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Corticotectal Projections From the Premotor or Primary Motor Cortex After Cortical Lesion or Parkinsonian Symptoms in Adult Macaque Monkeys: A Pilot Tracing Study

机译:在成人猕猴的皮质病变或Parkinsonian症状中的皮质或原发性电机皮质的皮质直肠癌突出术:飞行员追查研究

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摘要

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 via 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 (n = 4) or Parkinson’s disease-like symptoms PD (n = 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 en passant and terminaux 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.
机译:的corticotectal突起,与皮质延髓一起(corticoreticular)突起,与所述皮质脊髓束(CST),以在脊髓直接或间接经由脑干下行通路影响运动神经元的并行工作。所述tectospinal道(TST)起源在上丘的深层。在本研究中,我们分析了来自两个电动皮质区域,即前皮层(PM)和经受在M1手区域的任一个皮质病变8只猕猴主运动皮层(M1)的corticotectal突起(N = 4)或帕金森氏病样症状的PD(N = 4)。与皮质损伤猴子一个分组进行抗-Nogo-A抗体治疗,而所有PD猴自体细胞的神经生态系统(ANCEs)移植。顺行示踪剂BDA用于标记的轴突终扣都顺便和terminaux同侧上丘。个别轴突终扣在上丘的不同层绘制。在完整的动物,我们以前观察到corticotectal预测是更密集,当源自PM比M1。在本M1损伤猴,相比于完整的人当与抗-Nogo-A抗体在未处理猴子处理而不是从PM的corticotectal投影始发降低。在PD样症状的猴子,在另一方面,是影响corticotectal投影相比,完整的猴子没有一致的变化。本试验研究总体表明corticotectal投影较少受到M1病变或PD症状比以前在同一个动物报道corticoreticular投影影响。

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