Inhibitory effects of pomelo on the metabolism of tacrolimus and the activities of CYP3A4 and P-glycoprotein

被引:43
作者
Egashira, K [1 ]
Ohtani, H [1 ]
Itoh, S [1 ]
Koyabu, N [1 ]
Tsujimoto, M [1 ]
Murakami, H [1 ]
Sawada, Y [1 ]
机构
[1] Kyushu Univ, Grad Sch Pharmaceut Sci, Dept Medicopharmaceut Sci, Higashi Ku, Fukuoka 8128582, Japan
关键词
D O I
10.1124/dmd.32.8.828
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We recently reported a case of increase in the blood level of tacrolimus following intake of pomelo in a renal transplant recipient. To clarify the mechanism of this increase in the blood level of tacrolimus, we investigated the effect of pomelo juice extract on the activities of CYP3A4 and P-glycoprotein, in comparison with that of extract of grapefruit juice (GFJ). The 10% ethyl acetate extracts of the juice of three pomelos of different origins (Banpeiyu, pomelo I; Hirado Buntan, pomelo II; and Tosa Buntan, pomelo III) and GFJ significantly inhibited 6beta-hydroxylation of testosterone in human liver microsomes by 76.4, 67.2, 37.5, and 83.9%, respectively. The extract of pomelo I was as potent as that of GFJ. The metabolism of tacrolimus itself was also inhibited by the extract of pomelo I, as well as that of GFJ. Furthermore, the inhibition of both 6beta-hydroxylation of testosterone and metabolism of tacrolimus by pomelo I and GFJ was preincubation time-dependent. On the other hand, the extract of pomelo I had little effect on the transcellular transport of tacrolimus or [H-3] digoxin across a monolayer of LLC-GA5-COL150 cells ( a porcine kidney epithelial cell line, LLC-PK1, transfected with human MDR1 cDNA and overexpressing human P-glycoprotein). In conclusion, pomelo constituents inhibit the activity of CYP3A4 and may thereby produce an increase in the blood level of tacrolimus.
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页码:828 / 833
页数:6
相关论文
共 20 条
[1]   Effect of grapefruit juice on digoxin pharmacokinetics in humans [J].
Becquemont, L ;
Verstuyft, C ;
Kerb, R ;
Brinkmann, U ;
Lebot, M ;
Jaillon, P ;
Funck-Brentano, C .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2001, 70 (04) :311-316
[2]   Creation of polarized cells coexpressing CYP3A4, NADPH cytochrome P450 reductase and MDR1/P-glycoprotein [J].
Brimer, C ;
Dalton, JT ;
Zhu, ZX ;
Schuetz, J ;
Yasuda, K ;
Vanin, E ;
Relling, MV ;
Lu, Y ;
Schuetz, EG .
PHARMACEUTICAL RESEARCH, 2000, 17 (07) :803-810
[3]  
Edwards DJ, 1996, DRUG METAB DISPOS, V24, P1287
[4]   Pomelo-induced increase in the blood level of tacrolimus in a renal transplant patient [J].
Egashira, K ;
Fukuda, E ;
Onga, T ;
Yogi, Y ;
Matsuya, F ;
Koyabu, N ;
Ohtani, H ;
Sawada, Y .
TRANSPLANTATION, 2003, 75 (07) :1057-1057
[5]   Tacrolimus oral bioavailability doubles with coadministration of ketoconazole [J].
Floren, LC ;
Bekersky, I ;
Benet, LZ ;
Mekki, Q ;
Dressler, D ;
Lee, JW ;
Roberts, JP ;
Hebert, MF .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1997, 62 (01) :41-49
[6]  
Guo LQ, 2000, DRUG METAB DISPOS, V28, P766
[7]   Inactivation of cytochrome P450 3A4 by bergamottin, a component of grapefruit juice [J].
He, K ;
Iyer, KR ;
Hayes, RN ;
Sinz, MW ;
Woolf, TF ;
Hollenberg, PF .
CHEMICAL RESEARCH IN TOXICOLOGY, 1998, 11 (04) :252-259
[8]   Pharmacokinetic interaction of digoxin with an herbal extract from St John's wort (Hypericum perforatum) [J].
Johne, A ;
Brockmöller, J ;
Bauer, S ;
Maurer, A ;
Langheinrich, M ;
Roots, I .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1999, 66 (04) :338-345
[9]   Role of human MDR1 gene polymorphism in bioavailability and interaction of digoxin, a substrate of P-glycoprotein [J].
Kurata, Y ;
Ieiri, I ;
Kimura, M ;
Morita, T ;
Irie, S ;
Urae, A ;
Ohdo, S ;
Ohtani, H ;
Sawada, Y ;
Higuchi, S ;
Otsubo, K .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2002, 72 (02) :209-219
[10]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265