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中缝背核神经元之间的染料偶联

Dye coupling between dorsal raphe neurones.

作者信息

Stezhka V V, Lovick T A

机构信息

Department of Physiology, Medical School, Birmingham, UK.

出版信息

Exp Brain Res. 1995;105(3):383-90. doi: 10.1007/BF00233038.

DOI:10.1007/BF00233038
PMID:7498392
Abstract

Neurones in the dorsal raphe nucleus (DRN) were impaled and filled with biocytin in coronal slices of midbrain taken from young adult rats. The electrophysiological properties and gross morphology of the cells were similar to those reported previously for serotonergic neurones in the DRN. Of 27 cases in which filled neurones were recovered in histological material, almost half (48%) showed labelling of two or three cells, although only one cell had been recorded from. Coupled cells were identified as close or distantly coupled, depending on the distance from the soma of the presumed impaled cell (23.5 +/- 15 microns, n = 7 and 150 +/- 26.5 microns, n = 10 respectively). Whereas close-coupled cells may have been artefactually "coupled" by the penetrating electrode, coupling between distant cells is most likely to be a result of transfer of biocytin through gap junctions. Camera lucida reconstructions of pairs of labelled cells revealed extensive overlap of dendritic fields and numerous crossings between dendrites. When examined at high magnification under a light microscope, many of the crossing dendrites were found to travel in different focal planes. Nevertheless, for each pair of cells, at least one point of close apposition was observed between dendrites or between the axon and a dendrite of the presumed impaled and coupled cell. The incidence of dye coupling between neurones in the DRN may reflect a relatively high level of electronic coupling between the neurones. This form of coupling may be important in determining the synchronous nature of firing of neurones in the DRN.

摘要

在取自年轻成年大鼠的中脑冠状切片中,对背侧中缝核(DRN)中的神经元进行刺入并注入生物胞素。这些细胞的电生理特性和大体形态与先前报道的DRN中5-羟色胺能神经元的特性和形态相似。在27例组织学材料中回收了注入生物胞素的神经元,其中近一半(48%)显示有两三个细胞被标记,尽管记录的仅一个细胞。根据与假定刺入细胞的胞体的距离,耦合细胞被确定为紧密耦合或远距离耦合(分别为23.5±15微米,n = 7和150±26.5微米,n = 10)。紧密耦合的细胞可能是被刺入电极人为地“耦合”,而远距离细胞之间的耦合很可能是生物胞素通过缝隙连接转移的结果。对成对标记细胞的明场重建显示树突野广泛重叠,树突之间有许多交叉。在光学显微镜下高倍观察时,发现许多交叉的树突在不同的焦平面中穿行。然而,对于每对细胞,在假定的刺入和耦合细胞的树突之间或轴突与树突之间至少观察到一个紧密并置点。DRN中神经元之间染料耦合的发生率可能反映了神经元之间相对较高水平的电耦合。这种耦合形式对于确定DRN中神经元放电的同步性质可能很重要。

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