Modulation of P-glycoprotein ATPase Activity by Some Phytoconstituents

被引:81
作者
Najar, I. A. [1 ]
Sachin, B. S. [1 ]
Sharma, S. C. [1 ]
Satti, N. K. [2 ]
Suri, K. A. [2 ]
Johri, R. K. [1 ]
机构
[1] CSIR, Indian Inst Integrat Med, Div Pharmacol, Jammu 180001, India
[2] CSIR, Indian Inst Integrat Med, Div Nat Prod Chem, Jammu 180001, India
关键词
P-glycoprotein; ATPase activity; phytoconstituents; DRUG-INTERACTIONS; TRANSPORTER; INHIBITION;
D O I
10.1002/ptr.2951
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In the present investigation 16 phytoconstituents, which are active moieties round in several medicinal herbs, have been evaluated for their P-glycoprotein (P-gp) stimulation/inhibition profiles using a P-gp-dependent ATPase assay in rat jejunal membrane (in vitro). Acteoside, agnuside, catechin, chlorogenic acid, picroside -II and santonin showed an inhibitory effect. Negundoside., picroside -I and oleanolic acid caused a stimulatory effect. Andrographolide, apocyanin, berberine, glycyrrhizin, magniferin and piperine produced a biphasic response (stimulation at low concentration and inhibition at high concentration). The results suggested that a possible interaction of these phytoconstituents at the level or P-gp, could be an important parameter in determining their role in several key pharmacodynamic events. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:454 / 458
页数:5
相关论文
共 24 条
[1]   Transition state analysis of the coupling of drug transport to ATP hydrolysis by P-glycoprotein [J].
Al-Shawi, MK ;
Polar, MK ;
Omote, H ;
Figler, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (52) :52629-52640
[2]   Decrease of intestinal P-glycoprotein activity by 2n-propylquinoline, a new oral treatment for visceral leishmaniasis [J].
Belliard, AM ;
Leroy, C ;
Banide, H ;
Farinotti, R ;
Lacour, B .
EXPERIMENTAL PARASITOLOGY, 2003, 103 (1-2) :51-56
[3]   Flavonoid-mediated inhibition of intestinal ABC transporters may affect the oral bioavailability of drugs, food-borne toxic compounds and bioactive ingredients [J].
Brand, Walter ;
Schutte, Maaike E. ;
Williamson, Gary ;
van Zanden, Jelmer J. ;
Cnubben, Nicole H. P. ;
Groten, John P. ;
van Bladeren, Peter J. ;
Rietjens, Ivonne M. C. M. .
BIOMEDICINE & PHARMACOTHERAPY, 2006, 60 (09) :508-519
[4]   The effect of food components on the absorption of P-gp substrates: a review [J].
Deferme, S ;
Augustijns, P .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2003, 55 (02) :153-162
[5]   Evidence for two nonidentical drug-interaction sites in the human P-glycoprotein [J].
Dey, S ;
Ramachandra, M ;
Pastan, I ;
Gottesman, MM ;
Ambudkar, SV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (20) :10594-10599
[6]   P-glycoprotein ATPase activating effect of opioid analgesics and their P-glycoprotein-dependent antinociception in mice [J].
Hamabe, Wakako ;
Maeda, Takehiko ;
Fukazawa, Yohji ;
Kumamoto, Kazumasa ;
Shang, Lu Qing ;
Yamamoto, Akihiro ;
Yamamoto, Chizuko ;
Tokuyama, Shogo ;
Kishioka, Shiroh .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2006, 85 (03) :629-636
[7]  
He L, 2002, ACTA PHARMACOL SIN, V23, P423
[8]   IS THE MULTIDRUG TRANSPORTER A FLIPPASE [J].
HIGGINS, CF ;
GOTTESMAN, MM .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (01) :18-21
[9]  
HRYCYNA CA, 1998, METHOD ENZYMOL, V33, P456
[10]  
Ishikawa Toshihisa, 2004, Drug Metab Pharmacokinet, V19, P1, DOI 10.2133/dmpk.19.1