Chan Hugh H, Cooperrider Jessica L, Park Hyun-Joo, Wathen Connor A, Gale John T, Baker Kenneth B, Machado Andre G
Department of Neurosciences, Lerner Research Institute, Cleveland Clinic Cleveland, OH, USA.
Department of Neurosciences, Lerner Research Institute, Cleveland ClinicCleveland, OH, USA; Center for Neurological Restoration, Cleveland ClinicCleveland, OH, USA.
Front Aging Neurosci. 2017 Feb 17;9:10. doi: 10.3389/fnagi.2017.00010. eCollection 2017.
Crossed cerebellar diaschisis (CCD) is a functional deficit of the cerebellar hemisphere resulting from loss of afferent input consequent to a lesion of the contralateral cerebral hemisphere. It is manifested as a reduction of metabolism and blood flow and, depending on severity and duration, it can result in atrophy, a phenomenon known as crossed cerebellar atrophy (CCA). While CCA has been well-demonstrated in humans, it remains poorly characterized in animal models of stroke. In this study we evaluated the effects of cerebral cortical ischemia on contralateral cerebellar anatomy using an established rodent model of chronic stroke. The effects of cortical ischemia on the cerebellar hemispheres, vermis and deep nuclei were characterized. Intracortical microinjections of endothelin-1 (ET-1) were delivered to the motor cortex of Long Evans rats to induce ischemic stroke, with animals sacrificed 6 weeks later. Naive animals served as controls. Cerebral sections and cerebellar sections including the deep nuclei were prepared for analysis with Nissl staining. Cortical ischemia was associated with significant thickness reduction of the molecular layer at the Crus 1 and parafloccular lobule (PFL), but not in fourth cerebellar lobule (4Cb), as compared to the ipsilesional cerebellar hemisphere. A significant reduction in volume and cell density of the lateral cerebellar nucleus (LCN), the rodent correlate of the dentate nucleus, was also noted. The results highlight the relevance of corticopontocerebellar (CPC) projections for cerebellar metabolism and function, including its direct projections to the LCN.
交叉性小脑失联络(CCD)是由于对侧大脑半球病变导致传入输入丧失而引起的小脑半球功能缺陷。它表现为代谢和血流减少,根据严重程度和持续时间的不同,可导致萎缩,即交叉性小脑萎缩(CCA)现象。虽然CCA在人类中已得到充分证实,但在中风动物模型中其特征仍不明确。在本研究中,我们使用已建立的慢性中风啮齿动物模型评估了大脑皮质缺血对侧小脑解剖结构的影响。对皮质缺血对小脑半球、蚓部和深部核团的影响进行了特征描述。向Long Evans大鼠的运动皮质内微量注射内皮素-1(ET-1)以诱导缺血性中风,6周后处死动物。未经处理的动物作为对照。制备包括深部核团在内的大脑切片和小脑切片,用尼氏染色进行分析。与同侧小脑半球相比,皮质缺血与 Crus 1和旁绒球小叶(PFL)分子层厚度显著降低有关,但在第四小脑小叶(4Cb)则不然。还观察到外侧小脑核(LCN,相当于啮齿动物的齿状核)体积和细胞密度显著降低。结果突出了皮质-脑桥-小脑(CPC)投射对小脑代谢和功能的相关性,包括其对LCN的直接投射。