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产前缺血后成年大鼠脑白质损伤的神经解剖、感觉运动和认知缺陷。

Neuroanatomical, sensorimotor and cognitive deficits in adult rats with white matter injury following prenatal ischemia.

机构信息

UMR 6149 Neurobiologie Intégrative et Adaptative, CNRS-Aix-Marseille Université, Marseille.

出版信息

Brain Pathol. 2012 Jan;22(1):1-16. doi: 10.1111/j.1750-3639.2011.00504.x. Epub 2011 Aug 16.

DOI:10.1111/j.1750-3639.2011.00504.x
PMID:21615591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8028965/
Abstract

Perinatal brain injury including white matter damage (WMD) is highly related to sensory, motor or cognitive impairments in humans born prematurely. Our aim was to examine the neuroanatomical, functional and behavioral changes in adult rats that experienced prenatal ischemia (PI), thereby inducing WMD. PI was induced by unilateral uterine artery ligation at E17 in pregnant rats. We assessed performances in gait, cognitive abilities and topographical organization of maps, and neuronal and glial density in primary motor and somatosensory cortices, the hippocampus and prefrontal cortex, as well as axonal degeneration and astrogliosis in white matter tracts. We found WMD in corpus callosum and brainstem, and associated with the hippocampus and somatosensory cortex, but not the motor cortex after PI. PI rats exhibited mild locomotor impairments associated with minor signs of spasticity. Motor map organization and neuronal density were normal in PI rats, contrasting with major somatosensory map disorganization, reduced neuronal density, and a marked reduction of inhibitory interneurons. PI rats exhibited spontaneous hyperactivity in open-field test and short-term memory deficits associated with abnormal neuronal density in related brain areas. Thus, this model reproduces in adult PI rats the main deficits observed in infants with a perinatal history of hypoxia-ischemia and WMD.

摘要

围产期脑损伤包括白质损伤(WMD)与早产儿的感觉、运动或认知障碍高度相关。我们的目的是研究经历产前缺血(PI)从而导致 WMD 的成年大鼠的神经解剖、功能和行为变化。PI 通过在怀孕大鼠的 E17 时单侧子宫动脉结扎来诱导。我们评估了步态、认知能力和地形图组织、初级运动和体感皮质、海马体和前额叶皮质中的神经元和神经胶质密度,以及白质束中的轴突变性和星形胶质增生。我们发现,PI 后在胼胝体和脑干中出现 WMD,并与海马体和体感皮质相关,而与运动皮质无关。PI 大鼠表现出轻度运动障碍,伴有轻微的痉挛迹象。PI 大鼠的运动图组织和神经元密度正常,但体感图严重紊乱,神经元密度降低,抑制性中间神经元明显减少。PI 大鼠在旷场试验中表现出自发性过度活跃,短期记忆缺陷与相关脑区异常神经元密度有关。因此,该模型在成年 PI 大鼠中重现了具有围产期缺氧缺血和 WMD 病史的婴儿中观察到的主要缺陷。

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