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Lactobacillus plantarum PS128 prevents cognitive dysfunction in Alzheimer's disease mice by modulating propionic acid levels, glycogen synthase kinase 3 beta activity, and gliosis.

Authors :
Huang, Hei-Jen
Chen, Jie-Ling
Liao, Jian-Fu
Chen, Yu-Hsin
Chieu, Min-Wei
Ke, Ya-Yun
Hsu, Chih-Chieh
Tsai, Ying-Chieh
Hsieh-Li, Hsiu Mei
Source :
BMC Complementary Medicine & Therapies; 10/9/2021, Vol. 21 Issue 1, p1-16, 16p, 2 Color Photographs, 2 Black and White Photographs, 1 Illustration, 1 Diagram, 2 Charts, 1 Graph
Publication Year :
2021

Abstract

Background: According to recent evidence, psychobiotics exert beneficial effects on central nervous system-related diseases, such as mental disorders. Lactobacillus plantarum PS128 (PS128), a novel psychobiotic strain, improves motor function, depression, and anxiety behaviors. However, the psychobiotic effects and mechanisms of PS128 in Alzheimer's disease (AD) remain to be explored. Objectives: The goal of the current study was to evaluate the beneficial effects of PS128 and to further elucidate its mechanism in AD mice. Methods: PS128 (10<superscript>10</superscript> colony-forming unit (CFU)/ml) was administered via oral gavage (o.g.) to 6-month-old male wild-type B6 and 3 × Tg-AD mice (harboring the PS1M146V, APPswe and TauP30IL transgenes) that received an intracerebroventricular injection of streptozotocin (icv-STZ, 3 mg/kg) or vehicle (saline) for 33 days. After serial behavioral tests, fecal short-chain fatty acid levels and AD-related pathology were assessed in these mice. Results: Our findings show that intracerebroventricular injection of streptozotocin accelerated cognitive dysfunction associated with increasing levels of glycogen synthase kinase 3 beta (GSK3β) activity, tau protein phosphorylation at the T231 site (pT231), amyloid-β (Aβ) deposition, amyloid-β protein precursor (AβPP), β-site AβPP-cleaving enzyme (BACE1), gliosis, fecal propionic acid (PPA) levels and cognition-related neuronal loss and decreasing postsynaptic density protein 95 (PSD95) levels in 3 × Tg-AD mice. PS128 supplementation effectively prevented the damage induced by intracerebroventricular injection of streptozotocin in 3 × Tg-AD mice. Conclusions: Based on the experimental results, intracerebroventricular injection of streptozotocin accelerates the progression of AD in the 3 × Tg-AD mice, primarily by increasing the levels of gliosis, which were mediated by the propionic acid and glycogen synthase kinase 3 beta pathways. PS128 supplementation prevents damage induced by intracerebroventricular injection of streptozotocin by regulating the propionic acid levels, glycogen synthase kinase 3 beta activity, and gliosis in 3 × Tg-AD mice. Therefore, we suggest that PS128 supplementation is a potential strategy to prevent and/or delay the progression of AD. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
26627671
Volume :
21
Issue :
1
Database :
Complementary Index
Journal :
BMC Complementary Medicine & Therapies
Publication Type :
Academic Journal
Accession number :
152928225
Full Text :
https://doi.org/10.1186/s12906-021-03426-8