Yu Jin-Bo, Zhao Zhen-Xiong, Peng Ran, Pan Li-Bin, Fu Jie, Ma Shu-Rong, Han Pei, Cong Lin, Zhang Zheng-Wei, Sun Li-Xin, Jiang Jian-Dong, Wang Yan
Department of Traditional Chinese Medicine, School of Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, China.
State Key Laboratory of Bioactive Substance and Function of Natural Medicines Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Front Pharmacol. 2019 Mar 20;10:268. doi: 10.3389/fphar.2019.00268. eCollection 2019.
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 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.
芍药苷是逍遥丸的主要成分,其口服生物利用度低,抗抑郁机制尚不明确。为阐明芍药苷生物利用度低的潜在原因,并从肠道微生物群的角度探索其抗抑郁机制,本研究首先进行了慢性不可预测性抑郁模型和强迫游泳试验,以检验芍药苷的抗抑郁作用。然后基于肠道微生物群进行了芍药苷在大鼠体内的药代动力学研究;同时,用与芍药苷共孵育的肠道微生物群来鉴定芍药苷可能的代谢产物。应用分子虚拟对接实验和特异性抑制剂试验来研究肠道微生物群对芍药苷的代谢机制。最后,采用16S rRNA基因测序技术分析肠道微生物群的组成。药效学试验表明,芍药苷具有显著的抗抑郁活性,但其口服生物利用度为2.32%。有趣的是,我们发现芍药苷被肠道微生物群转化为苯甲酸,并主要以肠道代谢产物苯甲酸为主要排泄形式通过尿液排出。此外,芍药苷还可通过增加益生菌的丰度来调节肠道微生物群的组成。因此,肠道微生物群的代谢作用可能是芍药苷口服生物利用度低的主要原因之一。此外,芍药苷可通过肠道微生物群酶代谢为苯甲酸,苯甲酸可能通过血脑屏障进入大脑发挥抗抑郁作用。