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Diverse action of repeated corticosterone treatment on synaptic transmission neuronal plasticity and morphology in superficial and deep layers of the rat motor cortex

机译:反复皮质酮治疗对大鼠运动皮层浅层和深层突触传递神经元可塑性和形态的多种作用

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摘要

One of the adverse effects of prolonged stress in rats is impaired performance of skilled reaching and walking tasks. The mechanisms that lead to these abnormalities are incompletely understood. Therefore, we compared the effects of twice daily repeated corticosterone injections for 7 days on miniature excitatory postsynaptic currents (mEPSCs), as well as on synaptic plasticity and morphology of layers II/III and V pyramidal neurons of the primary motor cortex (M1) of male Wistar rats. Corticosterone treatment resulted in increased frequency, but not amplitude, of mEPSCs in layer II/III neurons accompanied by increased complexity of the apical part of their dendritic tree, with no changes in the density of dendritic spines. The frequency and amplitude of mEPSCs as well as the parameters characterizing the complexity of the dendritic tree were not changed in layer V cells; however, their dendritic spine density was increased. While corticosterone treatment resulted in an increase in the amplitude of field potentials evoked in intralaminar connections within layer II/III, it did not influence field responses in layer V intralaminar connections, as well as the extent of chemically induced layer V long-term potentiation (chemLTP) by the application of tetraethylammonium (TEA, 25 mM). However, chemLTP induction in layer II/III was impaired in slices prepared from corticosterone-treated animals. These data indicate that repeated 7-day administration of exogenous corticosterone induces structural and functional plasticity in the M1, which occurs mainly in layer II/III pyramidal neurons. These findings shed light on potential sites of action and mechanisms underlying stress-induced impairment of motor functions.
机译:长时间应力对大鼠的不利影响之一是熟练的伸手和步行任务的表现受损。导致这些异常的机制尚不完全清楚。因此,我们比较了连续7天每天两次注射皮质酮对微型兴奋性突触后电流(mEPSC)以及对主运动皮层(M1)的II / III和V层锥体神经元的突触可塑性和形态的影响。雄性Wistar大鼠。皮质酮治疗导致II / III层神经元中mEPSC的频率增加,但幅度没有增加,同时其树突状树的根尖部分的复杂性增加,而树突棘的密度没有变化。在V层细胞中,mEPSC的频率和幅度以及表征树枝状树的复杂性的参数没有改变。然而,它们的树突棘密度增加了。尽管皮质酮治疗导致II / III层内层内连接诱发的场电位振幅增加,但它并未影响V层内层连接的场响应以及化学诱导的V层长期增强的程度( chemLTP)通过应用四乙铵(TEA,25mM)。但是,在由皮质酮处理的动物制备的切片中,II / III层的chemLTP诱导作用减弱。这些数据表明,重复施用7天的外源性皮质酮可诱导M1中的结构和功能可塑性,这种可塑性主要发生在II / III层锥体神经元中。这些发现揭示了潜在的作用部位和潜在的压力诱导的运动功能受损的机制。

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