Allosteric activation of cytochrome P450 3A4 by efavirenz facilitates midazolam binding. (2nd December 2018)

• Record Type: Journal Article
• Authors: Ichikawa, Tomohiko; Tsujino, Hirofumi; Miki, Takahiro; Kobayashi, Masaya; Matsubara, Chiaki; Miyata, Sara; Yamashita, Taku; Takeshita, Kohei; Yonezawa, Yasushige; Uno, Tadayuki
• Is Part Of: Xenobiotica. Volume 48:Number 12(2018:Dec.)
• Page Start: 1227
• Page End: 1236
• Publication Date: 2018-12-02
• Subjects: Cytochrome P450 3A4 -- drug–drug interaction -- efavirenz -- midazolam; Metabolism -- Periodicals; Drugs -- Physiological effect -- Periodicals; Food additives -- Periodicals; Chemicals -- Physiological effect -- Periodicals; Biochemistry -- Periodicals; Pharmaceutical Preparations -- metabolism -- Periodicals; Metabolism -- Periodicals; 574.133
• DOI: 10.1080/00498254.2017.1412540
• Languages: English
• ISSNs: 0049-8254

Abstract

Abstract: 1. The purpose of this study is to investigate the heteroactivation mechanism of CYP3A4 by efavirenz, which enhances metabolism of midazolam in vivo, in terms of its binding to CYP3A4 with in vitro spectroscopic methods. 2. Efavirenz exhibited a type II spectral change with binding to CYP3A4 indicating a possible inhibitor. Although dissociation constant ( K d ) was approximated as 520 μM, efavirenz enhanced binding affinity of midazolam as a co-existing drug with an estimated i K d value of 5.6 µM which is comparable to a clinical concentration. 3. Efavirenz stimulated the formation of 1′-hydroxymidazolam, and the product formation rate ( V max ) concentration-dependently increased without changing the K m . Besides, an efavirenz analogue, [6-chloro-1, 4-dihydro-4-(1-pentynyl)-4-(trifluoromethyl)-2H-3, 1-benzoxazin-2-one] (efavirenz impurity) slightly facilitated the binding affinity of midazolam in a concentration-dependent manner. These results propose that efavirenz affects midazolam-binding via binding to the peripheral site which is apart from the active site of CYP3A4. 4. A molecular dynamics simulation also suggested the bound-efavirenz was repositioned to effector-binding site. As a consequence, our spectroscopic studies clarified the heteroactivation of CYP3A4 caused by efavirenz with a proper affinity to the peripheral site, and we concluded the method can be a useful tool for characterising the potential for drug–drug interactions.