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Steroid-Enriched Fraction of Achyranthes bidentata Protects Amyloid β Peptide 1–40-Induced Cognitive Dysfunction and Neuroinflammation in Rats.

Authors :
Lin, Li-Wei
Tsai, Fan-Hsuan
Lan, Wan-Cheng
Cheng, Yih-Dih
Lee, Sheng-Chi
Wu, Chi-Rei
Source :
Molecular Neurobiology; Aug2019, Vol. 56 Issue 8, p5671-5688, 18p
Publication Year :
2019

Abstract

The roots of Achyranthes bidentata Blume (AB) is commonly used in the treatment of osteoporosis and dementia in traditional Chinese medicine. Pharmacological reports evidenced that AB possessed anti-osteoarthritis effects. However, there is little literature about the anti-dementia activities of AB. The present study was designed to prepare steroid-enriched fraction of AB (ABS) and investigate whether ABS can protect from cognitive dysfunction and neuroinflammation against Aβ 1–40-induced Alzheimer's disease (AD) model in rats. ABS only contained 135.11 ± 4.28 mg of ecdysterone per gram. ABS (50 mg/kg) reversed the dysfunction of exploratory activity and memory function on plus-maze and Morris water maze caused by Aβ 1–40 in rats. ABS (50 mg/kg) also decreased amyloid deposition, neurofibrillary tangle, neural damage, activated astrocyte, and microglial caused by Aβ 1–40. Furthermore, ABS reversed the phenomenon of neural oxidative damage and neuroinflammation, including the higher levels of MDA and cytokines, and the lower activities of antioxidant enzymes and GSH levels caused by Aβ 1–40 in rat cortex and hippocampus. Finally, ABS restored the activation of ERK pathway and decreased NF-κB phosphorylation and translocation altered by Aβ 1–40. ABS alone (50 mg/kg) promoted cognitive function, activated brain antioxidant defense system, and decreased brain TNF-α levels in sham group. Therefore, ABS has the cognition-promoting and antidementia potential. Steroids especial ecdysterone are major active components of AB. The action mechanism is due to decreasing oxidative stress and neuroinflammation through modulating ERK pathway, NF-κB phosphorylation, and translocation in Aβ 1–40-induced AD rat model. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08937648
Volume :
56
Issue :
8
Database :
Complementary Index
Journal :
Molecular Neurobiology
Publication Type :
Academic Journal
Accession number :
137399374
Full Text :
https://doi.org/10.1007/s12035-018-1436-7