Literature DB >> 20080160

Benzodiazepines medazepam and midazolam are activators of pregnane X receptor and weak inducers of CYP3A4: investigation in primary cultures of human hepatocytes and hepatocarcinoma cell lines.

Radim Vrzal1, Katerina Kubesova, Petr Pavek, Zdenek Dvorak.   

Abstract

Benzodiazepines have wide-spread used in pharmacotherapy for their anxiolytic, myorelaxant, hypnotic, amnesic and anticonvulsive properties. Despite benzodiazepines are used in clinics over 50 years, they have not been surprisingly tested for capability to induce major drug-metabolizing cytochromes P450. In the current study, we have examined the potency of Alprazolam, Bromazepam, Chlordiazepoxide, Clonazepam, Diazepam, Lorazepam, Medazepam, Midazolam, Nitrazepam, Oxazepam, Tetrazepam and Triazolam to induce CYP1A2 and CYP3A4 in primary cultures of human hepatocytes. Benzodiazepines were tested in therapeutic concentrations and in concentrations corresponding to their plasma levels in intoxicated patients. We found weak but significant induction of CYP3A4 mRNA by Midazolam and Medazepam, while other benzodiazepines did not induce CYP3A4 expression. None of the tested compounds induced CYP1A2 mRNA in three independent human hepatocytes cultures. In addition, employing gene reporter assays with transiently transfected hepatocarcinoma cells, we found that tested benzodiazepines did not activate aryl hydrocarbon receptor (AhR), whereas Midazolam and Medazepam slightly activated pregnane X receptor (PXR). Consistently, two-hybrid mammalian assay using hybrid fusion plasmids GAL4-PXR ligand-binding domain (LBD) and VP16-SRC-1-receptor-interacting domain (RID) confirmed PXR activation by Midazolam and Medazepam. In conclusion, Alprazolam, Bromazepam, Chlordiazepoxide, Clonazepam, Diazepam, Lorazepam, Nitrazepam, Oxazepam, Tetrazepam and Triazolam can be considered as safe drugs in term of their inability to induce PXR- and AhR-dependent cytochrome P450 enzymes CYP1A2 and CYP3A4. Medazepam and Midazolam slightly activated pregnane X receptor and displayed weak potency to induce CYP3A4 mRNA in human hepatocytes. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20080160     DOI: 10.1016/j.toxlet.2010.01.004

Source DB:  PubMed          Journal:  Toxicol Lett        ISSN: 0378-4274            Impact factor:   4.372


  5 in total

1.  Independent predictors of delay in emergence from general anesthesia.

Authors:  Shigeru Maeda; Yumiko Tomoyasu; Hitoshi Higuchi; Minako Ishii-Maruhama; Masahiko Egusa; Takuya Miyawaki
Journal:  Anesth Prog       Date:  2015

2.  Compensatory changes in CYP expression in three different toxicology mouse models: CAR-null, Cyp3a-null, and Cyp2b9/10/13-null mice.

Authors:  Ramiya Kumar; Linda C Mota; Elizabeth J Litoff; John P Rooney; W Tyler Boswell; Elliott Courter; Charles M Henderson; Juan P Hernandez; J Christopher Corton; David D Moore; William S Baldwin
Journal:  PLoS One       Date:  2017-03-28       Impact factor: 3.240

3.  Diazepam Promotes Translocation of Human Constitutive Androstane Receptor (CAR) via Direct Interaction with the Ligand-Binding Domain.

Authors:  Josef Skoda; Jan Dusek; Martin Drastik; Alzbeta Stefela; Klara Dohnalova; Karel Chalupsky; Tomas Smutny; Stanislav Micuda; Sabine Gerbal-Chaloin; Petr Pavek
Journal:  Cells       Date:  2020-11-24       Impact factor: 6.600

Review 4.  Regulation of PXR Function by Coactivator and Corepressor Proteins: Ligand Binding Is Just the Beginning.

Authors:  Juan Pablo Rigalli; Dirk Theile; Julie Nilles; Johanna Weiss
Journal:  Cells       Date:  2021-11-12       Impact factor: 6.600

5.  CYP2B6 allelic variants and non-genetic factors influence CYP2B6 enzyme function.

Authors:  Katalin Mangó; Ádám Ferenc Kiss; Ferenc Fekete; Réka Erdős; Katalin Monostory
Journal:  Sci Rep       Date:  2022-02-22       Impact factor: 4.379

  5 in total

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