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Published in: Clinical Pharmacokinetics 3/2001

01-03-2001 | Leading Article

The Gut as a Barrier to Drug Absorption

Combined Role of Cytochrome P450 3A and P-Glycoprotein

Authors: Dr Yuanchao Zhang, Leslie Z. Benet

Published in: Clinical Pharmacokinetics | Issue 3/2001

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Abstract

Intestinal phase I metabolism and active extrusion of absorbed drug have recently been recognised as major determinants of oral bioavailability. Cytochrome P450 (CYP) 3A, the major phase I drug metabolising enzyme in humans, and the multidrug efflux pump, P-glycoprotein, are present at high levels in the villus tip of enterocytes in the gastrointestinal tract, the primary site of absorption for orally administered drugs. The importance of CYP3A and P-glycoprotein in limiting oral drug delivery is suggested to us by their joint presence in small intestinal enterocytes, by the significant overlap in their substrate specificities, and by the poor oral bioavailability of joint substrates for these 2 proteins. These proteins are induced or inhibited by many of the same compounds.
A growing number of preclinical and clinical studies have demonstrated that the oral bioavailability of many CYP3A and/or P-glycoprotein substrate drugs can be increased by concomitant administration of CYP3A inhibitors and/or P-glycoprotein inhibitors. We believe that further understanding the physiology and biochemistry of the interactive nature of intestinal CYP3A and P-glycoprotein will be important in defining, controlling, and improving oral bioavailability of CYP3A/P-glycoprotein substrates.
Literature
1.
go back to reference Benet LZ, Wu CY, Hebert MF, et al. Intestinal drag metabolism and antitransport processes: a potential paradigm shift in oral drug delivery. J Controlled Release 1996; 39: 139–43CrossRef Benet LZ, Wu CY, Hebert MF, et al. Intestinal drag metabolism and antitransport processes: a potential paradigm shift in oral drug delivery. J Controlled Release 1996; 39: 139–43CrossRef
2.
go back to reference Wacher VJ, Wu CY, Benet LZ. Overlapping substrate specificities and tissue distribution of cytochrome P450 3A and P-glycoprotein: implications for drug delivery and activity in cancer chemotherapy. Mol Carcinog 1995; 13: 129–34PubMedCrossRef Wacher VJ, Wu CY, Benet LZ. Overlapping substrate specificities and tissue distribution of cytochrome P450 3A and P-glycoprotein: implications for drug delivery and activity in cancer chemotherapy. Mol Carcinog 1995; 13: 129–34PubMedCrossRef
3.
go back to reference Schuetz EG, Beck WT, Schuetz JD. Modulators and substrates of P-glycoprotein and cytochrome P4503A coordinately up-regulate these proteins in human colon carcinoma cells. Mol Pharmacol 1996; 49:311–8PubMed Schuetz EG, Beck WT, Schuetz JD. Modulators and substrates of P-glycoprotein and cytochrome P4503A coordinately up-regulate these proteins in human colon carcinoma cells. Mol Pharmacol 1996; 49:311–8PubMed
4.
go back to reference Kolars JC, Awni WM, Merion RM, et al. First-pass metabolism of cyclosporine by the gut. Lancet 1991; 338: 1488–90PubMedCrossRef Kolars JC, Awni WM, Merion RM, et al. First-pass metabolism of cyclosporine by the gut. Lancet 1991; 338: 1488–90PubMedCrossRef
5.
go back to reference Paine MF, Shen DD, Kunze KL, et al. First-pass metabolism of midazolam by the human intestine. Clin Pharmacol Ther 1996; 60: 14–24PubMedCrossRef Paine MF, Shen DD, Kunze KL, et al. First-pass metabolism of midazolam by the human intestine. Clin Pharmacol Ther 1996; 60: 14–24PubMedCrossRef
6.
go back to reference Thummel KE, O’shea D, Paine MF, et al. Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism. Clin Pharmacol Ther 1996;59:491–502PubMedCrossRef Thummel KE, O’shea D, Paine MF, et al. Oral first-pass elimination of midazolam involves both gastrointestinal and hepatic CYP3A-mediated metabolism. Clin Pharmacol Ther 1996;59:491–502PubMedCrossRef
7.
go back to reference Lown KS, Mayo RR, Leichtman AB, et al. Role of intestinal P-glycoprotein (mdr 1 ) in interpatient variation in the oral bioavailability of cyclosporine A. Clin Pharmacol Ther 1997; 62: 248–60PubMedCrossRef Lown KS, Mayo RR, Leichtman AB, et al. Role of intestinal P-glycoprotein (mdr 1 ) in interpatient variation in the oral bioavailability of cyclosporine A. Clin Pharmacol Ther 1997; 62: 248–60PubMedCrossRef
8.
