Oral Administration of Bifidobacterium lactis Ameliorates Cognitive Deficits in Mice Intracerebroventricularly Administered Amyloid Beta via Regulation the Activation of Mitogen-activated Protein Kinases.
Jong Kyu ChoiOh Yun KwonSeung Ho LeePublished in: Food science of animal resources (2024)
Probiotics are functional microorganisms that exhibit various biological activities, such as allergic reactions, inflammation, and aging. The aim of this study is to evaluate the effects of Bifidobacterium lactis CBT BL3 (BL) on the amyloid beta (Aβ)-mediated cognitive impairments. Oral administration of live BL to intracerebroventricularly Aβ-injected mice significantly attenuated short- and long-term memory loss estimated using the Y-maze and Morris water maze tests. We found that expression of apoptosis-related proteins such as caspase-9, caspase-3, and cleaved poly (ADP-ribose) polymerase was significantly elevated in the brain tissues of Aβ-injected mouse brains when compared to that of the control mouse group. Interestingly, these expression levels were significantly decreased in the brain tissue of mice fed BL for 6 wk. In addition, the abnormal over-phosphorylation of mitogen-activated protein kinases (MAPKs) such as ERK1/2, p38 MAPK, and JNK in the brain tissue of intracerebroventricularly Aβ-injected mice was significantly attenuated by oral administration of BL. Taken together, the results indicate that Aβ-induced cognitive impairment may be ameliorated by the oral administration of BL by controlling the activation of MAPKs/apoptosis in the brain. This study strongly suggests that BL can be developed as a functional probiotic to attenuate Aβ-mediated cognitive deficits.
Keyphrases
- cell death
- resting state
- high fat diet induced
- oxidative stress
- white matter
- poor prognosis
- cognitive impairment
- endoplasmic reticulum stress
- induced apoptosis
- functional connectivity
- signaling pathway
- cell cycle arrest
- cerebral ischemia
- gene expression
- type diabetes
- insulin resistance
- cell proliferation
- multiple sclerosis
- wild type
- mouse model
- metabolic syndrome
- skeletal muscle
- long non coding rna
- endothelial cells
- drug induced
- high glucose