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从七鳃鳗后脑网状后核到参与七鳃鳗运动控制的脊髓神经元的单突触兴奋性氨基酸传递。

Monosynaptic excitatory amino acid transmission from the posterior rhombencephalic reticular nucleus to spinal neurons involved in the control of locomotion in lamprey.

作者信息

Ohta Y, Grillner S

机构信息

Nobel Institute for Neurophysiology, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Neurophysiol. 1989 Nov;62(5):1079-89. doi: 10.1152/jn.1989.62.5.1079.

Abstract
  1. The reticulospinal neurons in the lamprey posterior rhombencephalic reticular nucleus (PRRN) and their projections to different types of spinal neurons have been investigated by the use of simultaneous paired intracellular recordings from one pre- and one postsynaptic cell. PRRN is of particular importance for the initiation of locomotion. 2. Intracellular stimulation of single PRRN neurons produced monosynaptic excitatory postsynaptic potentials (EPSPs) in simultaneously recorded motoneurons and spinal premotor interneurons of both the excitatory and inhibitory type. Individual PRRN neurons produced EPSPs in several different types of target cells, as revealed by signal averaging. Each single PRRN neuron had extensive monosynaptic connections to approximately 73% of the motoneuronal population. Conversely, several PRRN neurons converge on individual spinal neurons. The average amplitude of the EPSPs was 0.43 +/- 0.40 (SD) mV. The EPSPs varied in time course (time to peak = 7.5 +/- 2.8 ms; duration at one-half peak amplitude = 21.9 +/- 18.1 ms). 3. The EPSPs produced by reticulospinal cells were composed of either exclusively chemical, exclusively electrical, or mixed chemical and electrical components. The electrical EPSPs remained when the ordinary physiological solution was substituted for one without Ca2+ but with Mn2+. The chemical component of the EPSPs was always depressed when a broad-spectrum excitatory amino acid (EAA) antagonist, such as kynurenic acid, was applied, suggesting that the chemical component was because of EAA transmission. The chemical EPSP could have two components, one late, suppressed by N-methyl-D-aspartate (NMDA) antagonists, and one early because of activation of kainate/quisqualate receptors. 4. Three-dimensional reconstructions of Lucifer yellow-filled PRRN neurons were performed with a confocal laser scanning microscope. PRRN neurons producing monosynaptic excitatory amino acid EPSPs were found to have a fusiform cell body located near the surface of the fourth ventricle and an extensive fanlike dendritic tree extending to the ventral and lateral margin of the brain stem within the basal plate. The axons descend in the lateral funiculi of the spinal cord. 5. PRRN neurons utilizing EAA transmission are active during fictive locomotion. They presumably initiate and reinforce ongoing spinal locomotor activity by monosynaptically increasing the general excitability of the spinal premotor interneurons of the spinal locomotor networks by means of their extensive divergent and convergent monosynaptic connections.
摘要
  1. 利用对一个突触前细胞和一个突触后细胞同时进行配对细胞内记录的方法,对七鳃鳗后脑后部网状核(PRRN)中的网状脊髓神经元及其向不同类型脊髓神经元的投射进行了研究。PRRN对于运动的启动尤为重要。2. 对单个PRRN神经元进行细胞内刺激,在同时记录的运动神经元以及兴奋性和抑制性类型的脊髓前运动中间神经元中产生了单突触兴奋性突触后电位(EPSP)。信号平均显示,单个PRRN神经元在几种不同类型的靶细胞中产生EPSP。每个单个PRRN神经元与约73%的运动神经元群体有广泛的单突触连接。相反,几个PRRN神经元会聚于单个脊髓神经元。EPSP的平均幅度为0.43±0.40(标准差)mV。EPSP在时间进程上有所不同(峰值时间 = 7.5±2.8毫秒;半峰幅度持续时间 = 21.9±18.1毫秒)。3. 网状脊髓细胞产生的EPSP由纯化学性、纯电性或化学性与电性混合的成分组成。当用不含Ca2+但含Mn2+的溶液替代普通生理溶液时,电性EPSP依然存在。当应用广谱兴奋性氨基酸(EAA)拮抗剂(如犬尿氨酸)时,EPSP的化学成分总是受到抑制,这表明化学成分是由于EAA传递所致。化学性EPSP可能有两个成分,一个较晚出现,可被N - 甲基 - D - 天冬氨酸(NMDA)拮抗剂抑制,另一个较早出现,是由于海人藻酸/quisqualate受体的激活。4. 使用共聚焦激光扫描显微镜对用荧光黄填充的PRRN神经元进行了三维重建。发现产生单突触兴奋性氨基酸EPSP的PRRN神经元具有梭形细胞体,位于第四脑室表面附近,并有一个广泛的扇形树突伸向基板内脑干的腹侧和外侧边缘。轴突沿脊髓外侧索下行。5. 利用EAA传递信号的PRRN神经元在虚拟运动期间活跃。它们大概通过广泛的发散和会聚单突触连接,单突触地增加脊髓运动网络中脊髓前运动中间神经元的总体兴奋性,从而启动并加强正在进行的脊髓运动活动。

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