脆性X综合征大鼠模型中听觉特征辨别能力的改变。

Altered auditory feature discrimination in a rat model of Fragile X Syndrome.

作者信息

Gauthier D Walker, James Noelle, Auerbach Benjamin D

机构信息

Department of Molecular & Integrative Physiology, School of Molecular & Cellular Biology, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.

Beckman Institute for Advanced Science & Technology, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.

出版信息

PLoS Biol. 2025 Jul 1;23(7):e3003248. doi: 10.1371/journal.pbio.3003248. eCollection 2025 Jul.

Abstract

Atypical sensory processing, particularly in the auditory domain, is one of the most common and quality-of-life affecting symptoms seen in autism spectrum disorders (ASD). Fragile X Syndrome (FXS) is a leading inherited cause of ASD and a majority of FXS individuals present with auditory processing alterations. While auditory hypersensitivity is a common phenotype observed in FXS and Fmr1 knockout (KO) rodent models, it is important to consider other auditory coding impairments that could contribute to sound processing difficulties and disrupted language comprehension in FXS. We have shown previously that a Fmr1 KO rat model of FXS exhibits heightened sound sensitivity that coincided with abnormal perceptual integration of stimulus bandwidth, indicative of altered spectral processing. Frequency discrimination is a fundamental aspect of sound encoding that is important for a range of auditory processes, such as source segregation and speech comprehension, and disrupted frequency coding could thus contribute to a range of auditory issues in FXS and ASD. Here we explicitly characterized spectral processing deficits in male Fmr1 KO rats using an operant conditioning tone discrimination assay and in vivo electrophysiological recordings from the auditory cortex and inferior colliculus. We found that Fmr1 KO rats exhibited poorer frequency resolution, which corresponded with neuronal hyperactivity and broader frequency tuning in auditory cortical but not collicular neurons. Using an experimentally informed population model, we show that these cortical physiological differences can recapitulate the observed behavior discrimination deficits, with decoder performance being tightly linked to differences in cortical tuning width and signal-to-noise ratios. Together, these findings indicate that cortical hyperexcitability in Fmr1 KO rats may act to preserve signal-to-noise ratios and signal detection threshold at the expense of sound sensitivity and fine feature discrimination, highlighting a potential mechanistic locus for a range of auditory behavioral phenotypes in FXS.

摘要

非典型感觉加工,尤其是在听觉领域,是自闭症谱系障碍(ASD)中最常见且影响生活质量的症状之一。脆性X综合征(FXS)是ASD的主要遗传性病因,大多数FXS个体存在听觉加工改变。虽然听觉过敏是在FXS和Fmr1基因敲除(KO)啮齿动物模型中观察到的常见表型,但重要的是要考虑其他可能导致FXS声音加工困难和语言理解障碍的听觉编码损伤。我们之前已经表明,FXS的Fmr1 KO大鼠模型表现出声音敏感性增强,这与刺激带宽的异常感知整合相吻合,表明频谱加工改变。频率辨别是声音编码的一个基本方面,对一系列听觉过程,如声源分离和言语理解很重要,因此频率编码中断可能导致FXS和ASD中的一系列听觉问题。在这里,我们使用操作性条件反射音调辨别试验以及听觉皮层和下丘的体内电生理记录,明确表征了雄性Fmr1 KO大鼠的频谱加工缺陷。我们发现Fmr1 KO大鼠表现出较差的频率分辨率,这与听觉皮层神经元的活动亢进和更宽的频率调谐相对应,但在下丘神经元中没有。使用一个基于实验的群体模型,我们表明这些皮层生理差异可以重现观察到的行为辨别缺陷,解码器性能与皮层调谐宽度和信噪比的差异紧密相关。总之,这些发现表明,Fmr1 KO大鼠的皮层兴奋性过高可能以牺牲声音敏感性和精细特征辨别为代价来维持信噪比和信号检测阈值,突出了FXS中一系列听觉行为表型的潜在机制位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceed/12237272/c8ae8602d47b/pbio.3003248.g001.jpg

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