Anandamide and noladin ether prevent neurotoxicity of the human amyloid-β peptide

被引:100
作者
Milton, NGN [1 ]
机构
[1] UCL Royal Free & Univ Coll, Sch Med, Dept Mol Pathol & Clin Biochem, London NW3 2PF, England
关键词
amyloid-beta; noladin ether; anandamide; cannabinoid; mitogen activated protein kinase; neurons; Alzheimer's; corticotrophin-releasing hormone;
D O I
10.1016/S0304-3940(02)00936-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cannabinoid receptor agonists including anandamide and noladin ether have recently been suggested to exhibit neuroprotective properties. The amyloid-beta (Abeta) peptide is thought to be responsible for the neurodegenerative changes associated with Alzheimer's disease pathology. This study characterizes the effects of anandamide and noladin ether on the neurotoxicity of Abeta in differentiated human teratocarcinoma cell line, Ntera 2/cl-D1 neurons. Anandamide and noladin ether, at nanomolar concentrations, showed concentration dependent inhibition of Abeta toxicity. A CB1 cannabinoid receptor antagonist, AM251, prevented the protective effects of anandamide and noladin ether. The mitogen activated protein kinase (MAPK) pathway inhibitor PD98059 also prevented the protective effects of cannabinoids and corticotrophin-releasing hormone. These results suggest that activation of the MAPK pathway by either cannabinoids or corticotrophin-releasing hormone could be used to prevent Abeta peptide induced neurodegeneration. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:127 / 130
页数:4
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