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首页> 外文期刊>Neurochemistry International: The International Journal for the Rapid Publication of Critical Reviews, Preliminary and Original Research Communications in Neurochemistry >Correlative study using structural MRI and super-resolution microscopy to detect structural alterations induced by long-term optogenetic stimulation of striatal medium spiny neurons
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Correlative study using structural MRI and super-resolution microscopy to detect structural alterations induced by long-term optogenetic stimulation of striatal medium spiny neurons

机译:使用结构MRI和超分辨率显微镜检测纹状体培养型刺刺激性神经元长期致敏刺激诱导的结构改变的相关性研究

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摘要

Striatal medium spiny neurons (MSNs) control motor function. Hyper- or hypo-activity of MSNs coincides with basal ganglia-related movement disorders. Based on the assumption that lasting alterations in neuronal activity lead to structural changes in the brain, understanding these structural alterations may be used to infer MSN functional abnormalities. To infer MSN function from structural data, understanding how long-lasting alterations in MSN activity affect brain morphology is essential. To address this, we utilized a simplified model of functional induction by stimulating MSNs expressing channelrhodopsin 2 (ChR2). Subsequent structural alterations which induced long-term activity changes in these MSNs were investigated in the striatal pathway and its associated regions by diffusion tensor imaging (DTI) and histological assessment with super-resolution microscopy. DTI detected changes in the striatum, substantia nigra, and motor cortex. Histological assessment found a reduction in the diameter of myelinated cortical axons as well as MSN dendrites and axons. The structural changes showed a high correlation between DTI parameters and histological data. These results demonstrated that long-term neural activation in the MSNs alters the diameter of MSN and cortical neurons fibers. This study provides a tool for understanding the causal relationship between functional and structural alterations.
机译:薄层培养基刺神经元(MSNS)控制电机功能。 MSNS的超级或Hypo-Activity与基础神经节相关的运动障碍。基于假设神经元活动持续改变导致大脑结构变化,理解这些结构改变可用于推断MSN功能异常。从结构数据推断MSN功能,了解MSN活性的持久改变如何影响脑形态是必不可少的。为了解决这一点,我们利用了通过刺激表达频道的MSNS表示患者的模型2(CHR2)来使用简化的功能诱导模型。通过扩散张量成像(DTI)和具有超分辨率显微镜的组织学评估,在纹状体途径及其相关区域中研究了这些MSN中这些MSN的长期活性变化的后续结构改变。 DTI检测到纹状体,体积NIGRA和电机皮层的变化。组织学评估发现骨髓皮质轴突的直径降低以及MSN树枝状和轴突。结构变化显示了DTI参数和组织学数据之间的高相关性。这些结果表明,MSN中的长期神经激活改变了MSN和皮质神经元纤维的直径。本研究提供了一种理解功能性和结构改变之间的因果关系的工具。

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