Journal Article

Injection of amyloid-β to lateral ventricle induces gut microbiota dysbiosis in association with inhibition of cholinergic anti-inflammatory pathways in Alzheimer’s disease

Liu, Xiao-li, Qian, Xiao-hang, Tang, Hui-dong, Chen, Guang, Chen, Sheng-di

2022

Overview

Background Alzheimer's disease (AD) is the most common neurodegenerative disease and its pathogenesis is still unclear. There is dysbiosis of gut microbiota in AD patients. More importantly, dysbiosis of the gut microbiota has been observed not only in AD patients, but also in patients with mild cognitive impairment (MCI). However, the mechanism of gut microbiota dysbiosis in AD is poorly understood. Cholinergic anti-inflammatory pathway is an important pathway for the central nervous system (CNS) regulation of peripheral immune homeostasis, especially in the gut. Therefore, we speculated that dysfunction of cholinergic anti-inflammatory pathway is a potential pathway for dysbiosis of the gut microbiota in AD. Methods In this study, we constructed AD model mice by injecting Aβ 1–42 into the lateral ventricle, and detected the cognitive level of mice by the Morris water maze test. In addition, 16S rDNA high-throughput analysis was used to detect the gut microbiota abundance of each group at baseline, 2 weeks and 4 weeks after surgery. Furthermore, immunofluorescence and western blot were used to detect alteration of intestinal structure of mice, cholinergic anti-inflammatory pathway, and APP process of brain and colon in each group. Results Aβ 1–42 i.c.v induced cognitive impairment and neuron damage in the brain of  mice. At the same time, Aβ 1–42 i.c.v induced alteration of gut microbiota at 4 weeks after surgery, while there was no difference at the baseline and 2 weeks after surgery. In addition, changes in colon structure and increased levels of pro-inflammatory factors were detected in Aβ 1–42 treatment group, accompanied by inhibition of cholinergic anti-inflammatory pathways. Amyloidogenic pathways in both the brain and colon were accelerated in Aβ 1–42 treatment group. Conclusions The present findings suggested that Aβ in the CNS can induce gut microbiota dysbiosis, alter intestinal structure and accelerate the amyloidogenic pathways, which were related to inhibiting cholinergic anti-inflammatory pathways.

• Publisher: BioMed Central,Springer Nature B.V,BMC
• Subject: Alzheimer's disease / Amyloidogenesis / Animal cognition / Animal models / Biomedical and Life Sciences / Biomedicine / Brain injury / Central nervous system / Cholinergic anti-inflammatory pathway / Cognitive ability / Colon / Digestive system / Dysbacteriosis / Feces / Gastrointestinal tract / Gut microbiota / Homeostasis / Immunofluorescence / Immunology / Inflammation / Intestinal microflora / Intestine / Microbiota / Nervous system / Neurobiology / Neurodegenerative diseases / Neurology / Neurosciences / Pathology / Patients / Permeability / Rodents / rRNA 16S / Surgery / The microbiota–gut–brain axis / Ventricle / Ventricles (cerebral) / β-Amyloid