go back to reference Masuda S, Uemoto S, Hashida T, et al. Effect of intestinal P-glycoprotein on daily tacrolimus trough level in a living-donor small bowel recipient. Clin Pharmacol Ther 2000; 68: 98–103PubMedCrossRef Masuda S, Uemoto S, Hashida T, et al. Effect of intestinal P-glycoprotein on daily tacrolimus trough level in a living-donor small bowel recipient. Clin Pharmacol Ther 2000; 68: 98–103PubMedCrossRef
9.
go back to reference Gomez DY, Wacher VJ, Tomlanovich SJ, et al. The effects of ketoconazole on the intestinal metabolism and bioavailability of cyclosporine. Clin Pharmacol Ther 1995; 58: 15–9PubMedCrossRef Gomez DY, Wacher VJ, Tomlanovich SJ, et al. The effects of ketoconazole on the intestinal metabolism and bioavailability of cyclosporine. Clin Pharmacol Ther 1995; 58: 15–9PubMedCrossRef
10.
go back to reference Floren LC, Bekersky I, Benet LZ, et al. Tacrolimus oral bioavailability doubles with coadministration of ketoconazole. Clin Pharmacol Ther 1997; 62: 41–9PubMedCrossRef Floren LC, Bekersky I, Benet LZ, et al. Tacrolimus oral bioavailability doubles with coadministration of ketoconazole. Clin Pharmacol Ther 1997; 62: 41–9PubMedCrossRef
11.
go back to reference Floren LC, Christians U, Zimmerman JJ, et al. Sirolimus oral bioavailability increases ten-fold with concomitant ketoconazole. Clin Pharmacol Ther 1999; 65: 159CrossRef Floren LC, Christians U, Zimmerman JJ, et al. Sirolimus oral bioavailability increases ten-fold with concomitant ketoconazole. Clin Pharmacol Ther 1999; 65: 159CrossRef
12.
go back to reference Westphal K, Weinbrenner A, Giessmann T, et al. Oral bioavailability of digoxin is enhanced by talinolol: evidence for involvement of intestinal P-glycoprotein. Clin Pharmacol Ther 2000; 68: 6–12PubMedCrossRef Westphal K, Weinbrenner A, Giessmann T, et al. Oral bioavailability of digoxin is enhanced by talinolol: evidence for involvement of intestinal P-glycoprotein. Clin Pharmacol Ther 2000; 68: 6–12PubMedCrossRef
13.
go back to reference Boyd RA, Stern RH, Stewart BH, et al. Atorvastatin coadministration may increase digoxin concentrations by inhibition of intestinal P-glycoprotein-mediated secretion. J Clin Pharmacol 2000; 40: 91–8PubMedCrossRef Boyd RA, Stern RH, Stewart BH, et al. Atorvastatin coadministration may increase digoxin concentrations by inhibition of intestinal P-glycoprotein-mediated secretion. J Clin Pharmacol 2000; 40: 91–8PubMedCrossRef
14.
go back to reference Hebert MF, Roberts JP, Prueksaritanont T, et al. Bioavailability of cyclosporine with concomitant rifampin administration is markedly less than predicted by hepatic enzyme induction. Clin Pharmacol Ther 1992; 52: 453–7PubMedCrossRef Hebert MF, Roberts JP, Prueksaritanont T, et al. Bioavailability of cyclosporine with concomitant rifampin administration is markedly less than predicted by hepatic enzyme induction. Clin Pharmacol Ther 1992; 52: 453–7PubMedCrossRef
15.
go back to reference Hebert MF, Fisher RM, Marsh CL, et al. Effects of rifampin on tacrolimus pharmacokinetics in healthy volunteers. J Clin Pharmacol 1999;39:91–6PubMedCrossRef Hebert MF, Fisher RM, Marsh CL, et al. Effects of rifampin on tacrolimus pharmacokinetics in healthy volunteers. J Clin Pharmacol 1999;39:91–6PubMedCrossRef
16.
go back to reference Backman JT, Olkkola KT, Neuvonen PJ. Rifampin drastically reduces plasma concentrations and effects of oral midazolam. Clin Pharmacol Ther 1996; 59: 7–13PubMedCrossRef Backman JT, Olkkola KT, Neuvonen PJ. Rifampin drastically reduces plasma concentrations and effects of oral midazolam. Clin Pharmacol Ther 1996; 59: 7–13PubMedCrossRef
17.
go back to reference Holtbecker N, Fromm MF, Kroemer HK, et al. The nifedipinerifampin interaction, evidence for induction of gut wall metabolism. Drag Metab Dispos 1996; 24: 1121–3 Holtbecker N, Fromm MF, Kroemer HK, et al. The nifedipinerifampin interaction, evidence for induction of gut wall metabolism. Drag Metab Dispos 1996; 24: 1121–3
18.
