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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 >MRI heralds secondary nigral lesion after brain ischemia in mice: a secondary time window for neuroprotection
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MRI heralds secondary nigral lesion after brain ischemia in mice: a secondary time window for neuroprotection

机译:MRI预示小鼠脑缺血后继发性黑色病变:神经保护的继发时间窗

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摘要

Cerebral ischemia in the territory of the middle cerebral artery (MCA) can induce delayed neuronal cell death in the ipsilateral substantia nigra (SN) remote from the primary ischemic lesion. This exofocal postischemic neuronal degeneration (EPND) may worsen stroke outcomes. However, the mechanisms leading to EPND are poorly understood. Here, we studied the time course of EPND via sequential magnetic resonance imaging (MRI) and immunohistochemistry for up to 28 days after 30 minutes occlusion of the MCA (MCAo) and reperfusion in the mouse. Furthermore, the effects of delayed treatment with FK506 and MK-801 on the development of EPND were investigated. Secondary neuronal degeneration in the SN occurred within the first week after MCAo and was characterized by a marked neuronal cell loss on histology. Sequential neuroimaging examinations revealed transient MRI changes, which were detectable as early as day 4 after MCAo and thus heralding histologic evidence of EPND. Treatment with MK-801, an established anti-excitotoxic agent, conferred protection against EPND even when initiated days after the initial ischemic event, which was not evident with FK506. Our findings define a secondary time window for delayed neuroprotection after stroke, which may provide a promising target for the development of novel therapies.
机译:大脑中动脉(MCA)区域的脑缺血可诱导远离原发性缺血病变的同侧黑质(SN)延迟神经元细胞死亡。这种带外缺血后神经元变性(EPND)可能会使卒中预后恶化。但是,导致EPND的机制了解甚少。在这里,我们通过闭塞MCA(MCAo)和小鼠再灌注30分钟后,通过顺序磁共振成像(MRI)和免疫组织化学研究了EPND的时程长达28天。此外,研究了用FK506和MK-801延迟治疗对EPND发生的影响。 SN中继发性神经元变性发生在MCAo后的第一周,其特征是组织学上明显的神经元细胞丢失。连续的神经影像学检查显示出短暂的MRI变化,最早在MCAo后第4天就可以检测到,因此预示着EPND的组织学证据。使用MK-801(一种既定的抗兴奋剂)进行治疗,即使在初始缺血事件发生数日后开始使用,也可以保护EPND,这在FK506中并不明显。我们的发现确定了卒中后延迟神经保护的次要时间窗,这可能为开发新疗法提供有希望的目标。

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