• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

自闭症谱系障碍中的感觉异常:聚焦触觉领域,从基因小鼠模型到临床

Sensory Abnormalities in Autism Spectrum Disorders: A Focus on the Tactile Domain, From Genetic Mouse Models to the Clinic.

作者信息

Balasco Luigi, Provenzano Giovanni, Bozzi Yuri

机构信息

Center for Mind/Brain Sciences (CIMeC), University of Trento, Rovereto, Italy.

Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.

出版信息

Front Psychiatry. 2020 Jan 28;10:1016. doi: 10.3389/fpsyt.2019.01016. eCollection 2019.

DOI:10.3389/fpsyt.2019.01016
PMID:32047448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6997554/
Abstract

Sensory abnormalities are commonly recognized as diagnostic criteria in autism spectrum disorder (ASD), as reported in the last edition of the Diagnostic and Statistical Manual of Mental Disorder (DSM-V). About 90% of ASD individuals have atypical sensory experiences, described as both hyper- and hypo-reactivity, with abnormal responses to tactile stimulation representing a very frequent finding. In this review, we will address the neurobiological bases of sensory processing in ASD, with a specific focus of tactile sensitivity. In the first part, we will review the most relevant sensory abnormalities detected in ASD, and then focus on tactile processing deficits through the discussion of recent clinical and experimental studies. In the search for the neurobiological bases of ASD, several mouse models have been generated with knockout and humanized knockin mutations in many ASD-associated genes. Here, we will therefore give a brief overview of the anatomical structure of the mouse somatosensory system, and describe the somatosensory abnormalities so far reported in different mouse models of ASD. Understanding the neurobiological bases of sensory processing in ASD mouse models may represent an opportunity for a better comprehension of the mechanisms underlying sensory abnormalities, and for the development of novel effective therapeutic strategies.

摘要

如最新版《精神疾病诊断与统计手册》(DSM - V)所报道,感觉异常通常被视为自闭症谱系障碍(ASD)的诊断标准。约90%的ASD个体有非典型的感觉体验,表现为过度敏感和反应不足,对触觉刺激的异常反应是非常常见的发现。在本综述中,我们将探讨ASD中感觉处理的神经生物学基础,特别关注触觉敏感性。在第一部分,我们将回顾在ASD中检测到的最相关的感觉异常,然后通过讨论最近的临床和实验研究,聚焦于触觉处理缺陷。在寻找ASD的神经生物学基础过程中,已经产生了几种在许多与ASD相关基因中具有敲除和人源化敲入突变的小鼠模型。因此,在这里我们将简要概述小鼠体感系统的解剖结构,并描述迄今为止在不同ASD小鼠模型中报道的体感异常。了解ASD小鼠模型中感觉处理的神经生物学基础可能为更好地理解感觉异常背后的机制以及开发新的有效治疗策略提供契机。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/266a/6997554/a3eafd463654/fpsyt-10-01016-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/266a/6997554/72e26e294570/fpsyt-10-01016-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/266a/6997554/a3eafd463654/fpsyt-10-01016-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/266a/6997554/72e26e294570/fpsyt-10-01016-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/266a/6997554/a3eafd463654/fpsyt-10-01016-g002.jpg

