Evidence map›Paper›PMID 40885108›Full record

ArticleDrug metabolism and disposition: the biological fate of chemicals2025

Metabolic activation of flunitrazepam via nitroreduction mediated by aldo-keto reductase 1C3.

Cátia F Marques, Maya Narang, Kim A Sharp, Trevor M Penning

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Article in Drug metabolism and disposition: the biological fate of chemicals, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Cátia F MarquesDepartment of Systems Pharmacology & Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Maya NarangDepartment of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Kim A SharpDepartment of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Trevor M PenningDepartment of Systems Pharmacology & Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; Center of Excellence in Environmental Toxicology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania. Electronic address: penning@upenn.edu.

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI A. Clementina Mesaros · 2006 to 2026
$35.3M
Metabolic activation of nitroarenes and Nrf2-Keap1R01ES029294 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Trevor M Penning · 2019 to 2026
$3.6M
Computational Resource for Structural Biology and Molecular BiophysicsS10OD023592 · OD · UNIVERSITY OF PENNSYLVANIA · PI SHARP, KIM A · 2017 to 2017
$402k
NIEHS NIH HHS P30 ES013508NIEHS NIH HHS R01 ES029294NIH HHS S10 OD023592
6 · The paper itself

Abstract

Aldo-keto reductases (AKRs) are a superfamily of NAD(P)(H)-dependent oxidoreductases (phase I enzymes) that reduce aldehydes and ketones to primary and secondary alcohols, respectively. Four percent of xenobiotic biotransformation has been attributed to AKRs, although this is likely an underestimate because this is based on their ability to act as carbonyl reductases. AKRs also have an emerging role in nitroreduction. We screened 6 nitro-containing drugs (flunitrazepam, clonazepam, nimesulide, nilutamide, flutamide, and chloramphenicol) as substrates against recombinant human AKR1C1, AKR1C2, AKR1C3, and AKR1C4, using discontinuous enzymatic assays. AKR1C3 was able to reduce flunitrazepam to 7-amino-flunitrazepam. Metabolites formed during the reaction were identified by tandem mass spectrometry, which confirmed the formation of nitroso and hydroxylamino intermediates. The role of AKR1C3 was confirmed in HepG2 cells since AKR1C3-specific inhibitors blocked the formation of 7-amino-flunitrazepam. Interestingly, clonazepam (which lacks the tertiary amide of flunitrazepam) was not metabolized by AKR1C3. Molecular docking and dynamics simulations indicated that residue 120 (methionine) in AKR1C3 plays an important role in flunitrazepam-protein binding. Our computational approach suggested that the interaction between the flunitrazepam and AKR1C1, AKR1C2, and AKR1C4 is unlikely to occur and supported our experimental results. Our findings show that AKR1C3 can reduce flunitrazepam to reactive nitroso intermediates that could enhance drug toxicity and that flunitrazepam inhibits AKR1C2, which is responsible for the formation of the neuroactive steroid allopregnanolone. We conclude that both AKR1C3 and AKR1C2 may have an important role in flunitrazepam drug response. SIGNIFICANCE STATEMENT: Aldo-keto reductase (AKR)1C3 reduces flunitrazepam to 7-amino-flunitrazepam through the formation of reactive nitroso and hydroxylamino intermediates, and by inhibiting AKR1C2, flunitrazepam may reduce the formation of the neuroactive steroid allopregnanolone.

Indexed as

3-Hydroxysteroid DehydrogenasesFlunitrazepamHydroxyprostaglandin Dehydrogenases20-Hydroxysteroid Dehydrogenases3-alpha-Hydroxysteroid Dehydrogenase (B-Specific)Activation, MetabolicAldo-Keto Reductase Family 1 Member C3HumansMolecular Docking SimulationOxidation-Reduction20-Hydroxysteroid Dehydrogenases3 alpha-beta, 20 beta-hydroxysteroid dehydrogenase3-alpha-Hydroxysteroid Dehydrogenase (B-Specific)3-Hydroxysteroid DehydrogenasesAKR1C2 protein, humanAKR1C3 protein, humanAldo-Keto Reductase Family 1 Member C3FlunitrazepamHydroxyprostaglandin DehydrogenasesAldo-keto reductasesDrug metabolismHepatoma cellsMass spectrometry

Identifiers

PMID40885108
PMCPMC12562546

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.