β-Sitosterol treatment attenuates cognitive deficits and prevents amyloid plaque deposition in amyloid protein precursor/presenilin 1 mice
10.4196/kjpp.2020.24.1.39
- Author:
Jian Ya YE
1
;
Li LI
;
Qing Mao HAO
;
Yong QIN
;
Chang Sheng MA
Author Information
1. Hebei University of Chinese Medicine, Shijiazhang 050200, Hebei province, China.
- Publication Type:Original Article
- Keywords:
Alzheimer disease;
Amyloid-beta;
β-Sitosterol;
Learning and memory
- MeSH:
Alzheimer Disease;
Amyloid;
Animals;
Blood Platelets;
Blotting, Western;
Brain;
Cognition Disorders;
Dementia;
Dendritic Spines;
Enzyme-Linked Immunosorbent Assay;
Excitatory Postsynaptic Potentials;
Learning;
Memory;
Metabolism;
Mice;
Mice, Transgenic;
Neurodegenerative Diseases;
Neurons;
Neuroprotective Agents;
Plant Extracts;
Plants;
Plaque, Amyloid;
Spatial Learning
- From:The Korean Journal of Physiology and Pharmacology
2020;24(1):39-46
- CountryRepublic of Korea
- Language:English
-
Abstract:
Alzheimer's disease (AD) is the most common neurodegenerative disorder causing dementia worldwide, and is mainly characterized by aggregated β-amyloid (Aβ). Increasing evidence has shown that plant extracts have the potential to delay AD development. The plant sterol β-Sitosterol has a potential role in inhibiting the production of platelet Aβ, suggesting that it may be useful for AD prevention. In the present study, we aimed to investigate the effect and mechanism of β-Sitosterol on deficits in learning and memory in amyloid protein precursor/presenilin 1 (APP/PS1) double transgenic mice. APP/PS1 mice were treated with β-Sitosterol for four weeks, from the age of seven months. Brain Aβ metabolism was evaluated using ELISA and Western blotting. We found that β-Sitosterol treatment can improve spatial learning and recognition memory ability, and reduce plaque load in APP/PS1 mice. β-Sitosterol treatment helped reverse dendritic spine loss in APP/PS1 mice and reversed the decreased hippocampal neuron miniature excitatory postsynaptic current frequency. Our research helps to explain and support the neuroprotective effect of β-Sitosterol, which may offer a novel pharmaceutical agent for the treatment of AD. Taken together, these findings suggest that β-Sitosterol ameliorates memory and learning impairment in APP/PS1 mice and possibly decreases Aβ deposition.