go back to reference van Asperen J, van Tellingen O, Sparreboom A, et al. Enhanced oral bioavailability of paclitaxel in mice treated with the P-glycoprotein blocker SDZ PSC 833. Br J Cancer 1997; 76: 1181–3PubMedCrossRef van Asperen J, van Tellingen O, Sparreboom A, et al. Enhanced oral bioavailability of paclitaxel in mice treated with the P-glycoprotein blocker SDZ PSC 833. Br J Cancer 1997; 76: 1181–3PubMedCrossRef
19.
go back to reference Yamaji H, Matsumura Y, Yoshikawa Y, et al. Pharmacokinetic interactions between HIV protease inhibitors in rats. Biopharm Drug Dispos 1999; 20: 241–7PubMedCrossRef Yamaji H, Matsumura Y, Yoshikawa Y, et al. Pharmacokinetic interactions between HIV protease inhibitors in rats. Biopharm Drug Dispos 1999; 20: 241–7PubMedCrossRef
20.
go back to reference Lin JH, Chiba M, Chen I, et al. Effect of dexamethasone on the intestinal first-pass metabolism of indinavir in rats: evidence of cytochrome P-450 3A and P-glycoprotein induction. Drug Metab Dispos 1999; 27: 1187–93PubMed Lin JH, Chiba M, Chen I, et al. Effect of dexamethasone on the intestinal first-pass metabolism of indinavir in rats: evidence of cytochrome P-450 3A and P-glycoprotein induction. Drug Metab Dispos 1999; 27: 1187–93PubMed
21.
go back to reference Salphati L, Benet LZ. Effects of ketoconazole on digoxin absorption and disposition in rats. Pharmacology 1998;56: 308–13PubMedCrossRef Salphati L, Benet LZ. Effects of ketoconazole on digoxin absorption and disposition in rats. Pharmacology 1998;56: 308–13PubMedCrossRef
22.
go back to reference Song S, Suzuki H, Kawai R, et al. Effect of PSC 833, a P-glycoprotein modulator, on the disposition of vincristine and digoxin in rats. Drag Metab Dispos 1999; 27: 689–94 Song S, Suzuki H, Kawai R, et al. Effect of PSC 833, a P-glycoprotein modulator, on the disposition of vincristine and digoxin in rats. Drag Metab Dispos 1999; 27: 689–94
23.
go back to reference Zhang Y, Hsien Y, Izumi T, et al. Effects of ketoconazole on the intestinal metabolism, transport and oral bioavailability of K02, a novel vinylsulfone peptidomimetic cysteine protease inhibitor and a P450 3A, P-glycoprotein dual substrate, in male Sprague-Dawley rats. J Pharmacol Exp Ther 1998; 287: 246–52PubMed Zhang Y, Hsien Y, Izumi T, et al. Effects of ketoconazole on the intestinal metabolism, transport and oral bioavailability of K02, a novel vinylsulfone peptidomimetic cysteine protease inhibitor and a P450 3A, P-glycoprotein dual substrate, in male Sprague-Dawley rats. J Pharmacol Exp Ther 1998; 287: 246–52PubMed
24.
go back to reference Wrighton SA, VandenBranden M, Ring BJ. The human drag metabolizing cytochromes P450. J Pharmacokinet Biopharm 1996; 24: 461–73PubMed Wrighton SA, VandenBranden M, Ring BJ. The human drag metabolizing cytochromes P450. J Pharmacokinet Biopharm 1996; 24: 461–73PubMed
25.
go back to reference Benet LZ, Kroetz DL, Sheiner LB. Pharmacokinetics: the dynamics of drug absorption, distribution, and elimination. In: Hardman JH, Limbird LE, Molinoff PB, et al., editors. Goodman & Gilman’s the pharmacological basis of therapeutics. New York: McGraw-Hill, 1996: 3–28 Benet LZ, Kroetz DL, Sheiner LB. Pharmacokinetics: the dynamics of drug absorption, distribution, and elimination. In: Hardman JH, Limbird LE, Molinoff PB, et al., editors. Goodman & Gilman’s the pharmacological basis of therapeutics. New York: McGraw-Hill, 1996: 3–28
26.
go back to reference Murray GI, Barnes TS, Sewell HF, et al. The immunocytochemical localization and distribution of cytochrome P-450 in normal human hepatic and extrahepatic tissues with a monoclonal antibody to human cytochrome P-450. Br J Clin Pharmacol 1988; 25: 465–75PubMedCrossRef Murray GI, Barnes TS, Sewell HF, et al. The immunocytochemical localization and distribution of cytochrome P-450 in normal human hepatic and extrahepatic tissues with a monoclonal antibody to human cytochrome P-450. Br J Clin Pharmacol 1988; 25: 465–75PubMedCrossRef
27.
