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猫脊髓运动神经元上反复抑制性突触的空间分布。

Spatial distribution of recurrent inhibitory synapses on spinal motoneurons in the cat.

作者信息

Fyffe R E

机构信息

Department of Physiology, University of North Carolina, Chapel Hill 27599-7545.

出版信息

J Neurophysiol. 1991 May;65(5):1134-49. doi: 10.1152/jn.1991.65.5.1134.

Abstract
  1. Intracellular staining of Renshaw cells and alpha motoneurons was used to determine the spatial distribution of recurrent inhibitory synapses on spinal motoneurons in the cat. In each experiment, a Renshaw cell and one or more possible target motoneurons were labeled with horseradish peroxidase after physiological identification. 2. Paris of labeled neurons were reconstructed and measured at the light microscopic level. As defined by light microscopy, presumed synaptic contacts between nine Renshaw cells and 10 postsynaptic motoneurons were observed. On average, each Renshaw cell made three synaptic contacts (range 1-9) on each motoneuron. 3. Electron microscopic confirmation of several presumed contacts provided evidence that the appositions identified by light microscopic criteria are genuine contacts between Renshaw cell boutons and the labeled motoneuron. 4. All of the identified synapses observed in these experiments were located on motoneuron dendrites, between 65 and 706 microns from the soma. Use of a simplified cable model indicated that the synapses are electrotonically close to the soma, the average location being approximately 0.25 length constants from the soma (range 0.04-0.82 lambda). 5. These observations provide direct evidence to support the hypothesis that Renshaw cell synapses on motoneurons are located on the dendrites and not on the cell body (whereas reciprocal inhibitory synapses, from Ia inhibitory interneurons, are predominantly located on the soma). The functional significance of the observed distribution of Renshaw inhibitory synapses is discussed. One possibility is that the recurrent inhibitory pathway selectively inhibits particular dendritic inputs.
摘要
  1. 采用对闰绍细胞和α运动神经元进行细胞内染色的方法,来确定猫脊髓运动神经元上回返性抑制性突触的空间分布。在每个实验中,经生理学鉴定后,用辣根过氧化物酶标记一个闰绍细胞和一个或多个可能的靶运动神经元。2. 在光学显微镜水平对标记的神经元对进行重建和测量。根据光学显微镜的定义,观察到9个闰绍细胞与10个突触后运动神经元之间存在假定的突触联系。平均而言,每个闰绍细胞在每个运动神经元上形成3个突触联系(范围为1 - 9个)。3. 对几个假定联系的电子显微镜证实提供了证据,表明根据光学显微镜标准鉴定的并置结构是闰绍细胞终扣与标记的运动神经元之间的真实联系。4. 在这些实验中观察到的所有已鉴定突触均位于运动神经元树突上,距胞体65至706微米。使用简化的电缆模型表明,这些突触在电紧张性上靠近胞体,平均位置距胞体约0.25个长度常数(范围为0.04 - 0.82λ)。5. 这些观察结果提供了直接证据,支持以下假说:闰绍细胞在运动神经元上的突触位于树突而不是细胞体上(而来自Ia抑制性中间神经元的交互抑制性突触主要位于细胞体上)。文中讨论了所观察到的闰绍抑制性突触分布的功能意义。一种可能性是,回返性抑制通路选择性地抑制特定的树突输入。

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