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Involvement of CYP1A2 in mexiletine metabolism
Author(s) -
Nakajima M.,
Kobayashi K.,
Shimada N.,
Tokudome S.,
Yamamoto T.,
Kuroiwa Y.
Publication year - 1998
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1046/j.1365-2125.1998.00048.x
Subject(s) - mexiletine , cyp1a2 , microsome , cyp2d6 , metabolism , theophylline , pharmacology , chemistry , cytochrome p450 , quinidine , biochemistry , enzyme , medicine , biology
Aims Mexiletine has been reported to be hydroxylated by cytochrome P450 2D6 (CYP2D6) in humans. However, the involvement of CYP1A2 in the metabolism of mexiletine has been proposed based on the interaction with theophylline which is mainly metabolized by CYP1A2. The aim of this study was to clarify the role of human CYP1A2 in mexiletine metabolism.Methods Human CYP isoforms involved in mexiletine metabolism were investigated using microsomes from human liver and B‐lymphoblastoid cells expressing human CYPs. The contributions of CYP1A2 and CYP2D6 to mexiletine metabolism were estimated by the relative activity factor (RAF).Results Mexiletine p ‐ and 2‐hydroxylase activities in human liver microsomes were inhibited by ethoxyresorufin and furafylline as well as quinidine. Mexiletine p ‐ and 2‐hydroxylase activities in microsomes from nine human livers correlated significantly with bufuralol 1′‐hydroxylase activity ( r =0.907, P <0.001 and r =0.886, P <0.01, respectively). Microsomes of B‐lymphoblastoid cells expressing human CYP1A2 exhibited lower mexiletine p ‐ and 2‐hydroxylase activities than those expressing human CYP2D6. It was estimated by RAF that the major isoform involved in mexiletine metabolism was CYP2D6, and the contribution of CYP1A2 to both mexiletine p ‐ and 2‐hydroxylase activities was 7–30% in human liver microsomes. However, the K m values of the expressed CYP1A2 (∼15 μm ) were almost identical with those of the expressed CYP2D6 (∼22 μm ) and human liver microsomes.Conclusions Mexiletine is a substrate of CYP1A2. The data obtained in this study suggest that the interaction of mexiletine with theophylline might be due to competitive inhibition of CYP1A2.