Skip to main content
Log in

Induction of drug metabolism in man after rifampicin treatment measured by increased hexobarbital and tolbutamide clearance

  • Published:
European Journal of Clinical Pharmacology Aims and scope Submit manuscript

Summary

Five healthy volunteers took 1.2 g rifampicin daily for 8 days, and before and afterwards each received hexobarbital (7.32 mg/kg) and tolbutamide (20 mg/kg) by i.v. infusion on two consecutive days. The plasma concentrations of the two drugs were determined during and after infusion. The average elimination half-life of hexobarbital had decreased from 325 to 122 min and of tolbutamide from 418 to 183 min following rifampicin treatment. It was calculated that the metabolic clearance of hexobarbital had increased about three-fold and that of tolbutamide more than two-fold. Significant changes in the distribution kinetics of the two drugs were not observed. The results suggest that rifampicin is capable of inducing drug metabolism in man, which leads to an increased rate of elimination of drugs that undergo biotransformation in the liver.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  • Acocella, G., L. Bonollo, M. Garimoldi, M. Mainardi, T. Tenconi, F.B. Nicolis: Kinetics of rifampicin and isoniazid administered alone and in combination to normal subjects and patients with liver disease. Gut13, 47–53 (1972a)

    Google Scholar 

  • Acocella, G., A. Lamarina, F.B. Nicolis, V. Pagani, G. Segre: Kinetic studies on rifampicin. II. Multicompartmental analysis of the serum, urine and bile concentrations in subjects treated for one week. Europ. J. clin. Pharmacol.5, 111–115 (1972b)

    Google Scholar 

  • Boman, G.: Serum concentration and half-life of rifampicin after simultaneous oral administration of aminosalicylic acid or isoniazid. Europ. J. clin. Pharmacol.7, 217–225 (1974)

    Google Scholar 

  • Bradley, S.E., F.J. Ingelfinger, G.P. Bradley: Hepatic circulation in cirrhosis of the liver. Circulation5, 419–429 (1952)

    Google Scholar 

  • Branch, A.R., G.D. Shand, G.R. Wilkinson, A.S. Nies: Increased clearance of antipyrine and d-propranolol after phenobarbital treatment in the monkey. J. clin. Invest.53, 1101–1107 (1974)

    Google Scholar 

  • Breimer, D.D.: Pharmacokinetics and biopharmaceutics of barbiturates and chloral hydrate in man. Ph.D.-thesis, Nijmegen, The Netherlands, (1974)

  • Breimer, D.D., J.M. van Rossum: Rapid and sensitive gas chromatographic determination of hexobarbital in plasma of man using a nitrogen detector. J. Chromatogr.88, 235–243 (1974)

    Google Scholar 

  • Breimer, D.D., C. Honhoff, W. Zilly, E. Richter, J.M. van Rossum: Pharmacokinetics of hexobarbital in man after intravenous infusion. J. Pharmacokin. Biopharm.3, 1–11 (1975)

    Google Scholar 

  • Bush, M.T., W.L. Weller: Metabolic fate of hexobarbital (HB). Drug Metab. Rev.1, 249–290 (1972)

    Google Scholar 

  • Bush, M.T., T.C. Butler, H.L. Dickison: The metabolic fate of 5(1 - cyclo-hexen-1-yl)-1,5-dimethyl barbituric acid (hexobarbital, Evipal) and of 5-(1-cyclo-hexen-1-yl)-5-methyl barbituric acid (“Nor-Evipal”). J. Pharmacol. exp. Ther.108, 104–111 (1953)

    Google Scholar 

  • Curci, G., N. Bergamini, F. Delli Veneri, A. Ninni, V. Nitti: Half-life of rifampicin after repeated administration of different doses in humans. Chemotherapia (Basel)17, 373–381 (1972)

    Google Scholar 

  • Edwards, O.M., R.J. Cortenay-Evans, J.M. Galley, J. Hunter, A.D. Tait: Changes in cortisol metabolism following rifampicin therapy. Lancet1974 II, 549–551

    Google Scholar 

  • Freij, H.H., F. Sudeney, D. Kranse: Vergleichende Untersuchungen über Stoffwechsel, Ausscheidung und Nachweis von Schlafmitteln aus der Barbitursäurereihe. Arzneimittel-Forsch.9, 294–297 (1959)

    Google Scholar 

  • Gillette, J.R.: Factors affecting drug metabolism. In: Drug metabolism in man. Ann. N.Y. Acad. Sci.179, 43–66 (1971)

    Google Scholar 

  • Hakim, J., G. Feldmann, J. Bucherot, P. Boivin, P. Guibout, B. Kreis: Effect of rifampicin, isoniazid and streptomycin on the human liver: a problem of enzyme induction. Gut12, 761 (1971)

    Google Scholar 

  • Held, H., R. Eisert, H.F. von Oldershausen: Pharmakokinetik von Glymidine (Glycodiazin) und Tolbutamid bei akuten und chronischen Leberschäden. Arzneimittel-Forsch. (Drug Res.)23, 1801–1807 (1973)

