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Neuroprotective effects of fecal microbiota transplantation on MPTP-induced Parkinson's disease mice: Gut microbiota, glial reaction and TLRLI/TNF-alpha signaling pathway

机译:FeCal Microbiota移植对MPTP诱导的帕金森病小鼠的神经保护作用:肠道微生物,胶质反应和TLRLI / TNF-α信号通路

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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 TLRII/TNF-alpha 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-alpha signaling. (C) 2018 Elsevier Inc. All rights reserved.
机译:帕金森病(PD)患者展示肠道微生物群组合物的改变。然而,肠道微生物脱泻和PD的发病机制之间的机制仍然是未探测的,并且没有公认的疗法可停止或缓慢PD进展。在这里,我们发现从PD小鼠诱导PD小鼠的肠道微生物群诱导的电动机损伤和正常小鼠的纹状体神经递质减少。 16S rRNA的测序显示,PLUM型和序列梭菌的术术和序列术术中的PD小鼠的粪便样本中粪便样本增加,随着粪便短链脂肪酸(SCFA)的增加。值得注意的是,粪便微生物会移植(FMT)降低了肠道微生物脱泻,降低了粪便SCFA,缓解了物理损伤和增加了PD小鼠的5-HT含量。此外,FMT降低了体内NIGRA中的微胶质细胞和星形胶质细胞的激活,并降低了肠和脑中的TLRII / TNF-α信号通路组分的表达。我们的研究表明,肠道微生物脱泻病涉及PD发病机制,并且FMT可以通过抑制神经炎症和减少TLR4 / TNF-α信号来保护PD小鼠。 (c)2018年Elsevier Inc.保留所有权利。

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