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Probiotic Bifidobacterium breve MCC1274 Mitigates Alzheimer's Disease-Related Pathologies in Wild-Type Mice
Mona Abdelhamid1, Chunyu Zhou1, Cha-Gyun Jung1
1Department of Biochemistry, Graduate School of Medical Sciences, Nagoya City University, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Aichi, Nagoya 467-8601, Japan.
Abstract:
Probiotics improve brain function, including memory and cognition, via the microbiome-gut-brain axis. Oral administration of Bifidobacterium breve MCC1274 (B. breve MCC1274) improves cognitive function in App mice and mild cognitive impairment (MCI) subjects, and mitigates Alzheimer's disease (AD)-like pathologies. However, its effects on wild-type (WT) mice have not yet been explored. Thus, the effects of B. breve MCC1274 on AD-like pathologies in two-month-old WT mice were investigated, which were orally administered B. breve MCC1274 for four months. Aβ levels, amyloid precursor protein (APP), APP processing enzymes, phosphorylated tau, synaptic protein levels, glial activity, and cell proliferation in the subgranular zone of the dentate gyrus were evaluated. Data analysis was performed using Student's t-test, and normality was tested using the Shapiro-Wilk test. Oral administration of B. breve MCC1274 in WT mice decreased soluble hippocampal Aβ42 levels by reducing presenilin1 protein levels, and reduced phosphorylated tau levels. It also activated the protein kinase B (Akt)/glycogen synthase kinase-3β (GSK-3β) pathway, which may be responsible for the reduction in presenilin1 levels and inhibition of tau phosphorylation. B. breve MCC1274 supplementation attenuated microglial activation and elevated synaptic protein levels in the hippocampus. These findings suggest that B. breve MCC1274 may mitigate AD-like pathologies in WT mice by decreasing Aβ42 levels, inhibiting tau phosphorylation, attenuating neuroinflammation, and improving synaptic protein levels.
Insights
Bifidobacterium breve MCC1274 (B. breve MCC1274) supplementation in wild-type mice reduced Alzheimer's disease-like pathologies. This probiotic may mitigate neuroinflammation and improve synaptic function, offering potential benefits for brain health.
Area of Science:
- Neuroscience
- Microbiology
- Gastroenterology
Background:
- Probiotics influence brain function through the microbiome-gut-brain axis.
- Bifidobacterium breve MCC1274 (B. breve MCC1274) has shown cognitive benefits and mitigation of Alzheimer's disease (AD)-like pathologies in specific models.
- The effects of B. breve MCC1274 on wild-type (WT) mice relevant to AD pathology were previously unexplored.
Purpose of the Study:
- To investigate the impact of B. breve MCC1274 on AD-like pathologies in two-month-old WT mice.
- To evaluate the effects of long-term oral administration of B. breve MCC1274 on key AD biomarkers and neuroinflammatory markers.
Main Methods:
- WT mice were orally administered B. breve MCC1274 for four months.
- Evaluated parameters included amyloid-beta (Aβ) levels, amyloid precursor protein (APP) processing, phosphorylated tau, synaptic proteins, glial activity, and cell proliferation.
- Statistical analysis involved Student's t-test and Shapiro-Wilk test for normality.
Main Results:
- Oral B. breve MCC1274 administration decreased soluble hippocampal Aβ42 levels by reducing presenilin1 protein.
- Phosphorylated tau levels were reduced, potentially via activation of the Akt/GSK-3β pathway.
- Microglial activation was attenuated, and hippocampal synaptic protein levels were elevated.
Conclusions:
- B. breve MCC1274 may mitigate AD-like pathologies in WT mice.
- The probiotic appears to reduce Aβ42 levels and tau phosphorylation.
- Findings suggest B. breve MCC1274 attenuates neuroinflammation and enhances synaptic function.
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