go back to reference Haehner BD, Gorski JC, Vandenbranden M, et al. Bimodal distribution of renal cytochrome P450 3A activity in humans. Mol Pharmacol 1996; 50: 52–9PubMed Haehner BD, Gorski JC, Vandenbranden M, et al. Bimodal distribution of renal cytochrome P450 3A activity in humans. Mol Pharmacol 1996; 50: 52–9PubMed
28.
go back to reference Kolars JC, Schmiedlin-Ren P, Schuetz JD, et al. Identification of rifampin-inducible P450IIIA4 (CYP3A4) in human small bowel enterocytes. J Clin Invest 1992; 90: 1871–8PubMedCrossRef Kolars JC, Schmiedlin-Ren P, Schuetz JD, et al. Identification of rifampin-inducible P450IIIA4 (CYP3A4) in human small bowel enterocytes. J Clin Invest 1992; 90: 1871–8PubMedCrossRef
29.
go back to reference Shimada T, Yamazaki H, Mimura M, et al. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Caucasians. J Pharmacol Exp Ther 1994; 270: 414–23PubMed Shimada T, Yamazaki H, Mimura M, et al. Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Caucasians. J Pharmacol Exp Ther 1994; 270: 414–23PubMed
30.
go back to reference Watkins PB, Wrighton SA, Schuetz EG, et al. Identification of glucocorticoid-inducible cytochrome P-450 in the intestine mucosa of rats and human. J Clin Invest 1987; 80: 1029–36PubMedCrossRef Watkins PB, Wrighton SA, Schuetz EG, et al. Identification of glucocorticoid-inducible cytochrome P-450 in the intestine mucosa of rats and human. J Clin Invest 1987; 80: 1029–36PubMedCrossRef
31.
go back to reference Williams JA, Chenery RJ, Berkhout TA, et al. Induction of cytochrome P4503A by the antiglucocorticoid mifepristone and a novel hypocholesterolaemic drug. Drug Metab Dispos 1997; 25: 757–61PubMed Williams JA, Chenery RJ, Berkhout TA, et al. Induction of cytochrome P4503A by the antiglucocorticoid mifepristone and a novel hypocholesterolaemic drug. Drug Metab Dispos 1997; 25: 757–61PubMed
32.
go back to reference Lown KS, Kolars JC, Thummel KE, et al. Interpatient heterogeneity in expression of CYP3A4 and CYP3A5 in small bowel. Lack of prediction by the erythromycin breath test. Drug Metab Dispos 1994; 22: 947–55PubMed Lown KS, Kolars JC, Thummel KE, et al. Interpatient heterogeneity in expression of CYP3A4 and CYP3A5 in small bowel. Lack of prediction by the erythromycin breath test. Drug Metab Dispos 1994; 22: 947–55PubMed
33.
go back to reference Lehmann JM, McKee DD, Waston MA, et al. The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions. J Clin Invest 1998; 102: 1016–23PubMedCrossRef Lehmann JM, McKee DD, Waston MA, et al. The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions. J Clin Invest 1998; 102: 1016–23PubMedCrossRef
34.
go back to reference Blumberg B, Sabbagh Jr W, Juguilon H, et al. SXR, a novel steroid and xenobiotic-sensing nuclear receptor. Genes Dev 1998; 12: 3195–205PubMedCrossRef Blumberg B, Sabbagh Jr W, Juguilon H, et al. SXR, a novel steroid and xenobiotic-sensing nuclear receptor. Genes Dev 1998; 12: 3195–205PubMedCrossRef
35.
go back to reference Bertilsson G, Heidrich J, Svensson K, et al. Identification of a human nuclear receptor defines a new signaling pathway for CYP3 A induction. Proc Natl Acad Sci USA 1998; 95: 12208–13PubMedCrossRef Bertilsson G, Heidrich J, Svensson K, et al. Identification of a human nuclear receptor defines a new signaling pathway for CYP3 A induction. Proc Natl Acad Sci USA 1998; 95: 12208–13PubMedCrossRef
36.
go back to reference Chiba M, Hensleigh M, Lin JH. Hepatic and intestinal metabolism of indinavir, an HIV protease inhibitor, in rat and human microsomes. Major role of CYP3A. Biochem Pharmacol 1997; 53: 1187–95PubMedCrossRef Chiba M, Hensleigh M, Lin JH. Hepatic and intestinal metabolism of indinavir, an HIV protease inhibitor, in rat and human microsomes. Major role of CYP3A. Biochem Pharmacol 1997; 53: 1187–95PubMedCrossRef
37.
go back to reference Fitzsimmons ME, Collins JM. Selective biotransformation of the human immunodeficiency virus protease inhibitor saquinavir by human small-intestinal cytochrome P4503A4: potential contribution to high first-pass metabolism. Drug Metab Dispos 1997; 25: 256–66PubMed Fitzsimmons ME, Collins JM. Selective biotransformation of the human immunodeficiency virus protease inhibitor saquinavir by human small-intestinal cytochrome P4503A4: potential contribution to high first-pass metabolism. Drug Metab Dispos 1997; 25: 256–66PubMed
38.
