粪便细菌疗法
神经保护
MPTP公司
肠道菌群
生物
TLR4型
帕金森病
肿瘤坏死因子α
肠-脑轴
移植
医学
炎症
内科学
免疫学
神经科学
微生物学
抗生素
疾病
艰难梭菌
作者
Meng‐Fei Sun,Ying‐Li Zhu,Zhi-Lan Zhou,Xue-Bing Jia,Yi‐Da Xu,Qin Yang,Chun Cui,Yan‐Qin Shen
标识
DOI:10.1016/j.bbi.2018.02.005
摘要
Parkinson's disease (PD) patients display alterations in gut microbiota composition. However, mechanism between gut microbial dysbiosis and pathogenesis of PD remains unexplored, and no recognized therapies are available to halt or slow progression of PD. Here we identified that gut microbiota from PD mice induced motor impairment and striatal neurotransmitter decrease on normal mice. Sequencing of 16S rRNA revealed that phylum Firmicutes and order Clostridiales decreased, while phylum Proteobacteria, order Turicibacterales and Enterobacteriales increased in fecal samples of PD mice, along with increased fecal short-chain fatty acids (SCFAs). Remarkably, fecal microbiota transplantation (FMT) reduced gut microbial dysbiosis, decreased fecal SCFAs, alleviated physical impairment, and increased striatal DA and 5-HT content of PD mice. Further, FMT reduced the activation of microglia and astrocytes in the substantia nigra, and reduced expression of TLR4/TNF-α signaling pathway components in gut and brain. Our study demonstrates that gut microbial dysbiosis is involved in PD pathogenesis, and FMT can protect PD mice by suppressing neuroinflammation and reducing TLR4/TNF-α signaling.
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