State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Research Units of Infectious Disease and Microecology, Chinese Academy of Medical Sciences, Hangzhou 310003, China.
Nutrients. 2021 Mar 15;13(3):940. doi: 10.3390/nu13030940.
Anxiety is one of the complications of metabolic disorders (MDs). Obeticholic acid (OCA), the bile acids (BAs) derivative, is a promising agent for improving MDs in association with gut dysbiosis. Yet, its protective effect on MDs-driven anxiety remains unknown. Here, we assessed the serum biochemical parameters and behavioral performance by open field and Morris water maze tests in HFHS diet-induced MDs mice after OCA intervention for nine and 18 weeks. Moreover, antibiotics intervention for microbial depletion was conducted simultaneously. We found that OCA treatment inhibited the initiation and progression of anxiety in HFHS diet-MDs mice via a microbiota-BAs-brain axis: OCA decreased the neuroinflammatory microglia and IL-1β expression in the hippocampus, reversed intestinal barrier dysfunction and serum proinflammatory LPS to a normal level, modified the microbial community, including the known anxiety-related Rikenellaceae and , and improved the microbial metabolites especially the increased BAs in feces and circulation. Moreover, the OCA-reversed bile acid taurocholate linked disordered serum lipid metabolites and indole derivatives to anxiety as assessed by network analysis. Additionally, microbial depletion with antibiotics also improved the anxiety, microgliosis and BAs enrichment in the experimental MDs mice. Together, these findings provide microbiota-BAs-brain axis as a novel therapeutic target for MDs-associated neuropsychiatric disorders.
焦虑是代谢紊乱(MDs)的并发症之一。奥贝胆酸(OCA)是一种胆汁酸(BAs)衍生物,有望改善与肠道菌群失调相关的 MDs。然而,其对 MDs 相关焦虑的保护作用尚不清楚。在这里,我们在 HFHS 饮食诱导的 MDs 小鼠中,通过开放场和 Morris 水迷宫试验评估了 OCA 干预 9 周和 18 周后的血清生化参数和行为表现。此外,同时进行了抗生素干预以消耗微生物。我们发现,OCA 通过微生物群-BAs-脑轴抑制 HFHS 饮食-MDs 小鼠焦虑的发生和进展:OCA 降低了海马体中神经炎症小胶质细胞和 IL-1β 的表达,将肠道屏障功能障碍和血清促炎 LPS 恢复到正常水平,改变了微生物群落,包括已知与焦虑相关的 Rikenellaceae 和 ,并改善了微生物代谢物,特别是粪便和循环中的 BAs 增加。此外,网络分析表明,OCA 逆转的胆酸牛磺胆酸盐与焦虑相关的血清脂质代谢物和吲哚衍生物紊乱有关。此外,用抗生素进行微生物消耗也改善了实验性 MDs 小鼠的焦虑、小胶质细胞增生和 BAs 富集。总之,这些发现为 MDs 相关神经精神疾病提供了微生物群-BAs-脑轴作为一种新的治疗靶点。