Skip to main content
Log in

The influence of dimethylbiguanide on phenprocoumon elimination and its mode of action

A drug interaction study

  • Originalien
  • Published:
Klinische Wochenschrift Aims and scope Submit manuscript

Summary

This study was based on the clinical observation of a higher phenprocoumon requirement in these diabetic patients simultaneously treated with phenprocoumon (MarcoumarR) and dimethylbiguanide (DMB), and of a drug interaction observed in a patient. These higher requirements of phenprocoumon, suggesting an increased elimination, could have been due to an enhancement of liver microsomal enzyme activity and/or an increase in liver blood flow. Various studies were performed to test this hypothesis. The clinically suggested higher phenprocoumon requirement was proven by a drug observation study. Hence a higher tablet consumption of phenprocoumon and a diminished anticoagulatory effect was found after treatment with DMB in doses of between 1 and 3 g. An increased elimination of phenprocoumon following DMB administration was also found in a pharmacokinetic study. The activity of the liver microsomal enzyme system, investigated in animal and man, showed no changes in the liver microsomal enzymes in animal studies or the in vivo parameters of liver microsomal enzyme activity in patients. Measuring liver blood flow in dogs, utilizing the indocyanine green clearance method, an increased flow of about 33% was observed. As changes in liver blood flow can increase the metabolism of some highly lipid soluble drugs, the increased metabolism of phenprocoumon during DMB treatment could be related to the increase in liver blood flow and not to changes in liver microsomal enzyme activity. In addition, DMB could inhibit the known enterohepatic circulation of phenprocoumon and so increase phenprocoumon elimination. Therefore, careful monitoring of the pharmacodynamic effect should be performed in those patients treated with a combination of phenprocoumon and DMB.

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.

Similar content being viewed by others

References

  1. Aggeler PM, O'Reilly RA (1969) Effect of heptabarbital on the response to bishydroxycoumarin in man. J Lab Clin Med 74:229–238

    PubMed  Google Scholar 

  2. Assan R, Heuclin Ch, Ganeval G, Bismuth Ch, George J, Girard JP (1977) Metformin induced lactic acidosis in the presence of acute renal failure. Diabetologica 13:211–217

    Google Scholar 

  3. Beckmann R (1971) Oral wirksame Antidiabetika. In: Beckmann (ed) Handbook of Experimental Pharmacology. Vol. 29. Springer Verlag, Heidelberg, New York, pp 45–46

    Google Scholar 

  4. Bergmann U, Boman G, Wiholm BE (1978) Epidemiology of adverse drug reactions to phenformin and metformin. Br Med J, pp 464–466

  5. Branch RA, Shand DG, Wilkinson GR, Nies AS (1974) Increased clearance of antipyrine and d-propranolol after phenobarbital treatment in the monkey. Relative contributions of enzyme induction and increased hepatic blood flow. J Clin Invest 53:1101–1107

    PubMed  Google Scholar 

  6. Breckenridge A, Orme M L'e, Thorgeirsson S, Davies DS, Brooks RV (1971) Drug interactions with warfarin: Studies with dichloralphenazone, chloral hydrate and phenazone (antipyrine). Clin Sci 40:351–364

    PubMed  Google Scholar 

  7. British Medical Journal (1977) Editorial: Biguanides and lactic acidosis in diabetics. Br Med J 2:1436

    Google Scholar 

  8. Brodie BB, Axelrod J, Soberman R, Levy BB (1949) The estimation of antipyrine in biological materials. J Biol Chem 179:25–29

    Google Scholar 

  9. Caesar J, Shaldon S, Chiandussi L, Guevara L, Sherlock S (1961) The use of indocyanine green in the measurement of hepatic blood flow and as a test of hepatic function. Clin Sci 21:43–57

    PubMed  Google Scholar 

  10. Debry G, Laurent J (1970) Acidose lactique et diabète sucré. Helv Med Acta 35:433–447

    PubMed  Google Scholar 

  11. George ChF (1980) Drug kinetics and hepatic blood flow. Clin. Pharmacokinet 4:433–448

    Google Scholar 

  12. Gyr N, Berger W, Fridrich A, Denes A, Stalder GA (1971) Der Einfluß von Dimethylbiguanid auf die Magenentleerung und die orale Glukosetoleranz. Schweiz Med Wochenschr 101:1876–1879

    PubMed  Google Scholar 

  13. Heni N, Glogner P (1976) Pharmacokinetics of phenprocoumon in man investigated using a gas chromatographic method of drug analysis. Naunyn Schmiedebergs Arch Pharmacol 293:183–186

    PubMed  Google Scholar 

  14. Jähnchen E, Meinertz Th, Gilfrich HJ, Groth U, Martini A (1976) The enantiomers of phenprocoumon: pharmacodynamic and pharmacokinetic studies. Clin Pharmacol Ther 20:342–349

    PubMed  Google Scholar 

  15. Kitteringham N, Büstgens L, Brundert E, Mineshita S, Ohnhaus EE (1983) Pharmacokinetics of phenprocoumon in patients with liver cirrhosis. Br J Clin Pharmacol 15:590 p

    Google Scholar 

  16. Koch-Weser J, Sellers EM (1971) Drug interactions with coumarin anticoagulants. N Engl Med 285:487–498

    Google Scholar 

  17. Koch-Weser J, Sellers EM (1976) Binding of drugs to serum albumin. N Engl J Med 294:526–531

    PubMed  Google Scholar 

  18. Lebacq EG, Tirzmalis A (1973) Metformin and lactic acidosis. Lancet i:314

    Google Scholar 

  19. Luft D, Schmulling RM, Eggstein M (1978) Lactic acidosis in biguanide-treated diabetes. Diabetologia 14:75–87

    PubMed  Google Scholar 

  20. March J, Turner WJ, Shanley J, Field J (1974) Values for urinary excretion of d-glucaric acid by normal individuals. Clin Chem 20:1155–1158

