Chiral nanoparticle-remodeled gut microbiota alleviates neurodegeneration via the gut–brain axis

IF 17 Q1 CELL BIOLOGY Nature aging Pub Date : 2023-11-09 DOI:10.1038/s43587-023-00516-9
Xiao Guo, Chen Li, Jia Zhang, Maozhong Sun, Jun Xu, Chuanlai Xu, Hua Kuang, Liguang Xu
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Abstract

Alzheimer’s disease (AD) is characterized by amyloid-β accumulation in the brain and hyperphosphorylated tau aggregation, as well as neuroinflammation. The gut–brain axis has emerged as a therapeutic target in neurodegenerative diseases by modulating metabolic activity, neuroimmune functions and sensory neuronal signaling. Here we investigate interactions between orally ingested chiral Au nanoparticles and the gut microbiota in AD mice. Oral administration of chiral Au nanoparticles restored cognitive abilities and ameliorated amyloid-β and hyperphosphorylated tau pathologies in AD mice via alterations in the gut microbiome composition and an increase in the gut metabolite, indole-3-acetic acid, which was lower in serum and cerebrospinal fluid of patients with AD compared with age-matched controls. Oral administration of indole-3-acetic acid was able to penetrate the blood–brain barrier and alleviated cognitive decline and pathology including neuroinflammation in AD mice. These findings provide a promising therapeutic target for the amelioration of neuroinflammation and treatment of neurodegenerative diseases. Guo et al. demonstrate that oral administration of chiral nanoparticles ameliorates Alzheimer’s disease-associated pathology and cognitive decline in mice via an increase in the gut metabolite, indole-3-acetic acid, potentially a therapeutic target.

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手性纳米颗粒重塑的肠道微生物群通过肠脑轴缓解神经退行性变。
阿尔茨海默病(AD)的特征是淀粉样蛋白-β在大脑中积聚、tau过度磷酸化聚集以及神经炎症。肠脑轴通过调节代谢活动、神经免疫功能和感觉神经元信号,已成为神经退行性疾病的治疗靶点。在这里,我们研究了口服手性Au纳米颗粒与AD小鼠肠道微生物群之间的相互作用。口服手性Au纳米颗粒通过改变肠道微生物组组成和增加肠道代谢产物吲哚-3-乙酸,恢复了AD小鼠的认知能力,改善了淀粉样蛋白-β和过度磷酸化的tau病理,与年龄匹配的对照组相比,AD患者的血清和脑脊液中吲哚-3-乙酸含量较低。口服吲哚-3-乙酸能够穿透血脑屏障,缓解AD小鼠的认知能力下降和病理学,包括神经炎症。这些发现为改善神经炎症和治疗神经退行性疾病提供了一个有前景的治疗靶点。
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