go back to reference Kumar GN, Rodrigues AD, Buko AM, et al. Cytochrome P450-mediated metabolism of the HJV-1 protease inhibitor ritonavir (ABT-538) in human liver microsomes. J Pharmacol Exp Ther 1996; 277: 423–31PubMed Kumar GN, Rodrigues AD, Buko AM, et al. Cytochrome P450-mediated metabolism of the HJV-1 protease inhibitor ritonavir (ABT-538) in human liver microsomes. J Pharmacol Exp Ther 1996; 277: 423–31PubMed
39.
go back to reference Li AP, Kaminski DL, Rasmussen A. Substrates of human hepatic cytochrome P450 3A4. Toxicology 1995; 104: 1–8PubMedCrossRef Li AP, Kaminski DL, Rasmussen A. Substrates of human hepatic cytochrome P450 3A4. Toxicology 1995; 104: 1–8PubMedCrossRef
41.
go back to reference Smith DA, Jones BC. Speculations on the substrate structureactivity relationship (SSAR) of cytochrome P450 enzymes. Biochem Pharmacol 1992; 44: 2089–98PubMedCrossRef Smith DA, Jones BC. Speculations on the substrate structureactivity relationship (SSAR) of cytochrome P450 enzymes. Biochem Pharmacol 1992; 44: 2089–98PubMedCrossRef
42.
go back to reference Ferenczy GG, Morris GM. The active site of cytochrome P-450 nifedipine oxidase: a model-building study. J Mol Graph 1989;7:206–11PubMedCrossRef Ferenczy GG, Morris GM. The active site of cytochrome P-450 nifedipine oxidase: a model-building study. J Mol Graph 1989;7:206–11PubMedCrossRef
43.
go back to reference Shou M, Grogan J, Mancewicz JA, et al. Activation of CYP3A4: evidence for the simultaneous binding of two substrates in a cytochrome P450 active site. Biochemistry 1994; 33: 6450–5PubMedCrossRef Shou M, Grogan J, Mancewicz JA, et al. Activation of CYP3A4: evidence for the simultaneous binding of two substrates in a cytochrome P450 active site. Biochemistry 1994; 33: 6450–5PubMedCrossRef
44.
go back to reference de Waziers PH, Cugnenc PH, Yang CS, et al. Cytochrome P450 isoenzymes, epoxide hydrolase and glutathione transferases in rat and human hepatic and extrahepatic tissues. J Pharmacol Exp Ther 1990; 253: 387–94PubMed de Waziers PH, Cugnenc PH, Yang CS, et al. Cytochrome P450 isoenzymes, epoxide hydrolase and glutathione transferases in rat and human hepatic and extrahepatic tissues. J Pharmacol Exp Ther 1990; 253: 387–94PubMed
45.
go back to reference Paine MF, Khalighi M, Fisher JM, et al. Characterization of interintestinal and intraintestinal variations in human CYP3A-dependent metabolism. J Pharmacol Exp Ther 1997; 283: 1552–62PubMed Paine MF, Khalighi M, Fisher JM, et al. Characterization of interintestinal and intraintestinal variations in human CYP3A-dependent metabolism. J Pharmacol Exp Ther 1997; 283: 1552–62PubMed
46.
go back to reference Wacher VJ, Silverman JA, Zhang Y, et al. Role of P-glycoprotein and cytochrome P450 3A in limiting oral absorption of Peptides and peptidomimetics. J Pharm Sci 1998;87: 1322–30PubMedCrossRef Wacher VJ, Silverman JA, Zhang Y, et al. Role of P-glycoprotein and cytochrome P450 3A in limiting oral absorption of Peptides and peptidomimetics. J Pharm Sci 1998;87: 1322–30PubMedCrossRef
47.
go back to reference Lown KS, Ghosh M, Watkins PB. Sequence of intestinal and hepatic cytochrome P450 3A4 cDNAs are identical. Drug Metab Dispos 1998; 26: 185–7PubMed Lown KS, Ghosh M, Watkins PB. Sequence of intestinal and hepatic cytochrome P450 3A4 cDNAs are identical. Drug Metab Dispos 1998; 26: 185–7PubMed
48.
