Graduate Neuroscience Program, University of California, Riverside, USA.
Department of Otolaryngology-Head and Neck Surgery, Medical University of South Carolina, Charleston, USA.
J Neurodev Disord. 2024 May 8;16(1):24. doi: 10.1186/s11689-024-09539-8.
Autism spectrum disorder (ASD) is currently diagnosed in approximately 1 in 44 children in the United States, based on a wide array of symptoms, including sensory dysfunction and abnormal language development. Boys are diagnosed ~ 3.8 times more frequently than girls. Auditory temporal processing is crucial for speech recognition and language development. Abnormal development of temporal processing may account for ASD language impairments. Sex differences in the development of temporal processing may underlie the differences in language outcomes in male and female children with ASD. To understand mechanisms of potential sex differences in temporal processing requires a preclinical model. However, there are no studies that have addressed sex differences in temporal processing across development in any animal model of ASD.
To fill this major gap, we compared the development of auditory temporal processing in male and female wildtype (WT) and Fmr1 knock-out (KO) mice, a model of Fragile X Syndrome (FXS), a leading genetic cause of ASD-associated behaviors. Using epidural screw electrodes, we recorded auditory event related potentials (ERP) and auditory temporal processing with a gap-in-noise auditory steady state response (ASSR) paradigm at young (postnatal (p)21 and p30) and adult (p60) ages from both auditory and frontal cortices of awake, freely moving mice.
The results show that ERP amplitudes were enhanced in both sexes of Fmr1 KO mice across development compared to WT counterparts, with greater enhancement in adult female than adult male KO mice. Gap-ASSR deficits were seen in the frontal, but not auditory, cortex in early development (p21) in female KO mice. Unlike male KO mice, female KO mice show WT-like temporal processing at p30. There were no temporal processing deficits in the adult mice of both sexes.
These results show a sex difference in the developmental trajectories of temporal processing and hypersensitive responses in Fmr1 KO mice. Male KO mice show slower maturation of temporal processing than females. Female KO mice show stronger hypersensitive responses than males later in development. The differences in maturation rates of temporal processing and hypersensitive responses during various critical periods of development may lead to sex differences in language function, arousal and anxiety in FXS.
根据广泛的症状,包括感觉功能障碍和语言发育异常,目前美国大约每 44 名儿童中就有 1 名被诊断为自闭症谱系障碍 (ASD)。男孩的诊断率比女孩高约 3.8 倍。听觉时间处理对于语音识别和语言发展至关重要。时间处理的异常发育可能是 ASD 语言障碍的原因。男性和女性 ASD 儿童的语言结果差异可能源于时间处理发育方面的性别差异。要了解时间处理方面潜在性别差异的机制,需要一个临床前模型。然而,目前尚无研究在任何 ASD 动物模型中探讨时间处理在整个发育过程中的性别差异。
为了填补这一重大空白,我们比较了雄性和雌性野生型 (WT) 和 Fmr1 敲除 (KO) 小鼠(脆性 X 综合征 (FXS) 的模型,FXS 是一种导致 ASD 相关行为的主要遗传原因)听觉时间处理的发育情况。使用硬膜外螺丝电极,我们在清醒、自由活动的小鼠的听觉和额皮质中,使用噪声中的间隙听觉稳态反应 (ASSR) 范式,记录听觉事件相关电位 (ERP) 和听觉时间处理,记录时间从幼年期(出生后 (p)21 和 p30)到成年期(p60)。
结果表明,与 WT 对照相比,Fmr1 KO 小鼠在整个发育期的 ERP 幅度均增强,成年雌性 KO 小鼠的增强幅度大于成年雄性 KO 小鼠。在雌性 KO 小鼠的早期发育(p21),仅在前额皮质而非听觉皮质中出现了间隙 ASSR 缺陷。与雄性 KO 小鼠不同,雌性 KO 小鼠在 p30 时表现出与 WT 相似的时间处理能力。成年雄性和雌性 KO 小鼠均无时间处理缺陷。
这些结果表明,Fmr1 KO 小鼠的时间处理和超敏反应的发育轨迹存在性别差异。雄性 KO 小鼠的时间处理成熟速度比雌性慢。在发育后期,雌性 KO 小鼠的超敏反应强于雄性。在各种关键发育时期,时间处理和超敏反应的成熟速度差异可能导致 FXS 中语言功能、觉醒和焦虑方面的性别差异。