Suppr超能文献

携带突变淀粉样前体蛋白和早老素-1转基因的转基因小鼠中与年龄相关的进行性行为障碍。

Progressive, age-related behavioral impairments in transgenic mice carrying both mutant amyloid precursor protein and presenilin-1 transgenes.

作者信息

Arendash G W, King D L, Gordon M N, Morgan D, Hatcher J M, Hope C E, Diamond D M

机构信息

Alzheimer's Research Laboratory, Department of Biology, University of South Florida, Tampa, FL 33620, USA.

出版信息

Brain Res. 2001 Feb 9;891(1-2):42-53. doi: 10.1016/s0006-8993(00)03186-3.

Abstract

This study provides a comprehensive behavioral characterization during aging of transgenic mice bearing both presenilin-1 (PS1) and amyloid precursor protein (APP(670,671)) mutations. Doubly transgenic mice and non-transgenic controls were evaluated at ages wherein beta-amyloid (Abeta) neuropathology in APP+PS1 mice is low (5-7 months) or very extensive (15-17 months). Progressive cognitive impairment was observed in transgenic mice for both water maze acquisition and radial arm water maze working memory. However, transgenicity did not affect Y-maze alternations, circular platform performance, standard water maze retention, or visible platform recognition at either age, nor did transgenicity affect anxiety levels in elevated plus-maze testing. In sensorimotor tasks, transgenic mice showed a progressive increase in open field activity, a progressive impairment in string agility, and an early-onset impairment in balance beam. None of these sensorimotor changes appeared to be contributory to any cognitive impairments observed, however. Non-transgenic mice showed no progressive behavioral change in any measure evaluated. Given the age-related cognitive impairments presently observed in APP+PS1 transgenic mice and their progressive Abeta deposition/neuroinflammation, Abeta neuropathology could be involved in these progressive cognitive impairments. As such, the APP+PS1 transgenic mouse offers unique opportunities to develop therapeutics to treat or prevent Alzheimer's Disease through modulation of Abeta deposition/neuroinflammation.

摘要

本研究对携带早老素-1(PS1)和淀粉样前体蛋白(APP(670,671))突变的转基因小鼠衰老过程中的行为特征进行了全面描述。对双转基因小鼠和非转基因对照小鼠在APP+PS1小鼠中β-淀粉样蛋白(Aβ)神经病理学程度较低(5-7个月)或非常广泛(15-17个月)的年龄进行了评估。在水迷宫获取和放射状臂水迷宫工作记忆方面,转基因小鼠均出现了进行性认知障碍。然而,转基因在两个年龄段均未影响Y迷宫交替、圆形平台表现、标准水迷宫记忆或可视平台识别,在高架十字迷宫测试中也未影响焦虑水平。在感觉运动任务中,转基因小鼠在旷场活动中表现出进行性增加,在绳梯敏捷性方面出现进行性损伤,在平衡木上出现早期损伤。然而,这些感觉运动变化似乎都与所观察到的任何认知障碍无关。非转基因小鼠在任何评估指标中均未表现出进行性行为变化。鉴于目前在APP+PS1转基因小鼠中观察到的与年龄相关的认知障碍及其进行性Aβ沉积/神经炎症,Aβ神经病理学可能与这些进行性认知障碍有关。因此,APP+PS1转基因小鼠为通过调节Aβ沉积/神经炎症来开发治疗或预防阿尔茨海默病的疗法提供了独特的机会。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验