修改后的Xiaoyaosan通过重塑肠道微生物群和氨酸代谢来拯救类似抑郁症的行为
Yunhao Zhao1, Qi Wang1, Zhenning Wu1
1Modern Research Center for Traditional Chinese Medicine, Shanxi University, 030006 Taiyuan, Shanxi, China.
Phytomedicine : international journal of phytotherapy and phytopharmacology
|September 13, 2025
概括
修改后的小山 (MXYS) 通过改变肠道微生物来减少白来缓解抑郁症中的社会回避. 恢复白水平可以改善抑郁行为和海马氧化应激.
科学领域:
- 神经科学是一个神经科学.
- 微生物学 微生物学
- 代谢学 代谢学 代谢学
背景情况:
- 社会回避是抑郁症的一个关键症状.
- 修改的Xiaoyaosan (MXYS) 在治疗社会回避的机制是不清楚的.
研究的目的:
- 调查MXYS如何缓解社会回避.
- 专注于肠道微生物群和白代谢的作用.
主要方法:
- 使用慢性社会失败压力 (CSDS) 鼠标模型.
- 使用16S rRNA测序和LC-MS.分析了肠道微生物群和代谢物.
- 进行了便微生物群移植 (FMT) 和有针对性的代谢分析.
主要成果:
- 在CSDS小鼠中,MXYS减少了社交回避和类似抑郁症的行为.
- 确定了白代谢作为治疗标,由MXYS调节.
- 显示肠道微生物群调解MXYS效应;氨酸补充剂逆转了抑郁行为.
结论:
- MXYS通过肠道微生物群介导的氨酸降解来缓解社会回避.
- 恢复了全身白水平,改善了海马体的氧化应激.
关键词:
慢性社会失败压力模型我们的肠道微生物群.叶氨酸 (Leucine) 是一种蛋白质.微生物生物衍生的代谢物.修改后的Xiaoyaosanosan是一种修改后的Xiaoyaosan社会回避行为是社会回避行为.更多相关视频
08:15Network Pharmacology and Validation of the Antidepressant Mechanisms of Qiangzhifang in a Chronic Restraint Stress-induced Depression Rat Model
Published on: June 6, 2025
527
07:49Intracerebroventricular Delivery of Gut-Derived Microbial Metabolites in Freely Moving Mice
Published on: June 2, 2022
3.7K
相关概念视频
Antidepressant Drugs: MAOIs and Other Agents
828
Atypical antidepressants, including bupropion (Wellbutrin), mirtazapine (Remeron), nefazodone (Serzone), trazodone (Desyrel), and vilazodone (Viibryd), offer unique mechanisms of action. Bupropion weakly inhibits dopamine and norepinephrine reuptake, aiding depression treatment and smoking cessation, with a low risk of sexual dysfunction. Mirtazapine enhances serotonin and norepinephrine neurotransmission, leading to sedation, increased appetite, and weight gain. As a result, it helps treat...
828
Long-term Depression
33.1K
Long-term depression, or LTD, is one of the ways by which synaptic plasticity—changes in the strength of chemical synapses—can occur in the brain. LTD is the process of synaptic weakening that occurs over time between pre and postsynaptic neuronal connections. The synaptic weakening of LTD works in opposition to synaptic strengthening by long-term potentiation (LTP) and together are the main mechanisms that underlie learning and memory.
33.1K
