In vitro effects of Mangifera indica and polyphenols derived on ABCB1/P-glycoprotein activity

被引:48
|
作者
Chieli, Elisabetta [1 ]
Romiti, Nadia [1 ]
Rodeiro, Idania [2 ]
Garrido, Gabino [3 ]
机构
[1] Univ Pisa, Fac Med & Chirurg, Dipartimento Patol Sperimentale, I-56126 Pisa, Italy
[2] Ctr Quim Farmaceut, Farmacol Lab, Havana, Cuba
[3] Univ Catolica Norte, Fac Ciencias, Dept Quim & Farm, Angamos 0610, Antofagasta, Chile
关键词
Mangifera indica; Mangiferin; Norathyriol; Quercetin; P-glycoprotein; HK-2; cells; P-GLYCOPROTEIN; DRUG-INTERACTIONS; NATURAL-PRODUCTS; GRAPEFRUIT JUICE; EXTRACT VIMANG; P450; ENZYMES; CELL-LINE; QUERCETIN; CACO-2; IDENTIFICATION;
D O I
10.1016/j.fct.2009.07.017
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Many plant-derived compounds, including polyphenols, are able to affect the function of MDR-1/P-glycoprotein (P-gp ABCB1) multidrug transporter, leading to potential herb-drug interactions. This study evaluated the effects of mango (Mangifera indica L) stem bark extract, MSBE, and related phenols on P-gp activity in both the HK-2 proximal tubule cell line, constitutively expressing P-gp. and in a Caco-2 cell sub-line selected by resistance to vincristine (Caco-2/VCR) and overexpressing P-gp. The effects of MSBE, mangiferin, norathyriol, catechin, quercetin and gallic acid on P-gp activity were tested by the rhodamine-123 accumulation as well as by the Calcein-AM assays. Effects on esterase activity, which could influence the results of Calcein-AM test, were also assessed. All investigated compounds except for catechin and gallic acid inhibited P-gp activity in HK-2 cells, in the order of mangiferin < norathyriol < quercetin < MSBE. MSBE, quercetin and norathyriol also inhibited significantly esterase activity. Similar effects were obtained in resistant Caco-2/VCR cells, but were negligible in the wild-type ones, expressing low amounts of P-gp. Our results demonstrate, for the first time, that M. indica and polyphenols derived may affect the activity of the multidrug transporter P-gp ABCB1, suggesting the possibility of herb-drug interactions to be explored in depth. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2703 / 2710
页数:8
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