首页> 外文期刊>The Journal of Comparative Neurology >Direct projections of omnipause neurons to reticulospinal neurons: a double-labeling light microscopic study in the cat.
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Direct projections of omnipause neurons to reticulospinal neurons: a double-labeling light microscopic study in the cat.

机译:OmnipAuse神经元直接投影到网状神经元:猫的双标记光显微镜研究。

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摘要

Omnipause neurons (OPNs) are inhibitory neurons located in the midline region of the caudal pons. Their role in gating the discharges of saccade-related burst neurons is well known, but there is no agreement concerning their influence on brainstem neurons that control other muscle groups participating in rapid gaze shifts. In the present study, we inquired whether OPNs project directly to pontobulbar reticulospinal neurons (RSNs) in the cat. Retrograde transport of horseradish peroxidase from the cervical spinal cord was used to label RSNs and an anterograde tracer (biocytin) was iontophoresed at sites of extracellular recording of the OPN activity. Somadendritic characteristics of biocytin-labeled OPNs were largely similar to those obtained previously with intracellular labeling. Three-dimensional reconstruction of axonal trajectories and collaterals revealed that projections of OPNs, regarded as a population, are bilateral. Their terminals were restricted to the reticular formation and midline structures throughout the rostral bulbar and pontine tegmentum. Appositions of synaptic boutons originating from five fully stained OPNs were detected on 38 retrogradely labeled RSNs, each of the OPNs contacting 3-13 cells. The numbers of boutons (1-46; mean 11.8) on the RSN somata and proximal dendrites indicate that the anatomical strength of paired OPN-RSN connections is comparable to that of other similarly studied inhibitory neurons in the cat. The existence of connections with RSNs supports the hypothesis of a generalized influence of OPNs on several effectors participating in orienting gaze shifts as opposed to the idea of their strict specialization for the control of eye saccades.
机译:OmnipAuse Neurons(OPN)是位于尾部中线区域的抑制神经元。他们在众所周知的扫描相关爆发神经元的放电方面的作用,但没有关于它们对控制参与快速凝视变化的其他肌肉团体的脑干神经元的影响。在本研究中,我们询问opns是否直接向猫的Pontobulbar括号(RSNS)进行。将辣根过氧化物酶从颈脊髓逆行传递用于标记RSNS,并且在OPN活性的细胞外记录部位进行蒽曲面示踪剂(生物霉素)。生物霉素标记的OPN的小胺特征在很大程度上与先前用细胞内标记得到的那些。轴突轨迹和抵押品的三维重建透露,OPN的投影被视为人口,是双边的。它们的终端仅限于整个鼻孔泡和猪Tegmentum的网状形成和中线结构。在逆行标记的RSNS上检测到源自五种完全染色OPN的突触突出子,每种OPN接触3-13细胞。 RSN Somata和近端树突上的Boutons(1-46;平均11.8)的数量表明配对OPN-RSN连接的解剖强度与猫中的其他类似研究的抑制神经元的解剖学强度相当。与RSN的存在支持OPN对参与定向凝视变化的几个效果的广义影响的假设,而不是对其对眼扫描控制的严格专业化的想法。

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