49.
go back to reference Juliano RL, Ling V. A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants. Biochim Biophys Acta 1976; 455: 152–62PubMedCrossRef Juliano RL, Ling V. A surface glycoprotein modulating drug permeability in Chinese hamster ovary cell mutants. Biochim Biophys Acta 1976; 455: 152–62PubMedCrossRef
50.
go back to reference Patel NH, Rothenberg ML. Multidrug resistance in cancer chemotherapy. Invest New Drugs 1994; 12: 1–13PubMedCrossRef Patel NH, Rothenberg ML. Multidrug resistance in cancer chemotherapy. Invest New Drugs 1994; 12: 1–13PubMedCrossRef
51.
go back to reference Gottesman MM, Pastan I. Biochemistry of multidrug resistance mediated by the multidrug transporter. Annu Rev Biochem 1993; 62: 385–427PubMedCrossRef Gottesman MM, Pastan I. Biochemistry of multidrug resistance mediated by the multidrug transporter. Annu Rev Biochem 1993; 62: 385–427PubMedCrossRef
52.
go back to reference Silverman JA, Schrenk D. Hepatic canalicular membrane 4: expression of the multidrug resistance genes in the liver. FASEB J 1997; 11:308–13PubMed Silverman JA, Schrenk D. Hepatic canalicular membrane 4: expression of the multidrug resistance genes in the liver. FASEB J 1997; 11:308–13PubMed
53.
go back to reference Cordon-Cardo C, O’Brien JP, Boccia J, et al. Expression of the multidrug resistance gene product (P-glycoprotein) in human normal and tumor tissues. J Histochem Cytochem 1990; 38: 1277–87PubMedCrossRef Cordon-Cardo C, O’Brien JP, Boccia J, et al. Expression of the multidrug resistance gene product (P-glycoprotein) in human normal and tumor tissues. J Histochem Cytochem 1990; 38: 1277–87PubMedCrossRef
54.
go back to reference Thiebaut F, Tsuruo T, Hamada H, et al. Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues. Proc Natl Acad Sci USA 1987; 84:7735–8PubMedCrossRef Thiebaut F, Tsuruo T, Hamada H, et al. Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues. Proc Natl Acad Sci USA 1987; 84:7735–8PubMedCrossRef
55.
go back to reference Schinkel AH, Smit JJ, van Teilingen O, et al. Disruption of the mouse mdrla P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs. Cell 1994; 77: 491–502PubMedCrossRef Schinkel AH, Smit JJ, van Teilingen O, et al. Disruption of the mouse mdrla P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs. Cell 1994; 77: 491–502PubMedCrossRef
56.
go back to reference Schinkel AH, Mol CA, Wagenaar E, et al. Multidrug resistance and the role of P-glycoprotein knockout mice. Eur J Cancer 1995; 31A: 1295–8PubMedCrossRef Schinkel AH, Mol CA, Wagenaar E, et al. Multidrug resistance and the role of P-glycoprotein knockout mice. Eur J Cancer 1995; 31A: 1295–8PubMedCrossRef
57.
go back to reference Schumacher U, Mollgard K. The multidrug-resistance P-glycoprotein (Pgp, MDR1) is an early marker of blood-brain barrier development in the microvessels of the developing human brain. Histochem Cell Biol 1997; 108: 179–82PubMedCrossRef Schumacher U, Mollgard K. The multidrug-resistance P-glycoprotein (Pgp, MDR1) is an early marker of blood-brain barrier development in the microvessels of the developing human brain. Histochem Cell Biol 1997; 108: 179–82PubMedCrossRef
58.
go back to reference Schuetz EG, Schinkel AH, Relling MV, et al. P-glycoprotein, a major determinant of rifampicin-inducible expression of cytochrome P450 3A in mice and humans. Proc Natl Acad Sci USA 1996; 93: 4001–5PubMedCrossRef Schuetz EG, Schinkel AH, Relling MV, et al. P-glycoprotein, a major determinant of rifampicin-inducible expression of cytochrome P450 3A in mice and humans. Proc Natl Acad Sci USA 1996; 93: 4001–5PubMedCrossRef
59.
go back to reference Silverman JA, Thorgeirsson SS. Regulation and function of the multidrug resistance genes in liver. Prog Liver Dis 1995; 13: 101–23PubMed Silverman JA, Thorgeirsson SS. Regulation and function of the multidrug resistance genes in liver. Prog Liver Dis 1995; 13: 101–23PubMed
60.
go back to reference Rosenberg MF, Callaghan R, Ford RC, et al. Structure of the multidrug resistance P-glycoprotein to 2.5 nm resolution determined by electron microscopy and image analysis. J Biol Chem 1997; 272: 10685–94PubMedCrossRef Rosenberg MF, Callaghan R, Ford RC, et al. Structure of the multidrug resistance P-glycoprotein to 2.5 nm resolution determined by electron microscopy and image analysis. J Biol Chem 1997; 272: 10685–94PubMedCrossRef
61.
go back to reference Fojo AT, Ueda K, Slamon DJ, et al. Expression of a multidrugresistance gene in human tumors and tissues. Proc Natl Acad Sci USA 1987; 84: 265–9PubMedCrossRef Fojo AT, Ueda K, Slamon DJ, et al. Expression of a multidrugresistance gene in human tumors and tissues. Proc Natl Acad Sci USA 1987; 84: 265–9PubMedCrossRef
62.
