Inhibitory effects of polyphenols on P-glycoprotein-mediated transport

被引:62
作者
Kitagawa, S [1 ]
机构
[1] Niigata Univ Pharm & Appl Life Sci, Niigata 9502081, Japan
关键词
polyphenol; flavonoid; P-glycoprotein; KB-C2; cell; multidrug resistance (MDR);
D O I
10.1248/bpb.29.1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Overexpression of P-glycoprotein (P-gp), a plasma membrane transporter which extrudes chemotherapeutic agents out of cells, has been associated with the multidrug resistance (MDR) of cancer cells. It has been revealed that flavonoids and other polyphenols inhibit P-gp activity. Due to their inhibitory activities of polyphenols on P-gp function and their physiological safety, they are possible candidates for modulators of MDR. To determine suitable candidates, it is important to clarify the structure-activity relationships of their inhibitory activities on P-gp function. Determining the structure-activity relationships is also meaningful because the intake of dietary polyphenols may also alter drug pharmacokinetics and pharmacodynamics via inhibition of P-gp-mediated drug efflux in tissues such as the intestinal epithelium, blood-brain barrier, hepatocytes and renal tubular cells. This is a review of our recent investigations using multidrug-resistant P-gp overexpressing KB-C2 cells.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 35 条
[1]   EVALUATION OF THE ANTIOXIDANT AND PROOXIDANT ACTIONS OF GALLIC ACID AND ITS DERIVATIVES [J].
ARUOMA, OI ;
MURCIA, A ;
BUTLER, J ;
HALLIWELL, B .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1993, 41 (11) :1880-1885
[2]   INHIBITION OF CA-2+-TRANSPORT ATPASE FROM SYNAPTOSOMAL VESICLES BY FLAVONOIDS [J].
BARZILAI, A ;
RAHAMIMOFF, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 730 (02) :245-254
[3]  
BATES SE, 2003, ABC PROTEINS BACTERI, P359
[4]  
BOSCH I, 1996, BIOCHIM BIOPHYS ACTA, V1288, P37
[5]   Recent advances in the discovery of flavonoids and analogs with high-affinity binding to P-glycoprotein responsible for cancer cell multidrug resistance [J].
Boumendjel, A ;
Di Pietro, A ;
Dumontet, C ;
Barron, D .
MEDICINAL RESEARCH REVIEWS, 2002, 22 (05) :512-529
[6]   Inhibition of drug transport by genistein in multidrug-resistant cells expressing P-glycoprotein [J].
Castro, AF ;
Altenberg, GA .
BIOCHEMICAL PHARMACOLOGY, 1997, 53 (01) :89-93
[7]   Biochemical mechanism of modulation of human P-glycoprotein (ABCB1) by curcumin I, II, and III purified from Turmeric powder [J].
Chearwae, W ;
Anuchapreeda, S ;
Nandigama, K ;
Ambudkar, SV ;
Limtrakul, P .
BIOCHEMICAL PHARMACOLOGY, 2004, 68 (10) :2043-2052
[8]   Flavonoids: A class of modulators with bifunctional interactions at vicinal ATP- and steroid-binding sites on mouse P-glycoprotein [J].
Conseil, G ;
Baubichon-Cortay, H ;
Dayan, G ;
Jault, JM ;
Barron, D ;
Di Pietro, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) :9831-9836
[9]  
Craig WJ, 1999, AM J CLIN NUTR, V70, p491S, DOI 10.1093/ajcn/70.3.491s
[10]   Sequence requirements of the ATP-binding site within the C-terminal nucleotide-binding domain of mouse P-glycoprotein: Structure-activity relationships for flavonoid binding [J].
de Wet, H ;
McIntosh, DB ;
Conseil, G ;
Baubichon-Cortay, H ;
Krell, T ;
Jault, JM ;
Daskiewicz, JB ;
Barron, D ;
Di Pietro, A .
BIOCHEMISTRY, 2001, 40 (34) :10382-10391