Yifan Han

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Organization: The Hong Kong Polytechnic University , HongKong
Department: Department of Applied Biology and Chemistry Technology
Title: Professor(PhD)
Co-reporter:Ling Huang, Jiajia Lin, Siying Xiang, Kangrong Zhao, Jie Yu, Jiacheng Zheng, Daping Xu, Shinghung Mak, Shengquan Hu, Shehani Nirasha, Chuang Wang, Xiaowei Chen, Junfang Zhang, Shujun Xu, Xiaofei Wei, Zaijun Zhang, Dongsheng Zhou, Wenhua Zhou, Wei Cui, Yifan Han, Zhenyu Hu, and Qinwen Wang
ACS Chemical Neuroscience 2016 Volume 7(Issue 8) pp:1047
Publication Date(Web):April 5, 2016
DOI:10.1021/acschemneuro.5b00329
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.Keywords: AChE; Alzheimer’s disease; cancer; cognitive impairments; sunitinib
Su 4312;3-[[4-(dimethylamino)phenyl]methylene]-1,3-dihydro-2h-indol-2-one
1,7-Heptanediamine, N,N'-bis(1,2,3,4-tetrahydro-9-acridinyl)-
L-lactate dehydrogenase from rabbit muscle ~140 U/mg
2H-Indol-2-one, 3-[[4-(dimethylamino)phenyl]methylene]-1,3-dihydro-,(3Z)-
NEOSTIGMINE
5-(2-Aminoethyl)benzene-1,2,4-triol
(R,S)-AMPA
Cytochrome C
Ferrate(2-), [7,12-diethenyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(4-)-κN21,κN22,κN23,κN24]-, hydrogen (1:2), (SP-4-2)-
(2E,3E)-3-(Hydroxyimino)-[2,3'-biindolinylidene]-2'-one