Division of Toxicology, Wageningen University and Research, Stippeneng 4, 6708 WE, Wageningen, The Netherlands.
BASF SE, 67056, Ludwigshafen, Germany.
Arch Toxicol. 2022 Dec;96(12):3291-3303. doi: 10.1007/s00204-022-03373-4. Epub 2022 Sep 8.
Bile acid homeostasis plays an important role in many biological activities through the bile-liver-gut axis. In this study, two in vitro models were applied to further elucidate the mode of action underlying reported in vivo bile acid changes induced by antibiotics (colistin sulfate, tobramycin, meropenem trihydrate, and doripenem hydrate). 16S rRNA analysis of rat fecal samples anaerobically incubated with these antibiotics showed that especially tobramycin induced changes in the gut microbiota. Furthermore, tobramycin was shown to inhibit the microbial deconjugation of taurocholic acid (TCA) and the transport of TCA over an in vitro Caco-2 cell layer used as a model to mimic intestinal bile acid reuptake. The effects induced by the antibiotics in the in vitro model systems provide novel and complementary insight explaining the effects of the antibiotics on microbiota and fecal bile acid levels upon 28-day in vivo treatment of rats. In particular, our results provide insight in the mode(s) of action underlying the increased levels of TCA in the feces upon tobramycin exposure. Altogether, the results of the present study provide a proof-of-principle on how in vitro models can be used to elucidate in vivo effects on bile acid homeostasis, and to obtain insight in the mode(s) of action underlying the effect of an antibiotic, in this case tobramycin, on bile acid homeostasis via effects on intestinal bile acid metabolism and reuptake.
胆汁酸稳态通过胆-肝-肠轴在许多生物活性中发挥重要作用。在这项研究中,应用了两种体外模型来进一步阐明抗生素(硫酸粘菌素、妥布霉素、美罗培南三水合物和多尼培南水合物)引起的体内胆汁酸变化的作用机制。用这些抗生素厌氧孵育的大鼠粪便 16S rRNA 分析表明,妥布霉素特别诱导了肠道微生物群的变化。此外,妥布霉素被证明抑制了牛磺胆酸(TCA)的微生物去结合以及 TCA 在体外 Caco-2 细胞层上的转运,该细胞层用作模拟肠道胆汁酸重吸收的模型。抗生素在体外模型系统中引起的作用提供了新的和补充的见解,解释了抗生素对微生物群和粪便胆汁酸水平的影响,这些影响来自大鼠体内 28 天治疗。特别是,我们的结果提供了关于妥布霉素暴露时粪便中 TCA 水平升高的作用机制的见解。总之,本研究的结果提供了一个原理证明,即体外模型如何可用于阐明对胆汁酸稳态的体内影响,并深入了解抗生素(在这种情况下是妥布霉素)通过对肠道胆汁酸代谢和重吸收的影响对胆汁酸稳态的作用机制。