Early movement restriction impairs the development of sensorimotor integration, motor skills and memory in rats: Towards a preclinical model of developmental coordination disorder?

IF 2.7 4区 医学 Q3 NEUROSCIENCES European Journal of Neuroscience Pub Date : 2024-11-10 DOI:10.1111/ejn.16594
Hanane Khalki, Diego Cabral Lacerda, Corane Karoutchi, Maxime Delcour, Orlane Dupuis, Marine Kochmann, Jean-Michel Brezun, Erwan Dupont, Mamta Amin, Muriel Darnaudéry, Marie-Hélène Canu, Mary F Barbe, Jacques-Olivier Coq
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Abstract

Children with neurodevelopmental disorders, such as developmental coordination disorder (DCD), exhibit gross to fine sensorimotor impairments, reduced physical activity and interactions with the environment and people. This disorder co-exists with cognitive deficits, executive dysfunctions and learning impairments. Previously, we demonstrated in rats that limited amounts and atypical patterns of movements and somatosensory feedback during early movement restriction manifested in adulthood as degraded postural and locomotor abilities, and musculoskeletal histopathology, including muscle atrophy, hyperexcitability within sensorimotor circuitry and maladaptive cortical plasticity, leading to functional disorganization of the primary somatosensory and motor cortices in the absence of cortical histopathology. In this study, we asked how this developmental sensorimotor restriction (SMR) started to impact the integration of multisensory information and the emergence of sensorimotor reflexes in rats. We also questioned the enduring impact of SMR on motor activities, pain and memory. SMR led to deficits in the emergence of swimming and sensorimotor reflexes, the development of pain and altered locomotor patterns and posture with toe-walking, adult motor performance and night spontaneous activity. In addition, SMR induced exploratory hyperactivity, short-term impairments in object-recognition tasks and long-term deficits in object-location tasks. SMR rats displayed minor alterations in histological features of the hippocampus, entorhinal, perirhinal and postrhinal cortices yet no obvious changes in the prefrontal cortex. Taken all together, these results show similarities with the symptoms observed in children with DCD, although further exploration seems required to postulate whether developmental SMR corresponds to a rat model of DCD.

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早期运动限制会损害大鼠的感觉运动整合、运动技能和记忆的发育:建立发育协调障碍的临床前模型?
患有发育协调障碍(DCD)等神经发育障碍的儿童表现出粗大到精细的感知运动障碍、体力活动减少以及与环境和人的互动减少。这种障碍与认知缺陷、执行功能障碍和学习障碍同时存在。此前,我们曾在大鼠身上证实,在早期运动受限期间,有限的运动量和不典型的运动模式以及躯体感觉反馈在成年后表现为姿势和运动能力的退化以及肌肉骨骼组织病理学,包括肌肉萎缩、感觉运动回路内的过度兴奋性和不适应性皮质可塑性,从而导致初级躯体感觉和运动皮质在没有皮质组织病理学的情况下出现功能紊乱。在这项研究中,我们询问这种发育过程中的感觉运动限制(SMR)如何开始影响大鼠多感觉信息的整合以及感觉运动反射的出现。我们还询问了感知运动限制对运动活动、疼痛和记忆的持久影响。SMR导致游泳和感觉运动反射的出现出现缺陷、疼痛的发展以及运动模式和脚趾行走姿势的改变、成年运动表现和夜间自发活动。此外,SMR 会诱发探索性多动、物体识别任务的短期障碍和物体定位任务的长期障碍。SMR大鼠的海马、内视网膜、周围和后视网膜皮层的组织学特征有轻微改变,但前额叶皮层没有明显变化。综上所述,这些结果显示出与在患有精神发育障碍的儿童身上观察到的症状的相似性,但要推测发育性SMR是否与精神发育障碍的大鼠模型相对应,似乎还需要进一步的探索。
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来源期刊
European Journal of Neuroscience
European Journal of Neuroscience 医学-神经科学
CiteScore
7.10
自引率
5.90%
发文量
305
审稿时长
3.5 months
期刊介绍: EJN is the journal of FENS and supports the international neuroscientific community by publishing original high quality research articles and reviews in all fields of neuroscience. In addition, to engage with issues that are of interest to the science community, we also publish Editorials, Meetings Reports and Neuro-Opinions on topics that are of current interest in the fields of neuroscience research and training in science. We have recently established a series of ‘Profiles of Women in Neuroscience’. Our goal is to provide a vehicle for publications that further the understanding of the structure and function of the nervous system in both health and disease and to provide a vehicle to engage the neuroscience community. As the official journal of FENS, profits from the journal are re-invested in the neuroscientific community through the activities of FENS.
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