Deutsch Klin Diagnost, D-6200 Wiesbaden, Germany
[3] Univ Kiel, Inst Anim Nutr & Physiol, Kiel, Germany
[4] German Univ Cairo, Fac Pharm & Biotechnol, New Cairo City, Egypt
关键词
folic acid; green tea; black tea; pharmacokinetics; bioavailability; food-drug interaction;
D O I
10.1002/bdd.617
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Previous in vitro studies using Caco-2 cell monolayers suggested a possible interaction between green and black tea and folic acid at the level of intestinal absorption. The main purpose of the present study was to investigate a possible pharmacokinetic interaction between tea and folic acid in healthy volunteers. In an open-labeled randomized cross-over study, the pharmacokinetic interaction between tea and folic acid (0.4mg and 5mg) was investigated in healthy volunteers. Water was used as the reference drink. Subjects ingested 0.4 mg folic acid tablets with water, green or black tea (0.3 g extract/250 ml) or 5 mg folic acid tablets with water or green tea (0.3 g extract/250 ml). Blood samples were collected over a period of 8 h. Serum folate analysis was carried out by a competitive immunoassay which uses direct chemiluminescent technology. At the 0.4mg folic acid dose, green and black tea reduced the mean C-max of serum folate by 39.2% and 38.6%, and the mean AUC(0 ->) (infinity) by 26.6% and 17.9%, respectively. At the 5 mg folic acid dose, the mean C-max of serum folate was reduced by 27.4% and the mean AUC(0 ->) (infinity) was decreased significantly by 39.9% by the co-application of green tea. The present results suggest an in vivo interaction between tea and folic acid with even low concentrations of green and black tea extracts yielding decreased bioavailabilities of folic acid. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:335 / 348
页数:14
相关论文
共 71 条
[1]  
Ahn E, 2005, J POPUL THER CLIN PH, V12, pE4
[2]   Inhibition of folic acid uptake by catechins and tea extracts in Caco-2 cells [J].
Alemdaroglu, N. Ceren ;
Wolffram, Siegfried ;
Boissel, Jean-Paul ;
Closs, Ellen ;
Spahn-Langguth, Hildegard ;
Langguth, Peter .
PLANTA MEDICA, 2007, 73 (01) :27-32
[3]  
Arab L, 2000, AM J CLIN NUTR, V71, p1703S
[4]  
Arai Y, 2000, J NUTR, V130, P2243
[5]   The role of multidrug resistance efflux transporters in antifolate resistance and folate homeostasis [J].
Assaraf, Yehuda G. .
DRUG RESISTANCE UPDATES, 2006, 9 (4-5) :227-246
[6]   Loss of multidrug resistance protein 1 expression and folate efflux activity results in a highly concentrative folate transport in human leukemia cells [J].
Assaraf, YG ;
Rothem, L ;
Hooijberg, JH ;
Stark, M ;
Ifergan, I ;
Kathmann, I ;
Dijkmans, BAC ;
Peters, GJ ;
Jansen, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (09) :6680-6686
[7]   Gene and protein expression of P-glycoprotein, MRP1, MRP2, and CYP3A4 in the small and large human intestine [J].
Berggren, Sofia ;
Gall, Christine ;
Wollnitz, Nadine ;
Ekelund, Mats ;
Karlbom, Urban ;
Hoogstraate, Janet ;
Schrenk, Dieter ;
Lennernas, Hans .
MOLECULAR PHARMACEUTICS, 2007, 4 (02) :252-257
[8]   Prevention of neural-tube defects with folic acid in China [J].
Berry, RJ ;
Li, Z ;
Erickson, JD ;
Li, S ;
Moore, CA ;
Wang, H ;
Mulinare, J ;
Zhao, P ;
Wong, LYC ;
Gindler, J ;
Hong, SX ;
Correa, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (20) :1485-1490
[9]  
Brouwer IA, 2001, NUTR RES REV, V14, P267, DOI [10.1079/095442201108729240, 10.1079/NRR200126]
[10]  
BROWN JP, 1973, GASTROENTEROLOGY, V64, P223