社会环境对野生型和自闭症小鼠模型嗅觉和社交能力的影响

IF 5.8 1区 医学 Q1 PSYCHIATRY
Caroline Gora, Ana Dudas, Lucas Court, Anil Annamneedi, Gaëlle Lefort, Thiago S Nakahara, Nicolas Azzopardi, Adrien Acquistapace, Anne-Lyse Laine, Anne-Charlotte Trouillet, Lucile Drobecq, Emmanuel Pecnard, Benoît Piégu, Pascale Crépieux, Pablo Chamero, Lucie P Pellissier
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引用次数: 0

摘要

自闭症谱系障碍(ASD)是一种复杂、多基因和异质性的神经发育疾病。自闭症相关变异的严重程度受环境因素的影响,尤其是神经发育关键时期的社会经历。虽然早期行为干预对一些自闭症儿童有疗效,但目前还缺乏针对核心特征(社会交往和沟通障碍以及刻板或限制性行为)的药物支持。在这项研究中,我们考察了社会环境如何影响野生型(WT)小鼠和 Shank3 基因敲除(KO)小鼠(一种反映类似自闭症核心特征的模型)。我们的研究结果表明,慢性社会隔离增强了 WT 动物的社会互动和嗅觉神经元反应。此外,它还能恢复 Shank3 KO 小鼠在社会新奇偏好和嗅觉功能以及自我梳理方面的损伤。相反,在丰富的社会环境中,WT 小鼠对新的同种动物的社会兴趣增强了,但在 Shank3 KO 小鼠中却产生了相反的效果。值得注意的是,Shank3 KO小鼠在与WT或Shank3 KO小鼠接触时会表现出不同的社会反应。这些结果提供了新的见解,有助于对患有自闭症的儿童实施行为干预和包容性课堂计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of the social environment on olfaction and social skills in wild-type and a mouse model of autism.

Autism spectrum disorders (ASD) are complex, polygenic and heterogenous neurodevelopmental conditions. The severity of autism-associated variants is influenced by environmental factors, particularly social experiences during the critical neurodevelopmental period. While early behavioral interventions have shown efficacy in some children with autism, pharmacological support for core features - impairments in social interaction and communication, and stereotyped or restricted behaviors - is currently lacking. In this study, we examined how the social environment influences both wild-type (WT) and Shank3 knockout (KO) mice, a model reflecting core autism-like traits. Our findings revealed that chronic social isolation enhanced social interaction and olfactory neuron responses in WT animals. Furthermore, it restored impairments in social novelty preference and olfactory function, as well as self-grooming in Shank3 KO mice. Conversely, an enriched social environment heightened social interest toward novel conspecifics in WT mice, but elicited the opposite effect in Shank3 KO mice. Notably, Shank3 KO mice displayed distinct social responses when exposed to WT or Shank3 KO mice. These results offer novel insights that could favor the implementation of behavioral interventions and inclusive classroom programs for children with ASD.

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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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