Kaur Harpreet, Golovko Svetlana, Golovko Mikhail Y, Singh Surjeet, Darland Diane C, Combs Colin K
Department of Biomedical Sciences, University of North Dakota, School of Medicine and Health Sciences, Grand Forks, ND, USA.
Department of Neuroscience, Canadian Centre for Behavioural Neuroscience (CCBN), University of Lethbridge, Lethbridge, AB, Canada.
J Alzheimers Dis. 2020;76(3):1083-1102. doi: 10.3233/JAD-200436.
The intestinal microbiota and its metabolites, particularly short-chain fatty acids (SCFAs), have been implicated in immune function, host metabolism, and even behavior.
This study was performed to investigate whether probiotic administration influences levels of intestinal microbiota and their metabolites in a fashion that may attenuate brain changes in a mouse model of Alzheimer's disease (AD).
C57BL/6 wild-type (WT) mice were compared to AppNL-G-Fmice. The animals were treated with either vehicle or probiotic (VSL#3) for 8 weeks. Fecal microbiome analysis along with Aβ, GFAP, Iba-1, c-Fos, and Ki-67 immunohistochemistry was done. SCFAs were analyzed in serum and brains using UPLC-MS/MS.
Probiotic (VSL#3) supplementation for 2 months resulted in altered microbiota in both WT and AppNL-G-Fmice. An increase in serum SCFAs acetate, butyrate, and lactate were found in both genotypes following VSL#3 treatment. Propionate and isobutyrate were only increased in AppNL-G-Fmice. Surprisingly, VSL#3 only increased lactate and acetate in brains of AppNL-G-Fmice. No significant differences were observed between vehicle and VSL#3 fed AppNL-G-Fhippocampal immunoreactivities of Aβ, GFAP, Iba-1, and Ki-67. However, hippocampal c-Fos staining increased in VSL#3 fed AppNL-G-Fmice.
These data demonstrate intestinal dysbiosis in the AppNL-G-Fmouse model of AD. Probiotic VSL#3 feeding altered both serum and brain levels of lactate and acetate in AppNL-G-Fmice correlating with increased expression of the neuronal activity marker, c-Fos.
肠道微生物群及其代谢产物,特别是短链脂肪酸(SCFAs),与免疫功能、宿主代谢甚至行为有关。
本研究旨在探讨给予益生菌是否会以一种可能减轻阿尔茨海默病(AD)小鼠模型脑变化的方式影响肠道微生物群及其代谢产物的水平。
将C57BL/6野生型(WT)小鼠与AppNL-G-F小鼠进行比较。动物接受载体或益生菌(VSL#3)治疗8周。进行粪便微生物组分析以及Aβ、GFAP、Iba-1、c-Fos和Ki-67免疫组织化学检测。使用超高效液相色谱-串联质谱法(UPLC-MS/MS)分析血清和脑中的短链脂肪酸。
补充益生菌(VSL#3)2个月导致WT和AppNL-G-F小鼠的微生物群发生改变。VSL#3治疗后,两种基因型的血清乙酸盐、丁酸盐和乳酸盐短链脂肪酸均增加。丙酸盐和异丁酸盐仅在AppNL-G-F小鼠中增加。令人惊讶的是,VSL#3仅增加了AppNL-G-F小鼠脑中的乳酸盐和乙酸盐。在给予载体和VSL#3的AppNL-G-F小鼠的海马中,Aβ、GFAP、Iba-1和Ki-67的免疫反应性未观察到显著差异。然而,给予VSL#3的AppNL-G-F小鼠海马中的c-Fos染色增加。
这些数据证明了AD的AppNL-G-F小鼠模型中存在肠道菌群失调。给予益生菌VSL#3改变了AppNL-G-F小鼠血清和脑中乳酸盐和乙酸盐的水平,这与神经元活动标志物c-Fos的表达增加相关。