Journal
FRONTIERS IN PHARMACOLOGY
Volume 10, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2019.01529
Keywords
beta-asarone; amyloid beta; Alzheimer's disease(AD); PC12; autophagy
Categories
Funding
- National Natural Science Foundation of China [81903971]
- General Program of China Postdoctoral Science Foundation [2018M643377]
- National Key R&D Program of China [2018YFC2002500]
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Alzheimer's disease (AD) is one of the most common types of dementia that causes memory, thinking, and behavior problems. The most important feature of AD is the gradual irreversible loss of cognitive ability through the formation of amyloid beta (A beta) plaques and neurofibrillary tangles composed of tau protein. The metabolism of A beta and tau proteins is closely related to and is affected by autophagy. Current research speculates that autophagy dysfunction leads to an increase in harmful proteins in AD. beta-Asarone is the main constituent of Acorus tatarinowii Schott and has important effects on the central nervous system. In this paper, we primarily explored the effects of beta-asarone on the clearance of noxious proteins and the associated potential mechanisms via autophagy in a PC12 cell AD model. A CCK-8 assay and LDH experiments were used to assess cell viability/toxicity, and SPiDER-beta Gal was used to detect cellular senescence. The important proteins associated with the pathogenesis of AD including APP, PS1, A beta, BACE1, and SYN1 were analyzed by immunofluorescence (IF) and Western blot analysis. Antimycin A (A3) and cyclosporine A (CSA) were selected as the activators and inhibitors of autophagy, respectively. LC3, BECN, P62, PINK1, and Parkin protein expression were also examined by IF and Western blot analysis. The data showed that beta-asarone administration significantly dose-dependently increased cell proliferation and decreased cytotoxicity; moreover, beta-asarone inhibited SA-beta Gal and improved cell senescence. The results further showed that, compared to the model, APP, PS1, A beta, BACE1, and p62 were reduced, while SYN1, BECN1, and LC3 were increased after treatment with beta-asarone. The results of Canonical Correlation Analysis (CCA) showed a highly significant relationship between the pathological factors of AD and the protein expression of autophagy. In conclusion, our study demonstrated that beta-asarone can inhibit A beta, and this effect may occur by promoting autophagy in a cell model of AD.
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