کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2478965 1113414 2014 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Mechanism-based Inactivation of Cytochrome P450 2A6 and 2A13 by Rhinacanthus nasutus Constituents
موضوعات مرتبط
علوم پزشکی و سلامت داروسازی، سم شناسی و علوم دارویی اکتشاف دارویی
پیش نمایش صفحه اول مقاله
Mechanism-based Inactivation of Cytochrome P450 2A6 and 2A13 by Rhinacanthus nasutus Constituents
چکیده انگلیسی

Summary:Human cytochrome P450 CYP2A6 and CYP2A13 catalyze nicotine metabolisms and mediate activation of tobacco-specific carcinogens including 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL). In this study, we found rhinacanthins A, B, and C isolated from Rhinacanthus nasutus potentially inhibited coumarin 7-hydroxylation mediated by reconstituted purified recombinant CYP2A6 and CYP2A13. Rhinacanthins A-C are mechanism-based inactivators of CYP2A6 and CYP2A13 as they cause concentration, time and NADPH-dependent inhibition. Among the three rhinacanthins, rhinacanthin-B possessed highest inhibitory potency against CYP2A13 with apparent K and fcinact of 0.16 μΜ and 0.1 min− 1, respectively, while values of 0.44 μΜ and 0.12 min− 1 were found against CYP2A6. Rhinacanthin-C had least inhibition potency, with apparent K1 and kinact of 0.97 μΜ and 0.07 min− 1 for CYP2A6, respectively, and values of 1.68μΜ and 0.05 min− 1 for CYP2A13. Rhinacanthin-A inhibited CYP2A6 and CYP2A13 with apparent K1 values of 0.69 and 0.42 μΜ, respectively and apparent kinact of 0.18 and 0.06 min− 1, respectively. The inhibition of both enzymes by rhinacanthins A-C could not be prevented by addition of trapping agents or reversed by dialysis or potassium ferricyanide. These findings demonstrated that rhinacanthins A-C, which are 1,4-naphthoquinone derivatives, irreversibly inhibited CYP2A6 and CYP2A13 in a mechanism-based inhibition mode.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Drug Metabolism and Pharmacokinetics - Volume 29, Issue 1, 2014, Pages 75–82
نویسندگان
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