go back to reference Sparreboom A, van Asperen J, Mayer U, et al. Limited oral bioavailability and active epithelial excretion of paclitaxel (Taxol) caused by P-glycoprotein in the intestine. Proc Natl Acad Sci USA 1997; 94: 2031–5PubMedCrossRef Sparreboom A, van Asperen J, Mayer U, et al. Limited oral bioavailability and active epithelial excretion of paclitaxel (Taxol) caused by P-glycoprotein in the intestine. Proc Natl Acad Sci USA 1997; 94: 2031–5PubMedCrossRef
63.
go back to reference Kim RB, Fromm MF, Wandel C, et al. The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors. J Clin Invest 1998; 101: 289–94PubMedCrossRef Kim RB, Fromm MF, Wandel C, et al. The drug transporter P-glycoprotein limits oral absorption and brain entry of HIV-1 protease inhibitors. J Clin Invest 1998; 101: 289–94PubMedCrossRef
64.
go back to reference Kim RB, Wandel C, Leake B, et al. Interrelationship between substrates and inhibitors of human CYP3A and P-glycoprotein. Pharm Res 1999; 16: 408–14PubMedCrossRef Kim RB, Wandel C, Leake B, et al. Interrelationship between substrates and inhibitors of human CYP3A and P-glycoprotein. Pharm Res 1999; 16: 408–14PubMedCrossRef
65.
go back to reference Benet LZ, Izumi T, Zhang Y, et al. Intestinal MDR transport proteins and P-450 enzymes as barriers to oral drug delivery. J Controlled Release 1999; 62: 25–31CrossRef Benet LZ, Izumi T, Zhang Y, et al. Intestinal MDR transport proteins and P-450 enzymes as barriers to oral drug delivery. J Controlled Release 1999; 62: 25–31CrossRef
66.
go back to reference Palkama VJ, Ahonen J, Neuvonen PJ, et al. Effect of saquinavir on the pharmacokinetics and pharmacodynamics of oral and intravenous midazolam. Clin Pharmacol Ther 1999; 66: 33–9PubMedCrossRef Palkama VJ, Ahonen J, Neuvonen PJ, et al. Effect of saquinavir on the pharmacokinetics and pharmacodynamics of oral and intravenous midazolam. Clin Pharmacol Ther 1999; 66: 33–9PubMedCrossRef
67.
go back to reference Heizmann P, Ziegler WH. Excretion and metabolism of 14C-midazolam in humans following oral dosing. Arzneimittel Forschung 1981; 31: 2220–3PubMed Heizmann P, Ziegler WH. Excretion and metabolism of 14C-midazolam in humans following oral dosing. Arzneimittel Forschung 1981; 31: 2220–3PubMed
68.
go back to reference Wu CY, Benet LZ, Hebert MF, et al. Differentiation of absorption and first-pass gut and hepatic metabolism in humans: studies with cyclosporine. Clin Pharmacol Ther 1995; 58: 492–7PubMedCrossRef Wu CY, Benet LZ, Hebert MF, et al. Differentiation of absorption and first-pass gut and hepatic metabolism in humans: studies with cyclosporine. Clin Pharmacol Ther 1995; 58: 492–7PubMedCrossRef
69.
go back to reference Kronbach T, Mathys D, Umeno M, et al. Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4. Mol Pharmacol 1989; 36: 89–96PubMed Kronbach T, Mathys D, Umeno M, et al. Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4. Mol Pharmacol 1989; 36: 89–96PubMed
70.
go back to reference Gorski JC, Jones DR, Haehner-Daniels BD, et al. The contribution of intestinal and hepatic CYP3A to the interaction between midazolam and Clarithromycin. Clin Pharmacol Ther 1998; 64: 133–43PubMedCrossRef Gorski JC, Jones DR, Haehner-Daniels BD, et al. The contribution of intestinal and hepatic CYP3A to the interaction between midazolam and Clarithromycin. Clin Pharmacol Ther 1998; 64: 133–43PubMedCrossRef
71.
go back to reference Greiner B, Eichelbaum M, Fritz P, et al. The role of intestinal P-glycoprotein in the interaction of digoxin and rifampin. J Clin Invest 1999; 104: 147–53PubMedCrossRef Greiner B, Eichelbaum M, Fritz P, et al. The role of intestinal P-glycoprotein in the interaction of digoxin and rifampin. J Clin Invest 1999; 104: 147–53PubMedCrossRef
72.
go back to reference Hoffmeyer S, Burk O, von Richter O, et al. Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proc Natl Acad Sci USA 2000; 97: 3473–8PubMedCrossRef Hoffmeyer S, Burk O, von Richter O, et al. Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proc Natl Acad Sci USA 2000; 97: 3473–8PubMedCrossRef
73.
