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脆性X综合征大鼠模型中的语音退化处理

Degraded speech sound processing in a rat model of fragile X syndrome.

作者信息

Engineer Crystal T, Centanni Tracy M, Im Kwok W, Rahebi Kimiya C, Buell Elizabeth P, Kilgard Michael P

机构信息

School of Behavioral and Brain Sciences, The University of Texas at Dallas, 800 West Campbell Road GR41, Richardson, TX 75080, United States.

School of Behavioral and Brain Sciences, The University of Texas at Dallas, 800 West Campbell Road GR41, Richardson, TX 75080, United States.

出版信息

Brain Res. 2014 May 20;1564:72-84. doi: 10.1016/j.brainres.2014.03.049. Epub 2014 Apr 5.

Abstract

Fragile X syndrome is the most common inherited form of intellectual disability and the leading genetic cause of autism. Impaired phonological processing in fragile X syndrome interferes with the development of language skills. Although auditory cortex responses are known to be abnormal in fragile X syndrome, it is not clear how these differences impact speech sound processing. This study provides the first evidence that the cortical representation of speech sounds is impaired in Fmr1 knockout rats, despite normal speech discrimination behavior. Evoked potentials and spiking activity in response to speech sounds, noise burst trains, and tones were significantly degraded in primary auditory cortex, anterior auditory field and the ventral auditory field. Neurometric analysis of speech evoked activity using a pattern classifier confirmed that activity in these fields contains significantly less information about speech sound identity in Fmr1 knockout rats compared to control rats. Responses were normal in the posterior auditory field, which is associated with sound localization. The greatest impairment was observed in the ventral auditory field, which is related to emotional regulation. Dysfunction in the ventral auditory field may contribute to poor emotional regulation in fragile X syndrome and may help explain the observation that later auditory evoked responses are more disturbed in fragile X syndrome compared to earlier responses. Rodent models of fragile X syndrome are likely to prove useful for understanding the biological basis of fragile X syndrome and for testing candidate therapies.

摘要

脆性X综合征是最常见的遗传性智力障碍形式,也是自闭症的主要遗传病因。脆性X综合征中语音处理受损会干扰语言技能的发展。尽管已知脆性X综合征患者的听觉皮层反应异常,但尚不清楚这些差异如何影响语音处理。本研究首次证明,尽管Fmr1基因敲除大鼠的语音辨别行为正常,但其语音的皮层表征仍受损。在初级听觉皮层、前听觉场和腹侧听觉场中,对语音、噪声突发序列和纯音的诱发电位和放电活动显著降低。使用模式分类器对语音诱发活动进行神经计量分析证实,与对照大鼠相比,Fmr1基因敲除大鼠这些区域的活动包含的关于语音身份的信息显著减少。与声音定位相关的后听觉场反应正常。在与情绪调节相关的腹侧听觉场中观察到最大程度的损伤。腹侧听觉场功能障碍可能导致脆性X综合征患者情绪调节不佳,这或许有助于解释为什么与早期反应相比,脆性X综合征患者后期的听觉诱发反应受到的干扰更大。脆性X综合征的啮齿动物模型可能有助于理解脆性X综合征的生物学基础,并用于测试候选疗法。

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