自噬
神经退行性变
蛋白激酶B
衰老
PI3K/AKT/mTOR通路
认知功能衰退
衰老的大脑
生物
下调和上调
FOXO3公司
神经科学
细胞生物学
内分泌学
信号转导
内科学
医学
认知
细胞凋亡
生物化学
基因
痴呆
疾病
作者
Min Fu,Xiaoshan Liang,Xuguang Zhang,Mingzhe Yang,Ye Qi,Yuxuan Qi,Huan Liu,Xumei Zhang
标识
DOI:10.1080/1028415x.2022.2055376
摘要
Brain aging is a complex biological process often associated with a decline in cognitive functions and motility. Astaxanthin (AST) is a strong antioxidant capable of crossing the blood-brain barrier. The effect of AST on brain aging and its physiological and molecular mechanism are still unclear. The study aimed to investigate whether AST from AstaReal A1010 improved brain aging by inducing autophagy in SAMP10 mice. Different concentrations of AstaReal A1010 were intragastrically administered to 6-month-old SAMP10 mice for 3 months. The results demonstrated that AST delayed age-related cognitive decline, motor ability and neurodegeneration, upregulated the expression levels of autophagy-related genes beclin-1 and LC3 in the brain. It may induce autophagy by regulating IGF-1/Akt/mTOR and IGF-1/Akt/FoxO3a signaling. Treatment with autophagy inhibitor 3-methyladenine (3MA) partly reversed the anti-aging effect of AST. In conclusion, our findings suggest that AST may induce autophagy by regulating IGF-1/Akt/mTOR and IGF-1/Akt/FoxO3a signaling, thereby delaying age-related neurodegeneration and cognitive decline in SAMP10 mice.
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