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微生物群调节可抵抗阿尔茨海默病的进展,影响神经元蛋白水解和肠道激素的血浆水平。

Microbiota modulation counteracts Alzheimer's disease progression influencing neuronal proteolysis and gut hormones plasma levels.

机构信息

School of Biosciences and Veterinary Medicine, University of Camerino, via Gentile III da Varano, 62032, Camerino, (MC), Italy.

Gastrointestinal Laboratory, Department of Small Animal Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Texas A&M University, College Station, USA.

出版信息

Sci Rep. 2017 May 25;7(1):2426. doi: 10.1038/s41598-017-02587-2.

Abstract

Gut microbiota has a proven role in regulating multiple neuro-chemical pathways through the highly interconnected gut-brain axis. Oral bacteriotherapy thus has potential in the treatment of central nervous system-related pathologies, such as Alzheimer's disease (AD). Current AD treatments aim to prevent onset, delay progression and ameliorate symptoms. In this work, 3xTg-AD mice in the early stage of AD were treated with SLAB51 probiotic formulation, thereby affecting the composition of gut microbiota and its metabolites. This influenced plasma concentration of inflammatory cytokines and key metabolic hormones considered therapeutic targets in neurodegeneration. Treated mice showed partial restoration of two impaired neuronal proteolytic pathways (the ubiquitin proteasome system and autophagy). Their cognitive decline was decreased compared with controls, due to a reduction in brain damage and reduced accumulation of amyloid beta aggregates. Collectively, our results clearly prove that modulation of the microbiota induces positive effects on neuronal pathways that are able to slow down the progression of Alzheimer's disease.

摘要

肠道微生物群在通过高度相互关联的肠脑轴调节多种神经化学途径方面发挥着已被证实的作用。口腔细菌疗法因此具有治疗中枢神经系统相关疾病(如阿尔茨海默病)的潜力。目前的阿尔茨海默病治疗方法旨在预防发病、延缓进展和改善症状。在这项工作中,处于阿尔茨海默病早期的 3xTg-AD 小鼠接受了 SLAB51 益生菌配方的治疗,从而影响了肠道微生物群及其代谢物的组成。这影响了被认为是神经退行性变治疗靶点的炎症细胞因子和关键代谢激素的血浆浓度。与对照组相比,接受治疗的小鼠表现出两种受损神经元蛋白水解途径(泛素蛋白酶体系统和自噬)的部分恢复。由于脑损伤减少和淀粉样β 聚集体积累减少,它们的认知能力下降减少。总之,我们的结果清楚地证明了微生物群的调节可以对神经元途径产生积极影响,从而减缓阿尔茨海默病的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/391a/5445077/7b4228fefd6c/41598_2017_2587_Fig2_HTML.jpg

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