Xuefu Zhuyu Capsule alleviates depression in post-stroke depression model rats via modulation of the gut microbiota-gut-brain axis.

Drug discoveries & therapeutics Pub Date : 2026-03-04 Epub Date: 2026-02-13 DOI:10.5582/ddt.2025.01120
Bowen Jin, Yuqian Wang, Zhaowei Zhang, Xuejin Fan, Yanjun Zhang, Pengwei Zhuang
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Abstract

Xuefu Zhuyu Capsule (XFZY) demonstrated potential in alleviating post-stroke depression (PSD), a condition whose underlying mechanisms may involve the gut-brain axis. This study aimed to explore the therapeutic effects of XFZY on PSD and its possible modulation of the gut microbiota-gut-brain axis in a rat model. Wistar rats were randomly assigned to sham, PSD, three XFZY dose (0.216, 0.432, 0.864 g/kg), and fluoxetine (1.80 mg/kg) groups (n = 12 per group). The PSD model was established using transient middle cerebral artery occlusion (t-MCAO) combined with chronic unpredictable mild stress (CUMS), followed by 28 days of XFZY administration. In a separate experiment, gut microbiota was depleted via antibiotic cocktails, with rats divided into sham, PSD, XFZY medium Dose (XFM), pseudo-germ-free (PGF) and PGF + XFM (PGFX) groups. Behavioral tests indicated that XFZY ameliorated depressive-like behaviors, with the medium dose (0.432 g/kg) showing the most significant effect. Histological analysis using hematoxylin and eosin (H&E) and Nissl staining revealed that XFZY alleviated colonic and neuronal damage. Furthermore, 16S rRNA sequencing and gas chromatography revealed that XFZY modulated gut microbiota composition, increased species richness, and elevated levels of short-chain fatty acids such as acetic acid, propionic acid, and butyric acid. Enzyme-Linked Immunosorbent Assay (ELISA) results showed that XFZY reduced pro-inflammatory cytokines - interleukin-1β (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α), while immunohistochemistry indicated enhanced intestinal barrier function and reduced neuroinflammation. Furthermore, after depletion of gut microbiota using antibiotic cocktails, these therapeutic effects of XFZY were abolished. In summary, XFZY may alleviate PSD by modulating the gut microbiota and regulating the gut-brain axis, offering a promising direction for future therapeutic research.

血府助瘀胶囊通过调节肠道菌群-肠-脑轴减轻脑卒中后抑郁模型大鼠的抑郁。
脑卒中后抑郁(PSD)的潜在机制可能与肠脑轴有关。本研究旨在探讨XFZY对PSD大鼠模型的治疗作用及其对肠道微生物-肠-脑轴的可能调节作用。Wistar大鼠随机分为假手术组、PSD组、XFZY 3个剂量组(0.216、0.432、0.864 g/kg)和氟西汀(1.80 mg/kg)组(每组12只)。采用短暂性大脑中动脉闭塞(t-MCAO)联合慢性不可预测轻度应激(CUMS)建立PSD模型,并给予XFZY 28 d。在另一个实验中,通过抗生素鸡尾酒消耗肠道微生物群,将大鼠分为假药组、PSD组、XFZY中剂量组(XFM)、伪无菌组(PGF)和PGF + XFM组(PGFX)。行为学测试显示,XFZY能改善抑郁样行为,其中中剂量(0.432 g/kg)效果最显著。苏木精和伊红(H&E)和尼氏染色的组织学分析显示,XFZY减轻了结肠和神经元的损伤。此外,16S rRNA测序和气相色谱分析显示,XFZY可调节肠道菌群组成,增加物种丰富度,并提高短链脂肪酸(如乙酸、丙酸和丁酸)的水平。酶联免疫吸附试验(ELISA)结果显示,XFZY可降低促炎细胞因子-白细胞介素-1β (IL-1β)、白细胞介素-6 (IL-6)和肿瘤坏死因子-α (TNF-α),免疫组化显示肠道屏障功能增强,神经炎症减轻。此外,在使用抗生素鸡尾酒耗尽肠道微生物群后,XFZY的这些治疗作用被消除。综上所述,XFZY可能通过调节肠道菌群和调节肠脑轴来缓解PSD,为未来的治疗研究提供了一个有希望的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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Agilent 6890N gas chromatograph
2
DB-FFAP column
3
ABI GeneAmp 9902 thermal cycler
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HRP-conjugated secondary antibody
5
anti-MUC2
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anti-Occludin
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anti-ZO-1
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IL-1β ELISA kit
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IL-6 ELISA kit
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TNF-α ELISA kit
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Illumina NovaSeq 6000
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EthoVision XT
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anti-Iba1
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OMEGA DNA columns
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fluoxetine
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TGuide S96 Magnetic Soil/Stool DNA Kit
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Xuefu Zhuyu capsule
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Wistar rats
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AB chromogen
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Alcian blue–Periodic acid–Schiff staining kit
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goat serum
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Hematoxylin and eosin staining kit
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paraformaldehyde
30525-89-4
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28
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sodium citrate buffer
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