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Serum Rifampicin Levels in Patients with Tuberculosis

Effect of P-Glycoprotein and CYP3A4 Blockers on its Absorption

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Abstract

Objective: To identify patients with tuberculosis (TB) showing poor bioavailability for rifampicin and to delineate the role of possible factors such as overexpression of intestinal cytochrome P450 3A4 (CYP3A4) and P-glycoprotein (PGP) in the drug’s bioavailability by administering known blockers.

Patients, design and setting: 77 clinically proven TB patients were included in this nonblinded, randomised, comparative trial carried out at one centre at the All India Institute of Medical Sciences, New Delhi, India.

Interventions: The concentrations of rifampicin and its active metabolite, 25-desacetylrifampicin (DRMP), were measured in blood samples of the 77 TB patients at 0, 1, 2 and 4 hours after their usual morning rifampicin dose. Of these, 19 patients showing the lowest area under the concentration-time curve values from 0 to 4 hours after administration (AUC0–4) were selected and pretreated with a single dose of either verapamil (80mg) or itraconazole (200mg) as both PGP and CYP3A4 blockers 1 hour prior to rifampicin administration. Rifampicin and DRMP concentrations were estimated using high performance liquid chromatography in all serum samples collected at the same timepoints.

Main outcome measures and results: A statistically significant increase (p <0.05) was found both in the serum levels of rifampicin at 2 hours and in the AUC0–4 values (158% and 84%, respectively) after pretreatment with verapamil. However, an increase in the levels of rifampicin was found to be insignificant on pretreatment with itraconazole. The estimated levels of DRMP also supported these results.

Conclusions: The increase in rifampicin levels on administration of a PGP/ CYP3A4 blocker suggests a pivotal role for PGP/CYP3A4 in the absorption of rifampicin in patients with TB, which may be responsible for lower or variable levels of rifampicin.

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  1. 1The use of tradenames is for product identification only and does not imply endorsement.

References

  1. Bastian I, Colebunders R. Treatment and prevention of multidrug-resistant tuberculosis. Drugs 1999; 58: 633–61

    Article  PubMed  CAS  Google Scholar 

  2. Chambers HF. Antimycobacterial drugs. In: Katzung BG, editor. Basic and clinical Pharmacology. Appleton & Lange, McGraw-Hill, SanFrancisco, USA, 2001: 803-13

  3. Hobby GL, Lenert TF. Observations on the action of rifampicin and ethambutol alone and in combination with other antituberculous drugs. Am Rev Respir Dis 1972; 105: 292–5

    PubMed  CAS  Google Scholar 

  4. Kimerling ME, Phillips P, Patterson P, et al. Low serum antimycobacterial drug levels in non-HIV-infected tuberculosis patients. Chest 1998; 113: 1178–83

    Article  PubMed  CAS  Google Scholar 

  5. Khilnani GC, Sharma SK, Pande JN. Multi drug resistant tuberculosis. Indian J Chest Dis Allied Sci 1994; 36: 137–45

    PubMed  CAS  Google Scholar 

  6. Polasa K, Krishnaswamy K. Effect of food on bioavailability of rifampicin. J Clin Pharmacol 1983; 23: 433–7

    PubMed  CAS  Google Scholar 

  7. Fromm MF, Busse D, Kroemer HK, et al. Differential induction of prehepatic and hepatic metabolism of verapamil by rifampicin. Hepatology 1996; 24: 796–801

    Article  PubMed  CAS  Google Scholar 

  8. Singh S, Mariappan TT, Shankar R, et al. Critical review of the probable reasons for the poor variable bioavailability of rifampicin from anti-tubercular fixed-dose combination (FDC) products, and the likely solutions to the problem. Int J Pharm 2001;228: 5–17

    Article  PubMed  CAS  Google Scholar 

  9. Kongara S, Velpandian T, Sinha S, et al. The effect of nutritional status on the single dose pharmacokinetics of RMP in tuberculosis patients [abstract]. Chest 2001; 120: 323S

    Google Scholar 

  10. Schuetz EG, Schinkel AH, Relling MV, et al. P-glycoprotein: a major determinant of rifampicin-inducible expression of cytochrome P4503A in mice and humans. Proc Natl Acad Sci USA 1996; 93: 4001–5

    Article  PubMed  CAS  Google Scholar 

  11. Greiner B, Eichelbaum M, Fritz P, et al. The role of intestinal Pglycoprotein in the interaction of digoxin and RMP. J Clin Invest 1999; 104: 147–53

    Article  PubMed  CAS  Google Scholar 

  12. Muller C, Bailly JD, Goubin F, et al. Verapamil decreases Pglycoprotein expression in multi-drug resistant human leukemic cell lines. Int J Cancer 1994; 56: 749–54

    Article  PubMed  CAS  Google Scholar 

  13. Tian R, Koyabu N, Takanaga H, et al. Effects of grapefruit juice and orange juice on the intestinal efflux of P-glycoprotein substrates. Pharm Res 2002; 19: 802–9

    Article  PubMed  CAS  Google Scholar 

  14. Yeo KR, Yeo WW. Inhibitory effects of verapamil and diltiazem on simvastatin metabolism in human liver microsomes. Br J Clin Pharmacol 2001; 51: 461–70

    Article  PubMed  CAS  Google Scholar 

  15. Ma B, Prueksaritanont T, Lin JH. Drug interactions with calcium channel blockers: possible involvement of metaboliteintermediate complexation with CYP3A. Drug Metab Dispos 2000; 28: 125–30

