Naunyn-Schmiedeberg's Archives of Pharmacology

, Volume 348, Issue 3, pp 332–337

Identification of P450 enzymes involved in metabolism of verapamil in humans

  • Heyo K. Kroemer
  • Jean-Charles Gautier
  • Philipe Beaune
  • Colin Henderson
  • C. Roland Wolf
  • Michel Eichelbaum
Article

DOI: 10.1007/BF00169164

Cite this article as:
Kroemer, H.K., Gautier, JC., Beaune, P. et al. Naunyn-Schmiedeberg's Arch Pharmacol (1993) 348: 332. doi:10.1007/BF00169164

Summary

The calcium channel blocker verapamil[2,8-bis-(3,4-dimethoxyphenyl)-6-methyl-2-isopropyl-6-azaoctanitrile] is widely used in the treatment of hypertension, angina pectoris and cardiac arrythmias. The drug undergoes extensive and variable hepatic metabolism in man with the major metabolic steps comprising formation of D-617 [2-(3,4-dimethoxyphenyl)-5-methylamino-2-isopropylvaleronitrile] and norverapamil [2,8-bis-(3,4-dimethoxyphenyl)-2-isopropyl-6-azaoxtanitrile]. The enzymes involved in metabolism of verapamil have not been characterized so far. Identification of these enzymes would enable estimation of both interindividual variability in verapamil metabolism introduced by the respective pathway and potential for metabolic interactions. We therefore characterized the enzymes involved in formation of D-617 and norverapamil.

The maximum rate of formation of D-617 and norverapamil was determined in the microsomal fraction of 21 human livers which had been previously characterized for the individual expression of various P450 enzymes (CYP1A2, CYP2C, CYP2D6, CYP2E1 and CYP3A3/4) by means of Western blotting. Specific antibodies directed against CYP3A were used to inhibit formation of D-617 and norverapamil. Finally, formation of both metabolites was investigated in microsomes obtained from yeast cells which were genetically engineered for stable expression of human P450.

Formation of D-617 was correlated with the expression of CYP3A (r=0.85; P<0.001) and CYP1A2 (r=0.57; P<0.01) in the microsomal fraction of 21 human livers after incubation with racemic verapamil. Formation of norverapamil was correlated with the expression of CYP3A (r=0.58; P<0.01) and CYP1A2 (r=0.5; P<0.05) in the same preparations after incubation with racemic verapamil. Antibodies against CYP3A reduced maximum rate of formation of D-617 (to 37.1±11% and 40.6±6.801o of control after incubation with S- and R-verapamil, respectively) and norverapamil (to 38.2±4.5% and 29.2±5.5% of control after incubation with S- and R-verapamil, respectively). Both D-617 and norverapamil were formed by stable expressed CYP3A4 (16.6 pmol/mg protein/min and 22.6 pmol/mg protein/min, respectively). In summary, formation of D-617 and norverapamil is catalyzed mainly by CYP3A4. D-617 is also formed by CYP1A2. Veraparnil therefore has the potential to interact with other drugs which are substrates or inducers of CYP3A and CYP1A2.

key words

Verapamil Metabolism Cytochrome P450 Human liver 

Copyright information

© Springer-Verlag 1993

Authors and Affiliations

  • Heyo K. Kroemer
    • 1
  • Jean-Charles Gautier
    • 2
  • Philipe Beaune
    • 2
  • Colin Henderson
    • 3
  • C. Roland Wolf
    • 3
  • Michel Eichelbaum
    • 1
  1. 1.Dr. Margarete Fischer-Bosch-Institut für Klinische PharmakologieStuttgartGermany
  2. 2.Inserm U75CHU Necker-Enfants-MaladesParisFrance
  3. 3.Biomedical Research CentreUniversity of DundeeDundeeUnited Kingdom

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