| Literature DB >> 27046396 |
Ling Huang1,2, Jiajia Lin1, Siying Xiang1, Kangrong Zhao1, Jie Yu1, Jiacheng Zheng1, Daping Xu3, Shinghung Mak3, Shengquan Hu3, Shehani Nirasha1, Chuang Wang1, Xiaowei Chen1, Junfang Zhang1, Shujun Xu1, Xiaofei Wei1, Zaijun Zhang4, Dongsheng Zhou2, Wenhua Zhou1, Wei Cui1, Yifan Han3, Zhenyu Hu2, Qinwen Wang1.
Abstract
Sunitinib, a tyrosine kinase inhibitor, is clinically used for the treatment of cancer. In this study, we found for the first time that sunitinib inhibits acetylcholinesterase (AChE) at submicromolar concentrations in vitro. In addition, sunitinib dramatically decreased the hippocampal and cortical activity of AChE in a time-dependent manner in mice. Molecular docking analysis further demonstrates that sunitinib might interact with both the catalytic anion and peripheral anionic sites within AChE, which is in accordance with enzymatic activity results showing that sunitinib inhibits AChE in a mixed pattern. Most importantly, we evaluated the effects of sunitinib on scopolamine-induced cognitive impairments in mice by using novel object recognition and Morris water maze tests. Surprisingly, sunitinib could attenuate cognitive impairments to a similar extent as donepezil, a marketed AChE inhibitor used for the treatment of Alzheimer's disease. In summary, our results have shown that sunitinib could potently inhibit AChE and attenuate cognitive impairments in mice.Entities:
Keywords: AChE; Alzheimer’s disease; cancer; cognitive impairments; sunitinib
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Year: 2016 PMID: 27046396 DOI: 10.1021/acschemneuro.5b00329
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418