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脑源性多巴胺神经营养因子可改善阿尔茨海默病模型APP/PS1转基因小鼠以及野生型小鼠的长期记忆。

Cerebral dopamine neurotrophic factor improves long-term memory in APP/PS1 transgenic mice modeling Alzheimer's disease as well as in wild-type mice.

作者信息

Kemppainen Susanna, Lindholm Päivi, Galli Emilia, Lahtinen Hanna-Maija, Koivisto Henna, Hämäläinen Elina, Saarma Mart, Tanila Heikki

机构信息

A.I. Virtanen Institute, University of Eastern Finland, Kuopio, Finland.

Institute of Biotechnology, University of Helsinki, Finland.

出版信息

Behav Brain Res. 2015 Sep 15;291:1-11. doi: 10.1016/j.bbr.2015.05.002. Epub 2015 May 11.

Abstract

Cerebral dopamine neurotrophic factor (CDNF) protects and repairs dopamine neurons in animal models of Parkinson's disease, which motivated us to investigate its therapeutic effect in an animal model of Alzheimer's disease (AD). We employed an established APP/PS1 mouse model of AD and gave intrahippocampal injections of CDNF protein or CDNF transgene in an AAV2 viral vector to 1-year-old animals. We performed a behavioral test battery 2 weeks after the injections and collected tissue samples after the 3-week test period. Intrahippocampal CDNF-therapy improved long-term memory in both APP/PS1 mice and wild-type controls, but did not affect spontaneous exploration, object neophobia or early stages of spatial learning. The memory improvement was not associated with decreased brain amyloid load or enhanced hippocampal neurogenesis. Intracranial CDNF treatment has beneficial effects on long-term memory and is well tolerated. The CDNF molecular mechanisms of action on memory await further studies.

摘要

脑源性多巴胺神经营养因子(CDNF)在帕金森病动物模型中可保护和修复多巴胺能神经元,这促使我们研究其在阿尔茨海默病(AD)动物模型中的治疗效果。我们采用了已建立的AD的APP/PS1小鼠模型,并向1岁的动物海马内注射CDNF蛋白或携带CDNF转基因的AAV2病毒载体。注射后2周我们进行了一系列行为测试,并在3周的测试期后收集组织样本。海马内CDNF治疗改善了APP/PS1小鼠和野生型对照的长期记忆,但不影响自发探索、物体新恐惧症或空间学习的早期阶段。记忆改善与脑淀粉样蛋白负荷降低或海马神经发生增强无关。颅内CDNF治疗对长期记忆有有益影响且耐受性良好。CDNF对记忆的分子作用机制有待进一步研究。

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