Fregosi Michela, Contestabile Alessandro, Badoud Simon, Borgognon Simon, Cottet Jérôme, Brunet Jean-François, Bloch Jocelyne, Schwab Martin E, Rouiller Eric M
Section of Medicine, Department of Neurosciences and Movement Sciences, Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.
Fribourg Cognition Center, Fribourg, Switzerland.
Front Neuroanat. 2019 May 22;13:50. doi: 10.3389/fnana.2019.00050. eCollection 2019.
The corticotectal projections, together with the corticobulbar (corticoreticular) projections, work in parallel with the corticospinal tract (CST) to influence motoneurons in the spinal cord both directly and indirectly the brainstem descending pathways. The tectospinal tract (TST) originates in the deep layers of the superior colliculus. In the present study, we analyzed the corticotectal projections from two motor cortical areas, namely the premotor cortex (PM) and the primary motor cortex (M1) in eight macaque monkeys subjected to either a cortical lesion of the hand area in M1 ( = 4) or Parkinson's disease-like symptoms PD ( = 4). A subgroup of monkeys with cortical lesion was subjected to anti-Nogo-A antibody treatment whereas all PD monkeys were transplanted with Autologous Neural Cell Ecosystems (ANCEs). The anterograde tracer BDA was used to label the axonal boutons both and in the ipsilateral superior colliculus. Individual axonal boutons were charted in the different layers of the superior colliculus. In intact animals, we previously observed that corticotectal projections were denser when originating from PM than from M1. In the present M1 lesioned monkeys, as compared to intact ones the corticotectal projection originating from PM was decreased when treated with anti-Nogo-A antibody but not in untreated monkeys. In PD-like symptoms' monkeys, on the other hand, there was no consistent change affecting the corticotectal projection as compared to intact monkeys. The present pilot study overall suggests that the corticotectal projection is less affected by M1 lesion or PD symptoms than the corticoreticular projection previously reported in the same animals.
皮质顶盖投射与皮质延髓(皮质网状)投射一起,与皮质脊髓束(CST)并行发挥作用,直接或间接通过脑干下行通路影响脊髓中的运动神经元。顶盖脊髓束(TST)起源于上丘深层。在本研究中,我们分析了八只猕猴中来自两个运动皮层区域,即运动前区(PM)和初级运动皮层(M1)的皮质顶盖投射,这些猕猴分别接受了M1区手部区域的皮质损伤(n = 4)或帕金森病样症状(PD,n = 4)。皮质损伤的猕猴亚组接受了抗Nogo - A抗体治疗,而所有PD猕猴都移植了自体神经细胞生态系统(ANCEs)。顺行示踪剂BDA用于标记同侧上丘中来自PM和M1的轴突终扣。在不同的上丘层中绘制了单个轴突终扣的图谱。在完整动物中,我们之前观察到,源自PM的皮质顶盖投射比源自M1的更密集。在本研究中,与完整猕猴相比,M1损伤的猕猴在接受抗Nogo - A抗体治疗时,源自PM的皮质顶盖投射减少,而未治疗的猕猴则没有。另一方面,与完整猕猴相比,PD样症状的猕猴中,皮质顶盖投射没有一致的变化。本初步研究总体表明,与之前在同一动物中报道的皮质网状投射相比,皮质顶盖投射受M1损伤或PD症状的影响较小。