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Neurobehavioral deficits in the KIKO mouse model of Friedreich’s ataxia

机译:Friedreich共济失调的KIKO小鼠模型的神经行为缺陷

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摘要

Friedreich’s Ataxia (FA) is a pediatric neurodegenerative disease whose clinical presentation includes ataxia, muscle weakness, and peripheral sensory neuropathy. The KIKO mouse is an animal model of FA with frataxin deficiency first described in 2002, but neurobehavioral deficits have never been described in this model. The identification of robust neurobehavioral deficits in KIKO mice could support the testing of drugs for FA, which currently has no approved therapy. We tested 13 neurobehavioral tasks to identify a robust KIKO phenotype: Open Field, Grip Strength Test(s), Cylinder, Skilled Forelimb Grasp Task(s), Treadmill Endurance, Locotronic Motor Coordination, Inverted Screen, Treadscan, and Von Frey. Of these, Inverted Screen, Treadscan and Von Frey produced significant neurobehavioral deficits at >8 months of age, and relate to the clinically relevant endpoints of muscle strength and endurance, gait ataxia, and peripheral insensitivity. Thus we identify robust phenotypic measures related to Friedreich’s ataxia clinical endpoints which could be used to test effectiveness of potential drug therapy.
机译:Friedreich的共济失调(FA)是一种儿童神经退行性疾病,其临床表现包括共济失调,肌肉无力和周围感觉神经病。 KIKO小鼠是2002年首次描述的具有frataxin缺乏症的FA动物模型,但从未在该模型中描述过神经行为缺陷。 KIKO小鼠中强烈的神经行为缺陷的鉴定可以支持对FA的药物测试,目前尚无批准的疗法。我们测试了13种神经行为任务以识别稳健的KIKO表型:开阔地域,握力测试,圆柱体,熟练的前肢抓握任务,跑步机耐力,机车运动协调,倒置屏幕,跑步机和冯·弗雷。其中,倒置网眼,Treadscan和Von Frey在大于8个月大的时候会产生明显的神经行为缺陷,并且与临床上相关的肌肉力量和耐力,步态共济失调和外周不敏感有关。因此,我们确定了与Friedreich共济失调临床终点相关的可靠表型指标,可用于测试潜在药物疗法的有效性。

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