Dept. of Psychiatry, LWL University Hospital, Ruhr University, Bochum, Germany.
Dept. of Psychiatry, LWL University Hospital, Ruhr University, Bochum, Germany.
Prog Neuropsychopharmacol Biol Psychiatry. 2021 Aug 30;110:110306. doi: 10.1016/j.pnpbp.2021.110306. Epub 2021 Mar 18.
Background Immunopathological concepts have been intensively discussed for schizophrenia. The polyriboinosinic-polyribocytidylic (PolyI:C) mouse model has been well validated to invasively study this disease. The intestinal microbiome exhibits broad immunological and neuronal activities. The relevance of microbiome alterations in the PolyI:C model to human schizophrenia should be explored. Methods Feces of offspring from mice mothers, who were administered to PolyI:C or NaCl (controls) at ED 9, were collected at PND 30 and 180 (PolyI:C and control mice (N = 32 each; half males and females). This was analyzed for bacterial 16S ribosomal DNA (rDNA) using a gut microbiome polymerase chain reaction (PCR) microarray tool. Results Differences were found in species richness of microbiome between animals of different ages (PND 30 and 180), but also between offspring from PolyI:C vs. NaCl treated mothers. In female mice at PND 30, the abundance of Prevotellaceae and Porphyromonadaceae was lower and that of Lactobacillales was higher, whereas in male mice at the same time point the abundance of four families of the Firmicutes phylum (Clostridia vadinBB60 group, Clostridiales Family XIII, Ruminococcaceae and Erysipelotrichaceae) was increased relative to the control group. Limitations No further analyses of cell types or cytokines involved in autoimmune gut and brain processes. Conclusions These finding seem to be similar to microbiome disturbances in patients with schizophrenia. The differential bacterial findings at day 30 (i.e., similar to the prodromal phase in patients with schizophrenia) correspond to the tremendous activation of the immune system with a strong increase in microglial cells which might be responsible for neuroplasticity reduction in cortical areas in patients with schizophrenia.
免疫病理学概念在精神分裂症中得到了深入探讨。聚肌胞苷酸(PolyI:C)小鼠模型已被充分验证,可用于深入研究该疾病。肠道微生物组具有广泛的免疫和神经活性。应该探索微生物组改变在 PolyI:C 模型中与人类精神分裂症的相关性。
在 ED 9 时给母鼠注射 PolyI:C 或 NaCl(对照),收集后代的粪便,在 PND 30 和 180 时进行分析(PolyI:C 和对照小鼠(N=32 只,雌雄各半)。使用肠道微生物组聚合酶链反应(PCR)微阵列工具分析细菌 16S 核糖体 DNA(rDNA)。
不同年龄(PND 30 和 180)动物之间以及 PolyI:C 与 NaCl 处理的母鼠的后代之间的微生物组物种丰富度存在差异。在 PND 30 的雌性小鼠中,Prevotellaceae 和 Porphyromonadaceae 的丰度较低,而 Lactobacillales 的丰度较高,而在同一时间点的雄性小鼠中,厚壁菌门(Clostridia vadinBB60 组、Clostridiales Family XIII、Ruminococcaceae 和 Erysipelotrichaceae)的四个家族的丰度增加与对照组相比。
未进一步分析自身免疫性肠道和大脑过程中涉及的细胞类型或细胞因子。
这些发现似乎与精神分裂症患者的微生物组紊乱相似。第 30 天的差异细菌发现(即类似于精神分裂症患者的前驱期)与免疫系统的巨大激活相对应,强烈增加小胶质细胞,这可能是精神分裂症患者皮质区神经可塑性降低的原因。