首页> 外文期刊>Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism >Longitudinal monitoring of mesoscopic cortical activity in a mouse model of microinfarcts reveals dissociations with behavioral and motor function
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Longitudinal monitoring of mesoscopic cortical activity in a mouse model of microinfarcts reveals dissociations with behavioral and motor function

机译:微小鼠模型中的介观皮质活性的纵向监测微遗传学的模型揭示了与行为和运动功能的解剖

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Small vessel disease is characterized by sporadic obstruction of small vessels leading to neuronal cell death. These microinfarcts often escape detection by conventional magnetic resonance imaging and are identified only upon postmortem examination. Our work explores a brain-wide microinfarct model in awake head-fixed mice, where occlusions of small penetrating arterioles are reproduced by endovascular injection of fluorescent microspheres. Mesoscopic functional connectivity was mapped longitudinally in awake GCaMP6 mice using genetically encoded calcium indicators for transcranial wide-field calcium imaging. Microsphere occlusions were quantified and changes in cerebral blood flow were measured with laser speckle imaging. The neurodeficit score in microinfarct mice was significantly higher than in sham, indicating impairment in motor function. The novel object recognition test showed a reduction in the discrimination index in microinfarct mice compared to sham. Graph-theoretic analysis of functional connectivity did not reveal significant differences in functional connectivity between sham and microinfarct mice. While behavioral tasks revealed impairments following microinfarct induction, the absence of measurable functional alterations in cortical activity has a less straightforward interpretation. The behavioral alterations produced by this model are consistent with alterations observed in human patients suffering from microinfarcts and support the validity of microsphere injection as a microinfarct model.
机译:小血管疾病的特点是散发梗阻导致神经元细胞死亡。这些MicroInFarcts经常通过常规磁共振成像逃逸检测,并且仅在后期检查时鉴定。我们的作品探讨了唤醒头固定小鼠中的脑宽的微临时模型,其中小穿透动脉瘤的闭塞通过血管内注射荧光微球再现。使用遗传编码的经颅宽场钙成像钙指示剂在清醒GCAMP6小鼠中纵向映射介相函数连通性。用激光散斑成像量化微球诱发,并测量脑血流的变化。微梗死小鼠的神经缺点得分明显高于假,表明电机功能的损伤。新的对象识别试验表明,与假的微量遗物小鼠中的鉴别指数降低。功能连通性的图形理论分析没有揭示假和微量梗死小鼠之间的功能连通性的显着差异。虽然行为任务揭示了微量遗传诱导后的损伤,但皮质活动中没有可测量的功能改变具有不太直接的解释。该模型产生的行为改变与人类患者患有患有MicroInFarcts的患者的改变一致,并支持微球注射作为MicroInfarct模型的有效性。

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