福克斯O1
海马体
自噬
七氟醚
莫里斯水上航行任务
ATG5型
基因沉默
神经科学
医学
心理学
麻醉
生物
信号转导
细胞生物学
生物化学
细胞凋亡
蛋白激酶B
基因
作者
Yang Huifang,Zhao Li,Qin Li
摘要
Abstract The current study aimed to examine the effects of echinacoside on cognitive impairment in mice after exposure to sevoflurane. To examine the role of FOXO1, si‐FOXO1 and si‐con were injected into the hippocampus through the left lateral cerebral ventricles. Sevoflurane‐induced mice had serious cognitive dysfunction. However, pretreatment with echinacoside alleviated the cognitive dysfunction, as measured by a shortened escape latency time, and increased platform crossing times, the percentage of distance in the target quadrant and Y‐maze spontaneous alternations. In addition, we found that echinacoside elevated FOXO1 expression in the hippocampus; increased the expression of autophagy‐related proteins including Beclin 1, ATG5, ATG7, and LC3; and reduced P62 expression. Silencing of FOXO1 aggravated the cognitive deficits and reduced expression of the autophagy‐related markers, whereas the effects of si‐FOXO1 on memory were abrogated by echinacoside. Echinacoside attenuated the cognitive impairment in sevoflurane‐induced mice through FOXO1‐mediated autophagy.
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