    PubMed  Google Scholar 

  21. Meinertz Th, Gilfrich HJ, Groth U, Jonen HG, Jähnchen E (1977) Interruption of the enterohepatic circulation of phenprocoumon by cholestyramine. Clin Pharmacol Ther 21:731–735

    PubMed  Google Scholar 

  22. Oesch E, Jerina DM, Daly J (1971) A radiometric assay for hepatic epoxide hydrase activity with (7-3H) styrene oxide. J Biochem Biophys Acta 227:685–691

    Google Scholar 

  23. Oesch F, Ohnhaus EE (1974) Dimethylbiguanide-evoked increase of anticoagulant elimination not associated with induction of drug metabolizing enzymes. Biochem Med 11:344–349

    PubMed  Google Scholar 

  24. Ohnhaus EE, Thorgeirsson SS, Davies DS, Breckenridge A (1971) Changes in liver blood flow during enzyme induction. Biochem Pharmacol 20:2561–2570

    PubMed  Google Scholar 

  25. Ohnhaus EE, Berger W (1975) The influence of dimethylbiguanide (DMB) on liver blood flow in dogs. Diabetologia 11:367

    Google Scholar 

  26. Ohnhaus EE, Martin J, Kinser J, Colombo JP (1977) Enzyme induction and renal function in man. Br J Clin Pharmacol 4:33–37

    PubMed  Google Scholar 

  27. Ohnhaus EE, Berger W, Nars PW (1978) The effect of different doses of dimethyl-biguanide (DMB) on liver blood flow, blood glucose and plasma immunoreactive insulin in anaesthetized rats. Biochem Pharmacol 27:789–793

    PubMed  Google Scholar 

  28. Ohnhaus EE, Park BK (1979) Measurement of urinary 6-β-hydroxycortisol excretion as an in vivo parameter in the clinical assessment of the microsomal enzyme-inducing capacity of antipyrine, phenobarbitone and rifampicin. Eur J Clin Pharmacol 15:139–145

    PubMed  Google Scholar 

  29. Ohnhaus EE (1979) Arzneimittelwirkungen durch Beeinflussung der Plasmaciweißbindung. Internist 20:225–228

    PubMed  Google Scholar 

  30. Omura T, Sato R (1964) The carbon monoxide-binding pigment. J Biol Chem 239:2370–2378

    PubMed  Google Scholar 

  31. Park BK (1978) A direct radioimmunoassay for 6-β-hydroxycortisol in human urine. J Steroid Biochem 9:963–966

    PubMed  Google Scholar 

  32. Pentikäinen PJ, Neuvonen PJ, Penttilä A (1979) Pharmacokinetics of metformin after intravenous and oral administration to man. Eur J Clin Pharmacol 16:195–202

    PubMed  Google Scholar 

  33. Phillips PJ, Thomas DW, Harding BE (1977) Biguanides and lactic acidosis in diabetics. Br Med J 2:1436

    Google Scholar 

  34. Poland AP, Nebert DM (1973) A sensitive radiometric assay of aminopyrine N-demethylation. J Pharmacol Exp Ther 184:269–277

    PubMed  Google Scholar 

  35. Sachs L (1978) Statistische Auswertungsmethoden. Springer Berlin Heidelberg New York

    Google Scholar 

  36. Seiler K, Duckert F (1968) Properties of 3-(1-Phenyl-Propyl)-4-oxycoumarin (Marcoumar) in the plasma when tested in normal cases and under the influence of drugs. Thromb Diath Haemorrhag 19:389–396

    Google Scholar 

  37. Shenfield GM, Bhalla IP, Steel JM, Duncan LJP (1977) Metformin in the treatment of obese diabetics. The Practitioner 219:745–749

    PubMed  Google Scholar 

  38. Sirtori CR, Francheschini G, Galli-Kienle M, Cighetti G, Galli G, Bondioli A, Conti F (1978) Disposition of metformin (N, N-dimethylbiguanide) in man. Clin Pharmacol Ther 24:683–693

    PubMed  Google Scholar 

  39. Sterne J (1974) The present state of knowledge on the model of action of the antidiabetic biguanides. Metabolism 13:791–798

    Google Scholar 

  40. Tucker GT, Casey C, Phillips PJ, Connor H, Ward JD, Woods HF (1981) Metformin kinetics in healthy subjects and in patients with diabetes mellitus. Br J Clin Pharmacol 12:235–246

    PubMed  Google Scholar 

  41. Walker RS, Linton AL (1959) Phenethyldiguanide: a dangerous side-effect. Br Med J 2:464–466

    Google Scholar 

  42. Wilkinson GR, Shand DG (1975) A physiological approach to hepatic drug clearance. Clin Pharmacol Ther 18:377–390

    PubMed  Google Scholar 

  43. Wilkinson GR, Schenker S (1976) Effects of liver disease on drug disposition in man. Biochem Pharmacol 25:2675–2681

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This study was supported by the “Schweizerische National Fonds” (Grant No. 348670)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ohnhaus, E.E., Berger, W., Duckert, F. et al. The influence of dimethylbiguanide on phenprocoumon elimination and its mode of action. Klin Wochenschr 61, 851–858 (1983). https://doi.org/10.1007/BF01537460

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01537460

Key words

Navigation