Spinocerebellar neurons projecting to copula pyramidis, studied by retrograde labeling in the rat.

IF 2.7 3区 医学 Q1 ANATOMY & MORPHOLOGY
Matsuo Matsushita
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引用次数: 0

Abstract

Spinal neurons project to the vermis and the intermediate part of the hemisphere of the anterior lobe. In the posterior lobe, neurons projecting to the intermediate part, the copular part (copula pyramidis) of the paramedian lobule, differ from those projecting to the vermis in the cat. The present study by the retrograde labeling reveals that the projection patterns in copula pyramidis in the rat are similar to those identified in the cat. The projections through uncrossed ascending axons originate from (1) neurons in the medial part of laminae V and VI of the C2-T1 segments, (2) neurons in lamina V of the C7-L3 segments, (3) the marginal neurons of Clarke's column, and (4) neurons of Clarke's column of the lower thoracic and the lumbar segments. The projections through crossed ascending axons originate from (5) the lateral group of the ventral spinocerebellar tract neurons in the T12-L3 segments, (6) Stilling's sacral nuclei, and (7) the central cervical nucleus. The present findings suggest that the spinal inputs from the specific neuronal groups define the functions of copula pyramidis.

大鼠脊髓小脑神经元向锥体突起的逆行标记研究。
脊髓神经元投射到蚓部和前叶半球的中间部分。在后叶,神经元投射到中间部分,即旁小叶的锥体部分(锥体锥体),与猫的蚓部不同。本研究通过逆行标记揭示了大鼠copula锥体的投影模式与猫相似。通过未交叉上行轴突的投射来自(1)C2-T1节段V和VI板内侧的神经元,(2)C7-L3节段V板的神经元,(3)Clarke’s柱边缘的神经元,(4)下胸段和腰椎节段Clarke’s柱的神经元。通过交叉上行轴突的投射来自(5)T12-L3节段脊髓小脑束腹侧组神经元,(6)stillling骶核,(7)颈中央核。目前的研究结果表明,来自特定神经元群的脊髓输入决定了锥体的功能。
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来源期刊
Brain Structure & Function
Brain Structure & Function 医学-解剖学与形态学
CiteScore
6.00
自引率
6.50%
发文量
168
审稿时长
8 months
期刊介绍: Brain Structure & Function publishes research that provides insight into brain structure−function relationships. Studies published here integrate data spanning from molecular, cellular, developmental, and systems architecture to the neuroanatomy of behavior and cognitive functions. Manuscripts with focus on the spinal cord or the peripheral nervous system are not accepted for publication. Manuscripts with focus on diseases, animal models of diseases, or disease-related mechanisms are only considered for publication, if the findings provide novel insight into the organization and mechanisms of normal brain structure and function.
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