Honokiol improves cognitive impairment in APP/PS1 mice through activating mitophagy and mitochondrial unfolded protein response

被引:41
作者
Hou, Mingyue [1 ]
Bao, Wenfang [1 ]
Gao, Yuanyuan [1 ]
Chen, Jiayue [1 ]
Song, Guijun [1 ]
机构
[1] Dalian Med Univ, Dept Neurol, Hosp 2, 467 Zhongshan Rd, Dalian 116027, Liaoning, Peoples R China
关键词
Honokiol; Alzheimer's disease; Mitophagy; UPRmt; SIRT3; QUALITY-CONTROL; AMYLOID-BETA; DYSFUNCTION; BIOGENESIS; UPRMT;
D O I
10.1016/j.cbi.2021.109741
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activated mitophagy and mitochondrial unfolded protein response (UPRmt) has been reported to protect against mitochondrial dysfunction, which is closely related to the onset of Alzheimer's disease (AD). Honokiol (HKL, C18H18O2) is a kind of natural extraction from bark of Magnolia officinalis with anti-AD effect, and our study aims to explore the effect of HKL on mitophagy and UPRmt in AD. Briefly, male APP/PS1 mice and A beta oligmer (A beta O)treated primary hippocampal neurons were respectively used to mimic AD in vivo and in vitro. It was determined that HKL significantly ameliorated cognitive impairment and synaptic damages in APP/PS1 mice. Besides, the activated mitophagy and UPRmt together with inhibited oxidative stress and improved mitochondrial dynamic disorder were further validated in hippocampus of HKL-treated APP/PS1 mice. Meanwhile, HKL-treated mice displayed much higher hippocampal expression and activity of mitochondrial sirtuin 3 (SIRT3). Therefore, SIRT3 knockdown was further achieved in primary hippocampal neurons by effective shRNA, and we determined that HKL improved synaptic damage, mitochondrial dysfunction, mitophagy and UPRmt in A beta O-treated primary hippocampal neurons in a SIRT3-dependent manner. In summary, our study validates the protective effect of HKL on AD, and highlights that HKL exerts anti-AD effect by activating mitophagy and UPRmt.
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页数:13
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