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雄性和雌性 Fmr1 基因敲除小鼠(背景为 C57 白化鼠)表现出空间学习和记忆损伤。

Male and female Fmr1 knockout mice on C57 albino background exhibit spatial learning and memory impairments.

机构信息

Neuroscience Research, Lexicon Pharmaceuticals Inc., The Woodlands, TX 77381-1160, USA.

出版信息

Genes Brain Behav. 2010 Aug;9(6):562-74. doi: 10.1111/j.1601-183X.2010.00585.x. Epub 2010 Apr 6.

Abstract

Impaired spatial learning is a prominent deficit in fragile X syndrome (FXS). Previous studies using the Fmr1 knockout (KO) mouse model of FXS have not consistently reported a deficit in spatial learning. Fmr1 KO mice bred onto an albino C57BL/6J-Tyr(c-Brd) background showed significant deficits in several primary measures of performance during place navigation and probe trials in the Morris water maze. Fmr1 KO mice were also impaired during a serial reversal version of the water maze task. We examined fear conditioning as an additional cognitive screen. Knockout mice exhibited contextual memory deficits when trained with unsignaled shocks; however, deficits were not found in a separate group of KO mice trained with signaled shocks. No potentially confounding genotypic differences in locomotor activity were observed. A decreased anxiety-like profile was apparent in the open field, as others have noted, and also in the platform test. Also as previously reported, startle reactivity to loud auditory stimuli was decreased, prepulse inhibition and social interaction increased in KO mice. Female Fmr1 KO mice were tested along with male KO mice in all assays, except for social interaction. The female and male KO exhibited very similar impairments indicating that sex does not generally drive the behavioral symptoms of the disorder. Our results suggest that procedural factors, such as the use of albino mice, may help to reliably detect spatial learning and memory impairments in both sexes of Fmr1 KO mice, making it more useful for understanding FXS and a platform for evaluating potential therapeutics.

摘要

空间学习障碍是脆性 X 综合征 (FXS) 的一个突出缺陷。先前使用 FXS 的 Fmr1 敲除 (KO) 小鼠模型的研究并未一致报告空间学习缺陷。在几种主要的行为表现测量中,Fmr1 KO 小鼠在莫里斯水迷宫中的位置导航和探针试验中表现出显著缺陷,这些小鼠是在白化 C57BL/6J-Tyr(c-Brd) 背景下繁殖的。Fmr1 KO 小鼠在水迷宫任务的连续反转版本中也受到损害。我们将恐惧条件作为另一种认知筛选方法进行了检查。在未标记的电击条件下训练时,敲除小鼠表现出明显的情景记忆缺陷;然而,在另一组接受标记电击训练的 KO 小鼠中并未发现这种缺陷。没有观察到潜在的混淆基因型差异在运动活性中。与其他人的报道一样,在开阔场和平台试验中,敲除小鼠的焦虑样特征明显减少。如前所述,对大声听觉刺激的惊跳反应减少,KO 小鼠的前脉冲抑制和社会互动增加。除了社会互动,所有的检测都包括雌性和雄性 KO 小鼠,除了社会互动。雌性和雄性 KO 表现出非常相似的损伤,表明性别通常不会导致该疾病的行为症状。我们的研究结果表明,程序因素,如白化小鼠的使用,可能有助于可靠地检测 Fmr1 KO 小鼠两性的空间学习和记忆损伤,使其更有助于理解 FXS 并成为评估潜在治疗方法的平台。

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