相似文献

1
Sensory Abnormalities in Autism Spectrum Disorders: A Focus on the Tactile Domain, From Genetic Mouse Models to the Clinic.自闭症谱系障碍中的感觉异常:聚焦触觉领域,从基因小鼠模型到临床
Front Psychiatry. 2020 Jan 28;10:1016. doi: 10.3389/fpsyt.2019.01016. eCollection 2019.
2
Tactile sensory processing deficits in genetic mouse models of autism spectrum disorder.自闭症谱系障碍遗传小鼠模型的触觉感觉处理缺陷。
J Neurochem. 2024 Sep;168(9):2105-2123. doi: 10.1111/jnc.16135. Epub 2024 Jun 4.
3
Gene Expression Profiling in Trigeminal Ganglia from Cntnap2 and Shank3b Mouse Models of Autism Spectrum Disorder.自闭症谱系障碍Cntnap2 和 Shank3b 小鼠模型三叉神经节中的基因表达谱分析。
Neuroscience. 2023 Nov 1;531:75-85. doi: 10.1016/j.neuroscience.2023.08.028. Epub 2023 Sep 10.
4
Cortex-restricted deletion of Foxp1 impairs barrel formation and induces aberrant tactile responses in a mouse model of autism.Cortex-restricted deletion of Foxp1 impairs barrel formation and induces aberrant tactile responses in a mouse model of autism. 皮层特异性 Foxp1 缺失破坏了自闭症小鼠模型中桶状皮层的形成并导致异常触觉反应。
Mol Autism. 2023 Sep 11;14(1):34. doi: 10.1186/s13229-023-00567-0.
5
Autism spectrum disorder in the scope of tactile processing.自闭症谱系障碍的触觉加工范围。
Dev Cogn Neurosci. 2018 Jan;29:140-150. doi: 10.1016/j.dcn.2016.12.005. Epub 2016 Dec 23.
6
Normal Evoked Response to Rapid Sequences of Tactile Pulses in Autism Spectrum Disorders.自闭症谱系障碍中对快速触觉脉冲序列的正常诱发反应。
Front Hum Neurosci. 2016 Sep 16;10:433. doi: 10.3389/fnhum.2016.00433. eCollection 2016.
7
Somatosensory Temporal Discrimination in Autism Spectrum Disorder.自闭症谱系障碍中的体感时间辨别。
Autism Res. 2021 Apr;14(4):656-667. doi: 10.1002/aur.2479. Epub 2021 Feb 1.
8
Touch and olfaction/taste differentiate children carrying a 16p11.2 deletion from children with ASD.触觉和嗅觉/味觉可区分携带 16p11.2 缺失的儿童和 ASD 儿童。
Mol Autism. 2021 Feb 5;12(1):8. doi: 10.1186/s13229-020-00410-w.
9
Targeting Peripheral Somatosensory Neurons to Improve Tactile-Related Phenotypes in ASD Models.靶向周围感觉神经元改善 ASD 模型的触觉相关表型。
Cell. 2019 Aug 8;178(4):867-886.e24. doi: 10.1016/j.cell.2019.07.024.
10
Impaired tactile processing in children with autism spectrum disorder.自闭症谱系障碍儿童触觉加工受损。
J Neurophysiol. 2014 May;111(9):1803-11. doi: 10.1152/jn.00890.2013. Epub 2014 Feb 12.

引用本文的文献

1
Neuroplasticity-Based Approaches to Sensory Processing Alterations in Autism Spectrum Disorder.基于神经可塑性的方法治疗自闭症谱系障碍中的感觉处理改变
Int J Mol Sci. 2025 Jul 23;26(15):7102. doi: 10.3390/ijms26157102.
2
Sensory processing, emotional and behavioural challenges in children with autism spectrum disorder and attention deficit hyperactive disorder.自闭症谱系障碍和注意力缺陷多动障碍儿童的感觉处理、情绪及行为挑战
Int J Dev Disabil. 2023 Dec 18;71(5):703-713. doi: 10.1080/20473869.2023.2277601. eCollection 2025.
3
PTEN in somatostatin neurons regulates fear and anxiety and is required for inhibitory synaptic connectivity within central amygdala.

