谷氨酸的
神经科学
多巴胺能
基底神经节
足前核
帕金森病
多巴胺
神经退行性变
加巴能
间接运动途径
直接运动途径
生物
帕金森病
纹状体
谷氨酸受体
脑深部刺激
中枢神经系统
医学
疾病
抑制性突触后电位
内科学
生物化学
受体
作者
Débora Masini,Ole Kiehn
标识
DOI:10.1038/s41467-022-28075-4
摘要
Abstract The pedunculopontine nucleus (PPN) is a locomotor command area containing glutamatergic neurons that control locomotor initiation and maintenance. These motor actions are deficient in Parkinson’s disease (PD), where dopaminergic neurodegeneration alters basal ganglia activity. Being downstream of the basal ganglia, the PPN may be a suitable target for ameliorating parkinsonian motor symptoms. Here, we use in vivo cell-type specific PPN activation to restore motor function in two mouse models of parkinsonism made by acute pharmacological blockage of dopamine transmission. With a combination of chemo- and opto-genetics, we show that excitation of caudal glutamatergic PPN neurons can normalize the otherwise severe locomotor deficit in PD, whereas targeting the local GABAergic population only leads to recovery of slow locomotion. The motor rescue driven by glutamatergic PPN activation is independent of activity in nearby locomotor promoting glutamatergic Cuneiform neurons. Our observations point to caudal glutamatergic PPN neurons as a potential target for neuromodulatory restoration of locomotor function in PD.
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