Kelly P H, Bondolfi L, Hunziker D, Schlecht H-P, Carver K, Maguire E, Abramowski D, Wiederhold K-H, Sturchler-Pierrat C, Jucker M, Bergmann R, Staufenbiel M, Sommer B
NS Research, Novartis Pharma A.G. Ltd., CH-4002 Basel, Switzerland.
Neurobiol Aging. 2003 Mar-Apr;24(2):365-78. doi: 10.1016/s0197-4580(02)00098-2.
Transgenic APP23 mice expressing human APP(751) with the K670N/M671L mutation, were compared at ages 3, 18 or 25 months to non-transgenic littermates in passive avoidance and in a small and large Morris maze. The task in the smaller pool habituated their flight response to the platform. Impairments in passive avoidance and small pool performance in APP23 mice were clearly age-related. In the larger Morris maze APP23 mice at all ages were impaired in latency and distance swum before finding the platform. Identical performance of 18-month APP23 and controls in a visible platform condition indicates that the Morris maze performance deficit was not due to sensory, motor or motivational alterations. At age 3 months both groups initially unexpectedly avoided the visible platform, suggesting that in young mice neophobia may contribute significantly to performance in cognitive tests. In conclusion, APP23 mice exhibit both early behavioral impairment in the large Morris maze as well as impairments in passive avoidance and small pool performance that are marked only in old age.
将表达带有K670N/M671L突变的人APP(751)的转基因APP23小鼠,在3、18或25月龄时与非转基因同窝小鼠在被动回避以及小型和大型莫里斯迷宫实验中进行比较。在较小水池中的任务使它们对平台的逃避反应习惯化。APP23小鼠在被动回避和小型水池实验中的损伤明显与年龄相关。在大型莫里斯迷宫中,所有年龄的APP23小鼠在找到平台之前的潜伏期和游泳距离方面都存在损伤。18月龄的APP23小鼠和对照组在可见平台条件下表现相同,这表明莫里斯迷宫实验中的表现缺陷并非由于感觉、运动或动机改变所致。在3月龄时,两组最初都意外地避开了可见平台,这表明在幼鼠中,新事物恐惧症可能对认知测试的表现有显著影响。总之,APP23小鼠在大型莫里斯迷宫中表现出早期行为损伤,以及在被动回避和小型水池实验中的损伤,而这些损伤仅在老年时才明显。