Department of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine and Hospital, Seoul, Korea.
Department of Medicine, Division of Infectious Diseases, Washington University School of Medicine, St. Louis, Missouri, USA.
Clin Transl Sci. 2020 Jul;13(4):752-760. doi: 10.1111/cts.12761. Epub 2020 Mar 29.
The pharmacokinetic (PK) properties of drugs are affected in several ways by interactions with microbiota. The aim of this study was to investigate the effects of oral vancomycin on the gut microbiota and, consequently, on the PKs of simvastatin. An open-label, single arm, sequential crossover study was conducted in six healthy Korean male subjects. After 6 days on a control diet, simvastatin 40 mg was orally administered to the subjects before and after 1 week of oral vancomycin treatment. Blood samples for PK analysis and fecal samples for metagenomic and metabolomic analyses were collected. After vancomycin treatment, the richness of microbiota considerably decreased, and the composition was altered. In particular, the relative abundance of Bacteroidetes decreased, whereas that of proteobacteria increased. In addition, changes in fecal metabolites, including D-glucuronic acid, were observed. However, systemic exposure of simvastatin was not changed whereas that of hydroxysimvastatin showed a tendency to increase. The relationship between the change of PKs of simvastatin and the change of gut microbiota and fecal metabolites were not clearly observed.
药物的药代动力学(PK)特性会受到与微生物群相互作用的多种方式的影响。本研究旨在研究口服万古霉素对肠道微生物群的影响,以及对辛伐他汀 PK 的影响。在 6 名健康韩国男性受试者中进行了一项开放标签、单臂、顺序交叉研究。在对照饮食 6 天后,在口服万古霉素治疗前和治疗后 1 周,口服辛伐他汀 40mg。采集用于 PK 分析的血样和用于宏基因组和代谢组学分析的粪便样。万古霉素治疗后,微生物群的丰富度显著降低,组成发生改变。特别是,拟杆菌门的相对丰度降低,而变形菌门的相对丰度增加。此外,还观察到粪便代谢物(包括 D-葡萄糖醛酸)的变化。然而,辛伐他汀的全身暴露没有改变,而羟基辛伐他汀的暴露则有增加的趋势。辛伐他汀 PK 变化与肠道微生物群和粪便代谢物变化之间的关系尚未清楚观察到。