PT - JOURNAL ARTICLE AU - Taavitsainen, Päivi AU - Juvonen, Risto AU - Pelkonen, Olavi TI - In Vitro Inhibition of Cytochrome P450 Enzymes in Human Liver Microsomes by a Potent CYP2A6 inhibitor, <em>trans</em>-2-Phenylcyclopropylamine (Tranylcypromine), and Its Nonamine Analog, Cyclopropylbenzene DP - 2001 Mar 01 TA - Drug Metabolism and Disposition PG - 217--222 VI - 29 IP - 3 4099 - http://dmd.aspetjournals.org/content/29/3/217.short 4100 - http://dmd.aspetjournals.org/content/29/3/217.full SO - Drug Metab Dispos2001 Mar 01; 29 AB - Currently, there are no selective, well characterized inhibitors for CYP2A6. Therefore, the effects oftrans-(±)-2-phenylcyclopropylamine (tranylcypromine), a potent CYP2A6 inhibitor, on human liver microsomal cytochromes P450 (CYP) were studied to elucidate its selectivity. The IC50value of tranylcypromine in coumarin 7-hydroxylation (CYP2A6 model activity) was 0.42 ± 0.07 μM and in chlorzoxazone 6-hydroxylation (CYP2E1 model activity) 3.0 ± 1.1 μM. The IC50 values for CYP1A2, CYP2C9, CYP2C19, CYP2D6, and CYP3A4 activities were &gt;10 μM. Potency and selectivity of tranylcypromine were strongly dependent on the amine group, because its nonamine analog cyclopropylbenzene was much less potent inhibitor of CYP1A, CYP2A6, CYP2C19, and CYP2E1 activities and did not inhibit at all CYP2C9, CYP2D6, or CYP3A4 activities. In human liver microsomes tranylcypromine induced type II and cyclopropylbenzene type I difference spectrum. According to the double reciprocal analysis of these spectral responses both tranylcypromine and cyclopropylbenzene may have at least two P450-related binding sites in liver microsomes. TheKa values of tranylcypromine varied from 4.5 to 15.1 μM and −34.3 to 167 μM in microsomes derived from three different livers and of cyclopropylbenzene from −1.6 to 10.1 μM and −34.6 and 75.2 μM in the same liver microsomes. Based on these results, tranylcypromine seems an adequately selective CYP2A6 inhibitor for in vitro use. The American Society for Pharmacology and Experimental Therapeutics