首页> 美国卫生研究院文献>The Journal of Neuroscience >Altered Auditory Processing Filtering and Reactivity in the Cntnap2 Knock-Out Rat Model for Neurodevelopmental Disorders
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Altered Auditory Processing Filtering and Reactivity in the Cntnap2 Knock-Out Rat Model for Neurodevelopmental Disorders

机译:Cntnap2基因敲除大鼠模型中神经发育障碍的改变听觉处理筛选和反应性。

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摘要

Sensory processing, and auditory processing in particular, is altered in individuals with neurodevelopmental disorders such as autism spectrum disorders (ASDs). The typical maturation of the auditory system is perturbed in these individuals during early development, which may underlie altered auditory reactivity that persists in later life. Of the many genes that regulate the auditory system development, loss-of-function mutations in the CNTNAP2 gene are strongly associated with language processing deficits and ASD. Therefore, using a novel Cntnap2 knock-out rat model, we tested the impact of Cntnap2 loss on auditory processing, filtering, and reactivity throughout development and young adulthood in male and female animals. Although hearing thresholds were not altered in Cntnap2 knock-out animals, we found a reduction in response amplitudes and a delay in response latency of the auditory brainstem response (ABR) in juvenile Cntnap2 knock-out rats compared with age-matched controls. Amplitudes and latency of the ABR largely normalized by adulthood, indicating a delayed maturation of auditory processing pathways in Cntnap2 knock-out rats. Despite the reduced ABR amplitudes, adolescent Cntnap2 knock-out animals displayed increased startle reactivity accompanied by disruptions in sensory filtering and sensorimotor gating across various conditions, most of which persisted in adulthood. All of these observations show striking parallels to disruptions reported in ASD. Our results also imply that developmental disruptions of sensory signal processing are associated with persistent changes in neural circuitries responsible for implicit auditory evoked behavior, emphasizing the need for interventions that target sensory processing disruptions early during development in ASD.>SIGNIFICANCE STATEMENT This is the first study of brainstem auditory processing in a novel knock-out rat model with very high construct and face validity for autism spectrum disorders. Electrophysiological and behavioral measures of implicit auditory-evoked responses were systematically taken across developmental stages. Auditory processing, filtering, and reactivity disruptions show striking similarities to observations in autism. We also show for the first time that, whereas auditory brainstem responses normalize by adulthood, disruptions in brainstem-mediated auditory-evoked behavior persist. This indicates that early developmental perturbations in sensory processing can cause permanent maladaptive changes in circuitries responsible for auditory reactivity, underlining the importance for interventions early during development aiming at normalizing sensory processing.
机译:患有神经发育障碍(例如自闭症谱系障碍(ASD))的个体的感觉处理(尤其是听觉处理)会发生变化。这些个体在早期发育过程中会受到听觉系统的典型成熟困扰,这可能是改变的听觉反应性的基础,并在以后的生活中持续存在。在调节听觉系统发育的许多基因中,CNTNAP2基因的功能丧失突变与语言加工缺陷和ASD密切相关。因此,使用新型的Cntnap2基因敲除大鼠模型,我们测试了Cntnap2缺失对雄性和雌性动物整个发育和成年后的听觉加工,过滤和反应性的影响。尽管在Cntnap2基因敲除动物中听阈没有改变,但我们发现与年龄相匹配的对照组相比,在幼年Cntnap2基因敲除大鼠中反应幅度降低和听觉脑干反应(ABR)的反应潜伏期延迟。成年期的ABR的幅度和潜伏期在很大程度上已成年,这表明Cntnap2基因敲除大鼠的听觉加工途径的延迟成熟。尽管降低了ABR幅度,但青春期Cntnap2敲除动物表现出惊吓的反应性,并伴随着各种条件下感觉过滤和感觉运动门控的中断,其中大多数持续到成年。所有这些观察结果都显示出与ASD中报告的中断有惊人的相似之处。我们的研究结果还暗示,感觉信号处理的发展中断与负责隐性听觉诱发行为的神经回路的持续变化有关,强调需要针对ASD发育早期感觉处理中断的干预措施。>意义声明 >这是首次在新颖的基因敲除大鼠模型中对脑干听觉处理进行的研究,该模型具有很高的结构和对自闭症谱系障碍的面部有效性。隐性听觉诱发反应的电生理和行为措施是跨发育阶段系统地采取的。听觉处理,过滤和反应性中断显示出与自闭症中观察到的惊人相似之处。我们还首次表明,尽管成年期听觉脑干反应正常化,但脑干介导的听觉诱发行为的破坏仍持续存在。这表明感觉处理过程中的早期发育扰动会导致负责听觉反应性的电路发生永久性适应不良变化,从而突显了在发育过程中旨在使感觉处理正常化的早期干预措施的重要性。

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