本文引用的文献

1
Whisker Nuisance Test: A Valuable Tool to Assess Tactile Hypersensitivity in Mice.触须干扰测试:评估小鼠触觉超敏反应的重要工具。
Bio Protoc. 2019 Aug 20;9(16):e3331. doi: 10.21769/BioProtoc.3331.
2
Targeting Peripheral Somatosensory Neurons to Improve Tactile-Related Phenotypes in ASD Models.靶向周围感觉神经元改善 ASD 模型的触觉相关表型。
Cell. 2019 Aug 8;178(4):867-886.e24. doi: 10.1016/j.cell.2019.07.024.
3
Maternal Immune Activation during Pregnancy Alters the Behavior Profile of Female Offspring of Sprague Dawley Rats.
生长抑素神经元中的PTEN调节恐惧和焦虑,并且是中央杏仁核内抑制性突触连接所必需的。
Front Cell Neurosci. 2025 Jun 26;19:1597131. doi: 10.3389/fncel.2025.1597131. eCollection 2025.
4
NEXMIF overexpression is associated with autism-like behaviors and alterations in dendritic arborization and spine formation in mice.NEXMIF过表达与小鼠的自闭症样行为以及树突分支和棘突形成的改变有关。
Front Neurosci. 2025 Jun 18;19:1556570. doi: 10.3389/fnins.2025.1556570. eCollection 2025.
5
The endocannabinoidome-gut microbiome-brain axis as a novel therapeutic target for autism spectrum disorder.内源性大麻素系统-肠道微生物群-脑轴作为自闭症谱系障碍的新型治疗靶点。
J Biomed Sci. 2025 Jul 2;32(1):60. doi: 10.1186/s12929-025-01145-7.
6
A randomized controlled trial into the effectiveness of a mobile health application (SAM) to reduce stress and improve well-being in autistic adults.一项关于移动健康应用程序(SAM)在减轻自闭症成年人压力和改善其幸福感方面有效性的随机对照试验。
Autism. 2025 Jun 26;29(10):13623613251346885. doi: 10.1177/13623613251346885.
7
Management of critical care emergencies in children with autism spectrum disorder.自闭症谱系障碍儿童危重症紧急情况的管理
World J Crit Care Med. 2025 Jun 9;14(2):99975. doi: 10.5492/wjccm.v14.i2.99975.
8
Shared Immune and Nutrient Metabolism Pathways Between Autism Spectrum Disorder and Celiac Disease: An In Silico Approach.自闭症谱系障碍与乳糜泻之间共享的免疫和营养代谢途径:一种计算机模拟方法。
Nutrients. 2025 Apr 25;17(9):1439. doi: 10.3390/nu17091439.
9
mutation manifests in abnormal gastrointestinal morphology and function in mice.突变在小鼠的胃肠道形态和功能异常中表现出来。
Front Neurosci. 2025 Apr 17;19:1552369. doi: 10.3389/fnins.2025.1552369. eCollection 2025.
10
Comparison of abnormal sensory symptoms in children with and without autism spectrum disorder.患有和未患自闭症谱系障碍的儿童异常感觉症状的比较。
Pak J Med Sci. 2025 Apr;41(4):1181-1186. doi: 10.12669/pjms.41.4.11486.
孕期母体免疫激活改变了 Sprague Dawley 大鼠雌性后代的行为特征。
eNeuro. 2019 Apr 19;6(2). doi: 10.1523/ENEURO.0437-18.2019. eCollection 2019 Mar-Apr.
4
Retinal defects in mice lacking the autism-associated gene Engrailed-2.缺失自闭症相关基因 Engrailed-2 的小鼠的视网膜缺陷。
Neuroscience. 2019 Jun 1;408:177-190. doi: 10.1016/j.neuroscience.2019.03.061. Epub 2019 Apr 10.
5
Selection bias on intellectual ability in autism research: a cross-sectional review and meta-analysis.自闭症研究中的智力能力选择偏差:横断面研究和荟萃分析。
Mol Autism. 2019 Mar 1;10:9. doi: 10.1186/s13229-019-0260-x. eCollection 2019.
6
Aberrant Somatosensory Processing and Connectivity in Mice Lacking .缺乏. 的小鼠异常的躯体感觉处理和连接
J Neurosci. 2019 Feb 20;39(8):1525-1538. doi: 10.1523/JNEUROSCI.0612-18.2018. Epub 2018 Dec 28.
7
Are Children Severely Affected by Autism Spectrum Disorder Underrepresented in Treatment Studies? An Analysis of the Literature.自闭症谱系障碍儿童在治疗研究中是否代表性不足?文献分析。
J Autism Dev Disord. 2019 Apr;49(4):1378-1390. doi: 10.1007/s10803-018-3844-y.
8
SYNGAP1 heterozygosity disrupts sensory processing by reducing touch-related activity within somatosensory cortex circuits.SYNGAP1 杂合性通过减少躯体感觉皮层回路中与触摸相关的活动来破坏感觉处理。
Nat Neurosci. 2018 Dec;21(12):1-13. doi: 10.1038/s41593-018-0268-0. Epub 2018 Nov 21.
9
Impaired perceptual learning in a mouse model of Fragile X syndrome is mediated by parvalbumin neuron dysfunction and is reversible.脆性 X 综合征小鼠模型中感觉学习受损是由颗粒蛋白神经元功能障碍介导的,且是可逆转的。
Nat Neurosci. 2018 Oct;21(10):1404-1411. doi: 10.1038/s41593-018-0231-0. Epub 2018 Sep 24.
10
Neural Circuit Mechanisms of Social Behavior.社会行为的神经回路机制。
Neuron. 2018 Apr 4;98(1):16-30. doi: 10.1016/j.neuron.2018.02.026.