Premotor Cortical-Cerebellar Reorganization in a Macaque Model of Primary Motor Cortical Lesion and Recovery

被引:20
作者
Yamamoto, Tatsuya [1 ,2 ]
Hayashi, Takuya [3 ]
Murata, Yumi [2 ]
Ose, Takayuki [3 ]
Higo, Noriyuki [2 ]
机构
[1] Tsukuba Int Univ, Fac Med & Hlth Sci, Tsuchiura, Ibaraki 3000051, Japan
[2] Natl Inst Adv Ind Sci & Technol, Human Informat Res Inst, Tsukuba, Ibaraki 3058568, Japan
[3] RIKEN, Ctr Biosyst Dynam Res, Lab Brain Connect Imaging, Kobe, Hyogo 6500047, Japan
关键词
biotin dextran amine; cerebellar compartmentalization; fastigial nucleus; monkey; neural circuits; plasticity; FUNCTIONAL-ORGANIZATION; MANUAL DEXTERITY; CORTEX LESION; POSTNATAL-DEVELOPMENT; SENSORIMOTOR CORTEX; SPINAL-CORD; ALDOLASE-C; PROJECTIONS; MONKEY; TRACT;
D O I
10.1523/JNEUROSCI.0077-19.2019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuromotor systems have the capacity for functional recovery following local damage. The literature suggests a possible role for the premotor cortex and cerebellum in motor recovery. However, the specific changes to interactions between these areas following damage remain unclear. Here, we demonstrate potential rewiring of connections from the ipsilesional ventral premotor cortex (ip-PMv) to cerebellar structures in a nonhuman primate model of primary motor cortex (M1) lesion and motor recovery. Cerebellar connections arising from the ip-PMv were investigated by comparing biotinylated dextran amine (BDA) between two groups of male Macaca mulatta: M1-lesion/motor recovery group and intact group. There were more BDA-labeled boutons and axons in all ipsilesional deep cerebellar nuclei (fastigial, interposed, and dentate) in the M1-lesion/recovery group than in the intact group. The difference was evident in the ipsilesional fastigial nucleus (ip-FN), and particularly observed in its middle, a putative somatosensory region of the ip-FN, which was characterized by absent or little expression of aldolase C. Some of the altered projections from the ip-PMv to ip-FN neurons were confirmed as functional because the synaptic markers, synaptophysin and vesicular glutamate transporter 1, were colocalized with BDA-labeled boutons. These results suggest that the adult primate brain after motor lesions can reorganize large-scale networks to enable motor recovery by enhancing sensorimotor coupling and motor commands via rewired fronto-cerebellar connections.
引用
收藏
页码:8484 / 8496
页数:13
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