体外循环致术后谵妄人源肠道菌群模型大鼠的构建及评价

Establishment and evaluation on a rat model of postoperative delirium induced by cardiopulmonary bypass with human gut microbiota

  • 摘要:
    目的 采用粪菌移植技术构建体外循环致术后谵妄(POD)人源肠道菌群模型大鼠,并基于生物信息学、细胞因子分析、行为学等方法对模型进行评价。
    方法 选取SPF级成年雄性SD大鼠,体质量400~450 g。对大鼠进行1周的Morris水迷宫训练,剔除差异后构建伪无菌大鼠模型,成功后将20只模型大鼠随机分为接种健康人源粪菌滤液组(CON组)和接种POD患者粪菌滤液组(POD组)。2周后造模完成后开展行为学测试,收集大鼠粪便进行宏基因组学测序。采用脊椎脱臼法处死大鼠,取血液及脑组织样本进行细胞因子、组织病理学检查。
    结果 与CON组相比,POD组阿克曼菌科、普雷沃菌科和嗜黏蛋白-艾克曼菌的相对丰度显著增高,乳酸杆菌科和地中海-玛斯里菌的相对丰度降低,差异均有统计学意义(P < 0.05)。POD组大鼠血清白细胞介素(IL)-1β、IL-6和肿瘤坏死因子(TNF)-α水平均高于CON组大鼠,差异有统计学意义(P < 0.05)。POD组苏木精-伊红染色可见核固缩、核浓染的神经元。造模后, POD组Morris水迷宫平均潜伏期长于CON组,差异有统计学意义(P < 0.05)。
    结论 本研究采用粪菌移植技术获得体外循环致POD人源肠道菌群模型大鼠,其肠道菌群结构丰度、与POD相关的炎症因子水平、Morris水迷宫测试等指标变化与体外循环致POD患者的临床表现相似。

     

    Abstract:
    Objective To establish a rat model of postoperative delirium (POD) induced by cardiopulmonary bypass with human gut microbiota using fecal microbiota transplantation (FMT) technology, and evaluate the model based on bioinformatics, cytokine analysis, and behavioral testing methods.
    Methods SPF-grade adult male SD rats weighing 400 to 450 g were selected. After undergoing a week of Morris water maze training, rats with consistent performance were used to construct pseudo-germ-free rat models. Subsequently, 20 successfully modeled rats were randomly divided into two groups: (CON group receiving fecal microbiota filtrate from healthy individuals) and (POD group receiving fecal microbiota filtrate from POD patients). Behavioral tests were conducted two weeks after modeling, and rat feces were collected for metagenomic sequencing. Rats were euthanized by cervical dislocation, and blood and brain tissue samples were collected for cytokine and histopathological examinations.
    Results Compared with the CON group, the POD group exhibited significantly increased relative abundances of Akkermansiaceae, Prevotellaceae, and Akkermansia muciniphila, while the relative abundances of Lactobacillaceae and Mediterraneibacter massiliensis decreased significantly (P < 0.05). Serum levels of interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α were significantly higher in the POD group than those in the CON group (P < 0.05). Hematoxylin-eosin (HE) staining in the POD group revealed neurons with pyknotic and hyperchromatic nuclei. After modeling, the average latency in the Morris water maze was significantly longer in the POD group than that in the CON group (P < 0.05).
    Conclusion This study utilizes fecal microbiota transplantation technology to establish a rat model of POD induced by cardiopulmonary bypass with human gut microbiota. The changes in gut microbiota structure abundance, levels of POD-related inflammatory factors, and Morris water maze test results in this model are similar to the clinical manifestations observed in patients with POD induced by cardiopulmonary bypass.

     

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