    PubMed  CAS  Google Scholar 

  16. Kaukonen KM, Olkkola KT, Neuvonen PJ. Itraconazole increases plasma concentrations of quinidine. Clin Pharmacol Ther 1997; 62: 510–7

    Article  PubMed  CAS  Google Scholar 

  17. Takara K, Tanigawara Y, Komada F, et al. Cellular pharmacokinetic aspects of reversal effect of itraconazole on P-glycoprotein-mediated resistance of anticancer drugs. Biol Pharm Bull1999; 22: 1355–9

    Article  PubMed  CAS  Google Scholar 

  18. Le Guellec C, Gaudet ML, Lamanetre S, et al. Stability of rifampicin in plasma: consequences for therapeutic monitoring and pharmacokinetic studies. Ther Drug Monit 1997; 19: 669–74

    Article  Google Scholar 

  19. Watkins PB. The barrier function of CYP3A4 and P-glycoprotein in the small bowel. Adv Drug Deliv Rev 1997; 27: 161–70

    Article  PubMed  CAS  Google Scholar 

  20. Gurumurthy P, Ramachandran G, Vijayalakshmi S, et al. Bioavailability of rifampicin, isoniazid and pyrazinamide in a triple drug formulation: comparison of plasma and urine kinetics. Int J Tuberc Lung Dis 1999; 3: 119–25

    PubMed  CAS  Google Scholar 

  21. Panchagnula R, Kaur KJ, Singh I, et al. Bioequivalence of rifampicin when administered as a fixed-dose combined formulation of four drugs versus separate formulations. Methods Find Exp Clin Pharmacol 2000; 22: 684–94

    Google Scholar 

  22. Padgaonkar KA, Revankar SN, Bhatt AD, et al. Comparative bioequivalence study of rifampicin and isoniazid combinations in healthy volunteers. Int J Tuberc Lung Dis 1999; 3: 627–31

    PubMed  CAS  Google Scholar 

  23. Shishoo CJ, Shah SA, Rathod IS, et al. Impaired bioavailability of rifampicin in the presence of isoniazid from a fixed dose combination (FDC) formulation. Int J Pharm 2001; 228(1–2): 53–67

    Article  PubMed  CAS  Google Scholar 

  24. Darbar D, Fromm MF, Dell’Orto S, et al. Modulation by dietary salt of verapamil disposition in humans. Circulation 1998; 98: 2702–8

    Article  PubMed  CAS  Google Scholar 

  25. Velpandian T, Jasuja R, Bhardwaj RK, et al. Piperine in food: interference in the pharmacokinetics of phenytoin. Eur J Drug Metab Pharmacokinet 2001; 26: 241–7

    Article  PubMed  CAS  Google Scholar 

  26. Bhardwaj RK, Glaeser H, Becquemont L, et al. Piperine, a major constituent of black pepper, inhibits human P-glycoprotein and CYP3A4. J Pharmacol Exp Ther 2002; 302: 645–50

    Article  PubMed  CAS  Google Scholar 

  27. 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 U S A 1987; 84: 7735–8

    Article  PubMed  CAS  Google Scholar 

  28. Shimada T, Yamazaki H, Mimura M, et al. Interindividual variations in human liver cytochrome P450 enzymes involved in oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Causasians. J Pharmacol Exp Ther 1994; 270: 414–23

    PubMed  CAS  Google Scholar 

  29. Pichard L, Fabre I, Fabre G, et al. Cyclosporin A drug interactions: screening for inducers and inhibitors of cytochrome P-450 (cyclosporin A oxidase) in primary cultures of human hepatocytes and in liver microsomes. Drug Metab Dispos 1990; 18: 595–606

    PubMed  CAS  Google Scholar 

  30. Lown KS, Mayo RR, Leichtman AB, et al. Role of intestinal Pglycoprotein (mdrl) in interpatient variation in the oral bioavailability of cyclosporine. Clin Pharmacol Ther 1997; 62: 248–60

    Article  PubMed  CAS  Google Scholar 

  31. 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: 1322–30

    Article  PubMed  CAS  Google Scholar 

  32. Hall JG, Cory AH, Cory JG. Lack of competition of substrates for P-glycoprotein in MCF-7 breast cancer cells overexpressing MDR1. Adv Enzyme Regul 1999; 39: 113–28

    Article  PubMed  CAS  Google Scholar 

  33. Zhang Y, Benet LZ. The gut as a barrier to drug absorption: combined role of cytochrome P450 3A and P-glycoprotein. Clin Pharmacokinet 2001; 40: 159–68

    Article  PubMed  CAS  Google Scholar 

  34. Cummins CL, Jacobsen W, Benet LZ. Unmasking the dynamic interplay between intestinal P-glycoprotein and CYP3A4. J Pharmacol Exp Ther 2002; 300: 1036–45

    Article  PubMed  CAS  Google Scholar 

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Acknowledgements

This study was funded by the Departments of Pharmacology and Medicine, All India Institute of Medical Sciences, New Delhi. The authors are very grateful to Dr Sanjeev Sinha and Dr Srikanth Kongara, Clinical Pharmacology, for their valuable help in recruiting patients with tuberculosis from the outpatient department.

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Correspondence to Jai Prakash.

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Prakash, J., Velpandian, T., Pande, J.N. et al. Serum Rifampicin Levels in Patients with Tuberculosis. Clin. Drug Investig. 23, 463–472 (2003). https://doi.org/10.2165/00044011-200323070-00005

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