Gut microbiota metabolizes nabumetone in vitro: Consequences for its bioavailability in vivo in the rodents with altered gut microbiome
Autor: | Hana Kozakova, Tomas Hudcovic, Milan Kolar, Eva Anzenbacherova, Petra Hermanova, Lenka Jourova, Jan Strojil, Zuzana Matuskova, Miloslav Kverka, Pavel Anzenbacher, Rostislav Vecera, Milan Nobilis |
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Rok vydání: | 2019 |
Předmět: |
Pharmacology
biology Chemistry medicine.drug_class Health Toxicology and Mutagenesis Antibiotics Cmax General Medicine Gut flora Toxicology biology.organism_classification 030226 pharmacology & pharmacy Biochemistry Bioavailability 03 medical and health sciences Nabumetone 0302 clinical medicine Pharmacokinetics In vivo 030220 oncology & carcinogenesis medicine Active metabolite medicine.drug |
Zdroj: | Xenobiotica. 49:1296-1302 |
ISSN: | 1366-5928 0049-8254 |
Popis: | 1. The underlying microbial metabolic activity toward xenobiotics is among the least explored factors contributing to the inter-individual variability in drug response. 2. Here, we analyzed the effect of microbiota on a non-steroidal anti-inflammatory drug nabumetone. 3. First, we cultivated the drug with the selected gut commensal and probiotic bacteria under both aerobic and anaerobic conditions and analyzed its metabolites by high-performance liquid chromatography (HPLC) with UV detection. To analyze the effect of microbiota on nabumetone pharmacokinetics in vivo, we administered a single oral dose of nabumetone to rodents with intentionally altered gut microbiome - either rats treated for three days with the antibiotic imipenem or to germ-free mice. Plasma levels of its main active metabolite 6 methoxy-2-naphthylacetic acid (6-MNA) were analyzed at pre-specified time intervals using HPLC with UV/fluorescence detection. 4. We found that nabumetone is metabolized by bacteria to its non-active metabolites and that this effect is stronger under anaerobic conditions. Although in vivo, none of the pharmacokinetic parameters of 6-MNA was significantly altered, there was a clear trend towards an increase of the AUC, Cmax and t1/2 in rats with reduced microbiota and germ-free mice. |
Databáze: | OpenAIRE |
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