Tactile sensory processing deficits in genetic mouse models of autism spectrum disorder

被引:1
作者
Falcao, Margarida [1 ]
Monteiro, Patricia [1 ]
Jacinto, Luis [1 ]
机构
[1] Fac Med Univ Porto FMUP, Dept Biomed, Expt Biol Unit, P-4200319 Porto, Portugal
关键词
autism spectrum disorder (ASD); mouse models; sensory processing; somatosensory cortex; tactile sensitivity; MICE LACKING; SOMATOSENSORY CORTEX; CEREBRAL-CORTEX; REDUCED EXPRESSION; CANDIDATE GENE; RETT-SYNDROME; PROTEIN; TOUCH; DISRUPTION; CHILDREN;
D O I
10.1111/jnc.16135
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Altered sensory processing is a common feature in autism spectrum disorder (ASD), as recognized in the Diagnostic and Statistical Manual of Mental Disorders (DSM-5). Although altered responses to tactile stimuli are observed in over 60% of individuals with ASD, the neurobiological basis of this phenomenon is poorly understood. ASD has a strong genetic component and genetic mouse models can provide valuable insights into the mechanisms underlying tactile abnormalities in ASD. This review critically addresses recent findings regarding tactile processing deficits found in mouse models of ASD, with a focus on behavioral, anatomical, and functional alterations. Particular attention was given to cellular and circuit-level functional alterations, both in the peripheral and central nervous systems, with the objective of highlighting possible convergence mechanisms across models. By elucidating the impact of mutations in ASD candidate genes on somatosensory circuits and correlating them with behavioral phenotypes, this review significantly advances our understanding of tactile deficits in ASD. Such insights not only broaden our comprehension but also pave the way for future therapeutic interventions.
引用
收藏
页码:2105 / 2123
页数:19
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