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肠道微生物群代谢萘丁美酮:对肠道微生物群改变的啮齿动物其生物利用度的影响。

Gut microbiota metabolizes nabumetone : Consequences for its bioavailability in the rodents with altered gut microbiome.

作者信息

Jourova Lenka, Anzenbacher Pavel, Matuskova Zuzana, Vecera Rostislav, Strojil Jan, Kolar Milan, Nobilis Milan, Hermanova Petra, Hudcovic Tomas, Kozakova Hana, Kverka Miloslav, Anzenbacherova Eva

机构信息

a Department of Medical Chemistry and Biochemistry, Faculty of Medicine and Dentistry, Palacky University Olomouc , Czech Republic.

b Department of Pharmacology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc , Czech Republic.

出版信息

Xenobiotica. 2019 Nov;49(11):1296-1302. doi: 10.1080/00498254.2018.1558310. Epub 2019 Feb 22.

DOI:10.1080/00498254.2018.1558310
PMID:30794062
Abstract
  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 , 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 , none of the pharmacokinetic parameters of 6-MNA was significantly altered, there was a clear trend towards an increase of the AUC, Cmax and in rats with reduced microbiota and germ-free mice.
摘要
  1. 微生物对外源化合物的潜在代谢活性是导致个体间药物反应差异的最少被探索的因素之一。2. 在此,我们分析了微生物群对非甾体抗炎药萘丁美酮的影响。3. 首先,我们在需氧和厌氧条件下将该药物与选定的肠道共生菌和益生菌一起培养,并用高效液相色谱法(HPLC)结合紫外检测分析其代谢产物。为了分析微生物群对萘丁美酮药代动力学的影响,我们给肠道微生物群有意改变的啮齿动物单次口服萘丁美酮——用抗生素亚胺培南治疗三天的大鼠或无菌小鼠。使用HPLC结合紫外/荧光检测在预先设定的时间间隔分析其主要活性代谢产物6-甲氧基-2-萘乙酸(6-MNA)的血浆水平。4. 我们发现萘丁美酮被细菌代谢为其非活性代谢产物,并且这种作用在厌氧条件下更强。虽然6-MNA的药代动力学参数均未显著改变,但在微生物群减少的大鼠和无菌小鼠中,AUC、Cmax和有明显的升高趋势。

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