LiCl attenuates impaired learning and memory of APP/PS1 mice, which in mechanism involves α7 nAChRs and Wnt/β‐catenin pathway. Issue 22 (28th October 2021)

• Record Type: Journal Article
• Authors: Xiang, Jie; Ran, Long‐Yan; Zeng, Xiao‐Xiao; He, Wen‐Wen; Xu, Yi; Cao, Kun; Dong, Yang‐Ting; Qi, Xiao‐Lan; Yu, Wen‐Feng; Xiao, Yan; Guan, Zhi‐Zhong
• Is Part Of: Journal of cellular and molecular medicine. Volume 25:Issue 22(2021)
• Page Start: 10698
• Page End: 10710
• Publication Date: 2021-10-28
• Subjects: APP/PS1 mice -- AβOs -- LiCl -- Wnt/β‐catenin signalling pathway -- α7 nAChR; Cytology; Medicine; Molecular Biology; Cytologie -- Périodiques; Médecine -- Périodiques; Biologie moléculaire -- Périodiques; Cytology -- Periodicals; Medicine -- Periodicals; Molecular biology -- Periodicals; 611.01805
• DOI: 10.1111/jcmm.17006
• Languages: English
• ISSNs: 1582-1838

Abstract

Abstract: We examined the mechanism by which lithium chloride (LiCl) attenuates the impaired learning capability and memory function of dual‐transgenic APP/PS1 mice. Six‐ or 12‐month‐old APP/PS1 and wild‐type (WT) mice were randomized into four groups, namely WT, WT+Li (100 mg LiCl/kg body weight, gavage once daily), APP/PS1 and APP/PS1+Li. Primary rat hippocampal neurons were exposed to β‐amyloid peptide oligomers (AβOs), LiCl and/or XAV939 (inhibitor of Wnt/β‐catenin) or transfected with small interfering RNA against the β‐catenin gene. In the cerebral zone of APP/PS1 mice, the level of Aβ was increased and those of α7 nicotinic acetylcholine receptors (nAChR), phosphor‐GSK3β (ser9), β‐catenin and cyclin D1 (protein and/or mRNA levels) reduced. Two‐month treatment with LiCl at ages of 4 or 10 months weakened all of these effects. Similar expression variations were observed for these proteins in primary neurons exposed to AβOs, and these effects were attenuated by LiCl and aggravated by XAV939. Inhibition of β‐catenin expression lowered the level of α7 nAChR protein in these cells. LiCl attenuates the impaired learning capability and memory function of APP/PS1 mice via a mechanism that might involve elevation of the level of α7 nAChR as a result of altered Wnt/β‐catenin signalling.