Luo Yun-Mei, Dong Lan, Li Ye-Li, Lin Mu, Xie Dian-You, Gao Jian-Mei, Zhang Yuan-Dong, Zhu Yi Zhun, Gong Qi-Hai
School of Pharmacy, Faculty of Medicine, Macau University of Science and Technology, Macau, China.
Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi, China.
Phytother Res. 2025 Nov;39(11):5159-5173. doi: 10.1002/ptr.70103. Epub 2025 Sep 25.
Obesity can lead to depression via the microbiota-gut-brain axis. Icariside II (ICS II), a flavonoid compound derived from the traditional Chinese medicine Herbal Epimedium, exerts excellent neuroprotective effects. However, the pharmacological effects and underlying mechanisms of ICS II in obesity-induced depression remain unexplored. The present study aims to investigate whether ICS II can mitigate depression induced by a high-fat diet (HFD) in mice through modulating the microbiota-gut-brain axis. Metabolic parameters were reflected through changes in body weight and blood lipids, while depressive phenotypes were evaluated through behavioral tests and neurotransmitter analysis. The microbiota composition was analyzed by 16S ribosomal RNA gene sequencing, and short chain fatty acids (SCFAs) were detected by liquid chromatography-tandem mass spectrometry. The gut barrier and brain blood barrier (BBB) functions were observed by pathological methods. Fecal microbiota transplantation was used to demonstrate the causality of microbiota-mediated effects. The results showed that ICS II alleviated obesity status and depressive-like behaviors. ICS II reshaped gut microbiota and increased SCFAs. Meanwhile, ICS II relieved gut barrier impairment and systemic inflammation. In the brain, ICS II alleviated neuroinflammation and BBB injury. Intriguingly, fecal microbiota from ICS II-treated HFD mice improved depressive-like behaviors, intestinal barrier dysfunction, and BBB damage compared with those receiving microbiota from HFD mice. Our findings reveal for the first time that ICS II improves the obesity-related metabolic dysregulation and alleviates HFD-induced depression via the microbiota-gut-brain axis. Overall, this study indicates that ICS II is a potential candidate compound for treating obesity-related mental diseases.
肥胖可通过微生物群-肠道-脑轴导致抑郁。淫羊藿苷II(ICS II)是一种从传统中药淫羊藿中提取的黄酮类化合物,具有出色的神经保护作用。然而,ICS II在肥胖诱导的抑郁中的药理作用及潜在机制仍未得到探索。本研究旨在探讨ICS II是否能通过调节微生物群-肠道-脑轴减轻高脂饮食(HFD)诱导的小鼠抑郁。通过体重和血脂变化反映代谢参数,同时通过行为测试和神经递质分析评估抑郁表型。通过16S核糖体RNA基因测序分析微生物群组成,采用液相色谱-串联质谱法检测短链脂肪酸(SCFAs)。通过病理方法观察肠道屏障和脑血屏障(BBB)功能。采用粪便微生物群移植来证明微生物群介导作用的因果关系。结果显示,ICS II减轻了肥胖状态和抑郁样行为。ICS II重塑了肠道微生物群并增加了SCFAs。同时,ICS II缓解了肠道屏障损伤和全身炎症。在大脑中,ICS II减轻了神经炎症和BBB损伤。有趣的是,与接受HFD小鼠微生物群的小鼠相比,接受ICS II处理的HFD小鼠的粪便微生物群改善了抑郁样行为、肠道屏障功能障碍和BBB损伤。我们的研究结果首次揭示,ICS II通过微生物群-肠道-脑轴改善了肥胖相关的代谢失调并减轻了HFD诱导的抑郁。总体而言,本研究表明ICS II是治疗肥胖相关精神疾病的潜在候选化合物。