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西普西凡,一种 H3 受体拮抗剂,可缓解阿尔茨海默病 APP Tg2576 小鼠模型的多动和认知缺陷。

Ciproxifan, an H3 receptor antagonist, alleviates hyperactivity and cognitive deficits in the APP Tg2576 mouse model of Alzheimer's disease.

机构信息

Department of Psychological Science, Northern Kentucky University, 1 Nunn Drive, Highland Heights, KY 41076, USA.

出版信息

Neurobiol Learn Mem. 2011 Jan;95(1):64-72. doi: 10.1016/j.nlm.2010.10.008. Epub 2010 Nov 10.

Abstract

Previous research has indicated that the blockade of H(3)-type histamine receptors may improve attention and memory in normal rodents. The purpose of this study was to determine if ciproxifan, an H(3) receptor antagonist, could alleviate the hyperactivity and cognitive deficits observed in a transgenic mouse model (APP(Tg2576)) of Alzheimer's disease. APP(Tg2576) mice displayed significantly greater locomotor activity than wild-type mice, but APP(Tg2576) mice provided with daily ciproxifan treatment showed activity levels that did not differ from wild-type mice. In the swim maze, APP(Tg2576) mice exhibited significantly longer escape latencies, but the APP(Tg2576) mice treated daily with ciproxifan had latencies that were indistinguishable from controls. In probe trials conducted one hour after the last training trial, ciproxifan-treated APP(Tg2576) mice spent more time near the previous platform location and made more crossings of this area than did saline-treated APP(Tg2576) mice. APP(Tg2576) mice also demonstrated a significant impairment in the object recognition task that was reversed by acute treatment with ciproxifan (3.0mg/kg). These data support the idea that modulation of H(3) receptors represents a novel and viable therapeutic strategy in the treatment of Alzheimer's disease.

摘要

先前的研究表明,阻断 H(3) 型组胺受体可能改善正常啮齿动物的注意力和记忆力。本研究的目的是确定 H(3) 受体拮抗剂西替利嗪是否能减轻阿尔茨海默病转基因小鼠模型(APP(Tg2576)) 中观察到的多动和认知缺陷。APP(Tg2576) 小鼠的运动活性明显高于野生型小鼠,但接受西替利嗪每日治疗的 APP(Tg2576) 小鼠的活性水平与野生型小鼠无差异。在游泳迷宫中,APP(Tg2576) 小鼠表现出明显更长的逃避潜伏期,但接受西替利嗪每日治疗的 APP(Tg2576) 小鼠的潜伏期与对照组无法区分。在最后一次训练试验后一小时进行的探测试验中,接受西替利嗪治疗的 APP(Tg2576) 小鼠在先前平台位置附近停留的时间更长,穿过该区域的次数也更多。APP(Tg2576) 小鼠在物体识别任务中也表现出明显的损伤,而急性西替利嗪(3.0mg/kg)治疗可逆转这种损伤。这些数据支持这样一种观点,即调节 H(3) 受体代表了治疗阿尔茨海默病的一种新颖且可行的治疗策略。

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