go back to reference Takanaga H, Ohnishi A, Yamada S, et al. Polymethoxylated flavones in orange juice are inhibitors of P-glycoprotein but not cytochrome P450 3A4. J Pharmacol Exp Ther 2000; 293: 230–6PubMed Takanaga H, Ohnishi A, Yamada S, et al. Polymethoxylated flavones in orange juice are inhibitors of P-glycoprotein but not cytochrome P450 3A4. J Pharmacol Exp Ther 2000; 293: 230–6PubMed
74.
go back to reference Dantzig AH, Shepard RL, Law KL, et al. Selectivity of the multidrug resistance modulator, LY335979, for P-glycoprotein and effect on cytochrome P-450 activities. J Pharmacol Exp Ther 1999; 290: 854–62PubMed Dantzig AH, Shepard RL, Law KL, et al. Selectivity of the multidrug resistance modulator, LY335979, for P-glycoprotein and effect on cytochrome P-450 activities. J Pharmacol Exp Ther 1999; 290: 854–62PubMed
75.
go back to reference Achira M, Suzuki H, Ito K, et al. Comparative studies to determine selective inhibitor for P-glycoprotein and cytochrome P450 3A4 [online]. AAPS PharmSci 2000; 4 Achira M, Suzuki H, Ito K, et al. Comparative studies to determine selective inhibitor for P-glycoprotein and cytochrome P450 3A4 [online]. AAPS PharmSci 2000; 4
76.
go back to reference Hall SD, Thummel KE, Watkins PB, et al. Molecular and physical mechanisms of first-pass extraction. J Pharmacol Exp Ther 1999; 27: 161–6 Hall SD, Thummel KE, Watkins PB, et al. Molecular and physical mechanisms of first-pass extraction. J Pharmacol Exp Ther 1999; 27: 161–6
77.
go back to reference Bailey DG, Malcolm J, Arnold O, et al. Grapefruit juice-drug interactions. Br J Clin Pharmacol 1998; 46: 101–10PubMedCrossRef Bailey DG, Malcolm J, Arnold O, et al. Grapefruit juice-drug interactions. Br J Clin Pharmacol 1998; 46: 101–10PubMedCrossRef
78.
go back to reference Lown KS, Bailey DG, Fontana RJ, et al. Grapefruit juice increases felodipine oral availability in humans by decreasing intestinal CYP3A protein expression. J Clin Invest 1997; 99: 2545–53PubMedCrossRef Lown KS, Bailey DG, Fontana RJ, et al. Grapefruit juice increases felodipine oral availability in humans by decreasing intestinal CYP3A protein expression. J Clin Invest 1997; 99: 2545–53PubMedCrossRef
79.
go back to reference Ito K, Kusuhara H, Sugiyama Y Effects of intestinal CYP3A4 and P-glycoprotein on oral drug absorption: theoretical approach. Pharm Res 1999; 16: 225–31PubMedCrossRef Ito K, Kusuhara H, Sugiyama Y Effects of intestinal CYP3A4 and P-glycoprotein on oral drug absorption: theoretical approach. Pharm Res 1999; 16: 225–31PubMedCrossRef
80.
go back to reference Almquist KC, Loe DW, Hipfner DR, et al. Characterization of the M(r) 190,000 multidrug resistance protein (MRP) in drugselected and transfected human tumor cell. Cancer Res 1995; 55: 102–10PubMed Almquist KC, Loe DW, Hipfner DR, et al. Characterization of the M(r) 190,000 multidrug resistance protein (MRP) in drugselected and transfected human tumor cell. Cancer Res 1995; 55: 102–10PubMed
81.
go back to reference Adibi SA. The Oligopeptide transporter (Pept-1) in human intestine: biology and function. Gastroenterology 1997; 113: 332–40PubMedCrossRef Adibi SA. The Oligopeptide transporter (Pept-1) in human intestine: biology and function. Gastroenterology 1997; 113: 332–40PubMedCrossRef
82.
go back to reference Zhang L, Dresser MJ, Gray AT, et al. Cloning and functional expression of a human liver organic cation transporter. Mol Pharmacol 1997;51:913–21PubMed Zhang L, Dresser MJ, Gray AT, et al. Cloning and functional expression of a human liver organic cation transporter. Mol Pharmacol 1997;51:913–21PubMed
Metadata
Title
The Gut as a Barrier to Drug Absorption
Combined Role of Cytochrome P450 3A and P-Glycoprotein
Authors
Dr Yuanchao Zhang
Leslie Z. Benet
Publication date
01-03-2001
Publisher
Springer International Publishing
Published in
Clinical Pharmacokinetics / Issue 3/2001
Print ISSN: 0312-5963
Electronic ISSN: 1179-1926
DOI
https://doi.org/10.2165/00003088-200140030-00002

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