Bio-Imaging Lab, Department of Biomedical Sciences, University of Antwerp, Wilrijk, 2610, Belgium.
Bio-Imaging Lab, Department of Biomedical Sciences, University of Antwerp, Wilrijk, 2610, Belgium; Centre of Biosciences, Institute of Animal Biochemistry and Genetics, Slovak Academy of Sciences, Bratislava, Slovakia.
Neuroimage. 2018 Nov 1;181:190-202. doi: 10.1016/j.neuroimage.2018.07.010. Epub 2018 Jul 5.
Similar to human speech, bird song is controlled by several pathways including a cortico-basal ganglia-thalamo-cortical (C-BG-T-C) loop. Neurotoxic disengagement of the basal ganglia component, i.e. Area X, induces long-term changes in song performance, while most of the lesioned area regenerates within the first months. Importantly however, the timing and spatial extent of structural neuroplastic events potentially affecting other constituents of the C-BG-T-C loop is not clear. We designed a longitudinal MRI study where changes in brain structure were evaluated relative to the time after neurotoxic lesioning or to vocal performance. By acquiring both Diffusion Tensor Imaging and 3-dimensional anatomical scans, we were able to track alterations in respectively intrinsic tissue properties and local volume. Voxel-based statistical analyses revealed structural remodeling remote to the lesion, i.e. in the thalamus and, surprisingly, the cerebellum, both peaking within the first two months after lesioning Area X. Voxel-wise correlations between song performance and MRI parameters uncovered intriguing brain-behavior relationships in several brain areas pertaining to the C-BG-T-C loop supervising vocal motor control. Our results clearly point to structural neuroplasticity in the cerebellum induced by basal ganglia (striatal) damage and might point to the existence of a human-like cerebello-thalamic-basal ganglia pathway capable of modifying vocal motor output.
类似于人类的言语,鸟类的鸣唱也受到几个通路的控制,包括皮质基底神经节-丘脑-皮质(C-BG-T-C)回路。基底神经节成分(即 X 区)的神经毒性分离会导致鸣唱表现的长期变化,而大部分受损区域在头几个月内会再生。然而,重要的是,潜在影响 C-BG-T-C 回路其他成分的结构神经可塑性事件的时间和空间范围尚不清楚。我们设计了一项纵向 MRI 研究,其中评估了相对于神经毒性损伤后时间或发声表现的脑结构变化。通过获取弥散张量成像和三维解剖扫描,我们能够分别追踪内在组织特性和局部体积的变化。基于体素的统计分析显示,损伤后的大脑结构重塑发生在远离损伤部位的区域,即丘脑,以及令人惊讶的是,小脑,这两种情况都在 X 区损伤后两个月内达到峰值。歌声表现与 MRI 参数之间的体素相关性揭示了与 C-BG-T-C 回路有关的几个大脑区域的有趣的脑-行为关系,这些区域监管着发声运动控制。我们的结果清楚地表明,基底神经节(纹状体)损伤会导致小脑的结构神经可塑性,这可能表明存在类似于人类的小脑-丘脑-基底神经节通路,能够修饰发声运动输出。