Dejean Camille, Dupont Typhaine, Verpy Elisabeth, Gonçalves Noémi, Coqueran Sabrina, Michalski Nicolas, Pucheu Sylvie, Bourgeron Thomas, Gourévitch Boris
Institut Pasteur, Université Paris Cité, INSERM, Institut de l'Audition, Plasticity of Central Auditory Circuits, F-75012 Paris, France.
Cilcare Company, F-34080 Montpellier, France.
Brain Sci. 2023 Oct 31;13(11):1539. doi: 10.3390/brainsci13111539.
Mice are increasingly used as models of human-acquired neurological or neurodevelopmental conditions, such as autism, schizophrenia, and Alzheimer's disease. All these conditions involve central auditory processing disorders, which have been little investigated despite their potential for providing interesting insights into the mechanisms behind such disorders. Alterations of the auditory steady-state response to 40 Hz click trains are associated with an imbalance between neuronal excitation and inhibition, a mechanism thought to be common to many neurological disorders. Here, we demonstrate the value of presenting click trains at various rates to mice with chronically implanted pins above the inferior colliculus and the auditory cortex for obtaining easy, reliable, and long-lasting access to subcortical and cortical complex auditory processing in awake mice. Using this protocol on a mutant mouse model of autism with a defect of the gene, we show that the neural response is impaired at high click rates (above 60 Hz) and that this impairment is visible subcortically-two results that cannot be obtained with classical protocols for cortical EEG recordings in response to stimulation at 40 Hz. These results demonstrate the value and necessity of a more complete investigation of central auditory processing disorders in mouse models of neurological or neurodevelopmental disorders.
小鼠越来越多地被用作人类获得性神经或神经发育疾病的模型,如自闭症、精神分裂症和阿尔茨海默病。所有这些疾病都涉及中枢听觉处理障碍,尽管它们有可能为深入了解此类障碍背后的机制提供有趣的见解,但目前对此研究甚少。对40赫兹短声序列的听觉稳态反应改变与神经元兴奋和抑制之间的失衡有关,这种机制被认为是许多神经疾病所共有的。在这里,我们展示了以不同速率向在下丘和听觉皮层上方长期植入电极的小鼠呈现短声序列的价值,以便在清醒小鼠中轻松、可靠且持久地获取皮层下和皮层复杂听觉处理信息。在一种具有基因缺陷的自闭症突变小鼠模型上使用该方案,我们发现高短声速率(高于60赫兹)时神经反应受损,并且这种损伤在皮层下可见——这两个结果是传统的用于记录40赫兹刺激下皮层脑电图的方案无法获得的。这些结果证明了在神经或神经发育障碍小鼠模型中更全面地研究中枢听觉处理障碍的价值和必要性。