    Google Scholar 

  • Jezequel, A.M., F. Orlandi, L.T. Tenconi: Changes of the smooth endoplasmic reticulum induced by rifampicin in human and guineapig hepatocytes. Gut12, 984–987 (1971)

    Google Scholar 

  • Loo, J.C.K., S. Riegelman: Assessment of pharmacokinetic constants from postinfusion blood curves obtained after i.v. infusion. J. pharm. Sci.59, 53–55 (1970)

    Google Scholar 

  • Maggi, N., S. Furesz, R. Pallanza, G. Pelizza: Rifampicin desacetylation in the human organism. Arzneimittel-Forsch.19, 651–654 (1969)

    Google Scholar 

  • Melikian, V., J.D. Eddy, A. Paton: The stimulant effect of drugs on indocyanine green clearance by the liver. Gut13, 755–758 (1972)

    Google Scholar 

  • Michot, F., M. Bürgi, J. Büttner: Rimactan (Rifampicin) und Antikoagulantientherapie. Schweiz. med. Wschr.100, 583–587 (1970)

    Google Scholar 

  • Nelson, E., J. O'Reilly, Th. Chulski: Determination of carboxytolbutamide in urine. Clin. chim. Acta5, 774–776 (1960)

    Google Scholar 

  • Nocke-Fink, L., H. Breuer, D. Reimers: Wirkung von Rifampicin auf den Menstruationszyklus und die Östrogenausscheidung bei Einnahme oraler Kontrazeptiva. Dtsch. med. Wschr.98, 1521–1523 (1973)

    Google Scholar 

  • Remmer, H., B. Schoene, R. Fleischmann, H. Held: Induction of the unspecific microsomal hydroxylase in the human liver. In: The liver. Quantitative aspects of structure and function. p. 232, Basel: Karger 1973

    Google Scholar 

  • Riegelman, S., M. Rowland: Effect of route of administration on drug disposition. J. Pharmacokin. Biopharm.1, 419–434 (1973)

    Google Scholar 

  • Rossum, J.M. van: Significance of pharmacokinetics for drug design and the planning of dosage regimes. In: Drug design, vol. I, pp. 469–521, New York: Academic Press, 1971

    Google Scholar 

  • Rowland, M., L.Z. Benet, G.G. Graham: Clearance concepts in pharmacokinetics. J. Pharmacokin. Biopharm.1, 123–136 (1973)

    Google Scholar 

  • Scheuer, P.J., S. Lal, J.A. Summerfield, S. Sherlock: Rifampicin hepatitis. Lancet1974 I, 421–425

    Google Scholar 

  • Schoene, B., R.A. Fleischmann, H. Remmer, H.F. von Oldershausen: Determination of drug metabolizing enzymes in needle biopsies of human liver. Europ. J. clin. Pharmacol.4, 65–73 (1973)

    Google Scholar 

  • Scholtan, W.: Die Bindung der Sulfonamide an Eiweißkörper. 6. Bestimmung der Eiweißbindung von Sulfonamiden mittels der Ultrazentrifuge und mittels Gelfiltration. Arzneimittel-Forsch.15, 1433–1441 (1965)

    Google Scholar 

  • Spingler, H.: Über eine Möglichkeit zur colorimetrischen Bestimmung von N-(4-Methyl-benzolsulfonyl)-N'-butyl-Harnstoff in Serum. Klin. Wschr.10, 533–535 (1957)

    Google Scholar 

  • Südhof, H., W. Eger, S. Altenburg, G. Schumacher: Blutzuckersenkung durch orale Antidiabetica und Verhalten des N-(4-Methyl-benzolsulfonyl)-N'-butyl-Harnstoffes im Serum in Abhängigkeit von der Leberfunktion. Arzneimittel-Forsch. (Drug Res.)7, 438–442 (1958)

    Google Scholar 

  • Thomas, R.C., G.J. Ikeda: The metabolic fate of tolbutamide in man and in the rat. J. med. Chem.9, 507–518 (1966)

    Google Scholar 

  • Thomson, P.D., K.L. Melman, J.A. Richardson, K. Cohn, W. Steinbrunn, R. Cudihee, M. Rowland: Lidocaine pharmacokinetics in advanced heart failure, liver disease and renal failure in humans. Ann int. Med.78, 499–508 (1973)

    Google Scholar 

  • Tsukamoto, H., S. Toki, K. Kaneda: Detection of hydroxyl derivatives from urine of men administered ethyl-hexabital and methyl-hexabital by buffered paper chromatography. Chem. pharm. Bull.6, 625–626 (1957)

    Google Scholar 

  • Virtanen, S., E. Tala: Serum concentration of rifampicin after oral administration. Clin. Pharmacol. Ther.16, 817–820 (1974)

    Google Scholar 

  • Zilly, W., D.D. Breimer, E. Richter: Unpublished investigation.

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zilly, W., Breimer, D.D. & Richter, E. Induction of drug metabolism in man after rifampicin treatment measured by increased hexobarbital and tolbutamide clearance. Eur J Clin Pharmacol 9, 219–227 (1975). https://doi.org/10.1007/BF00614021

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00614021

Key words

Navigation