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Gut Microbiota-Based Pharmacokinetics and the Antidepressant Mechanism of Paeoniflorin

机译:基于肠道菌群的药代动力学和Pa药苷的抗抑郁机制

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Paeoniflorin, the main component of Xiaoyao Wan, presents low oral bioavailability and unclear antidepressant mechanism. To elucidate the potential reasons for the low bioavailability of paeoniflorin and explore its antidepressant mechanism from the perspective of the gut microbiota, here, a chronic unpredictable depression model and forced swimming test were firstly performed to examine the antidepressant effects of paeoniflorin. Then the pharmacokinetic study of paeoniflorin in rats was performed based on the gut microbiota; meanwhile, the gut microbiota incubated with paeoniflorin in vitro was used to identify the possible metabolites of paeoniflorin. Molecular virtual docking experiments together with the specific inhibitor tests were applied to investigate the mechanism of paeoniflorin metabolism by the gut microbiota. Finally, the intestinal microbiota composition was analyzed by 16S rRNA gene sequencing technology. The pharmacodynamics tests showed that paeoniflorin had significant antidepressant activity, but its oral bioavailability was 2.32%. Interestingly, we found paeoniflorin was converted into benzoic acid by the gut microbiota, and was mainly excreted through the urine with the gut metabolite benzoic acid as the prominent excreted form. Moreover, paeoniflorin could also regulate the composition of the gut microbiota by increasing the abundance of probiotics. Therefore, the metabolism effect of gut microbiota may be one of the main reasons for the low oral bioavailability of paeoniflorin. Additionally, paeoniflorin can be metabolized into benzoic acid via gut microbiota enzymes, which might exert antidepressant effects through the blood–brain barrier into the brain.
机译:逍遥丸的主要成分药苷口服生物利用度低,抗抑郁机制不清楚。为了阐明pa药苷生物利用度低的潜在原因,并从肠道菌群的角度探讨其抗抑郁作用的机理,本文首先进行了慢性不可预测的抑郁模型和强迫游泳试验,以研究pa药苷的抗抑郁作用。然后根据肠道菌群进行pa药苷在大鼠体内的药代动力学研究。同时,用pa药苷体外培养的肠道菌群鉴定了pa药苷可能的代谢产物。分子虚拟对接实验以及特异性抑制剂试验被用于研究肠道菌群对pa药苷代谢的机理。最后,通过16S rRNA基因测序技术分析了肠道菌群组成。药效学试验表明pa药苷具有明显的抗抑郁活性,但口服生物利用度为2.32%。有趣的是,我们发现pa药苷被肠道菌群转化为苯甲酸,并主要通过肠道代谢产物苯甲酸作为主要的排泄形式通过尿液排泄。此外,pa药苷还可以通过增加益生菌的含量来调节肠道菌群的组成。因此,肠道菌群的代谢作用可能是pa药苷口服生物利用度低的主要原因之一。此外,pa药苷可以通过肠道菌群酶代谢为苯甲酸,可能通过血脑屏障进入大脑而发挥抗抑郁作用。

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