Hackett J T, Buchheim A
J Comp Neurol. 1984 Apr 10;224(3):425-36. doi: 10.1002/cne.902240310.
The output connections of the cranial relay neurons, part of the Mauthner cell network, were examined in goldfish with light and electron microscopic techniques. Either lucifer yellow or horseradish peroxidase (HRP) was injected into cranial relay neuron axons to demonstrate that they diverge to several motor nuclei and to many motoneurons within one nucleus. Retrograde transport of the enzyme from injections of mandibular muscles was used to label the trigeminal motoneurons. In the electron microscope, cranial relay neuron processes were distinguished by the granular appearance of the electron-opaque polymer formed enzymatically by HRP, while the retrogradely labeled motoneurons had the polymer enclosed in lysosomes. The cranial relay neuron terminals contained many presynaptic vesicles which concentrated the HRP reaction product. Active zones and synaptic clefts were evident. At some synapses, both gap junctions and presynaptic vesicles were found. The mechanism of synaptic transmission was investigated by simultaneous recording with two intracellular microelectrodes from cranial relay neuron-motoneuron pairs. Composite postsynaptic potentials in a trigeminal motoneuron were evoked by intracellular stimulation of a cranial relay neuron axon. The earliest excitatory postsynaptic potential (EPSP) component had a latency of 0.25 msec and had a peak amplitude that was not depressed by repetitive stimulation. A second component had larger peak amplitudes which were reduced easily by repetitive stimulation. Antidromic action potentials were not transmitted from motoneurons to the cranial relay neuron axons. Thus, both electrical and chemical transmission probably occur at the cranial relay neuron-motoneuron synapses. Since the cranial relay neurons fire synchronously and receive excitatory chemical synapses, the function of the gap junctions and electrical transmission is unclear. Perhaps the importance of these gap junctions is more for transport of small molecules than for impulse transmission.
运用光学和电子显微镜技术,对金鱼体内作为Mauthner细胞网络一部分的脑中继神经元的输出连接进行了研究。将荧光素黄或辣根过氧化物酶(HRP)注入脑中继神经元轴突,以证明它们会发散至多个运动核以及一个核内的许多运动神经元。通过将酶从下颌肌肉注射处逆行运输来标记三叉神经运动神经元。在电子显微镜下,脑中继神经元的突起可通过HRP酶促形成的电子不透明聚合物的颗粒状外观来区分,而逆行标记的运动神经元则有包裹在溶酶体中的聚合物。脑中继神经元终末含有许多突触前囊泡,这些囊泡聚集了HRP反应产物。活性区和突触间隙清晰可见。在一些突触处,同时发现了缝隙连接和突触前囊泡。通过用两个细胞内微电极同时记录脑中继神经元 - 运动神经元对,研究了突触传递机制。通过对脑中继神经元轴突进行细胞内刺激,可诱发三叉神经运动神经元中的复合突触后电位。最早的兴奋性突触后电位(EPSP)成分潜伏期为0.25毫秒,其峰值幅度不会因重复刺激而降低。第二个成分的峰值幅度更大,容易因重复刺激而减小。逆向动作电位不会从运动神经元传递至脑中继神经元轴突。因此,电传递和化学传递可能都发生在脑中继神经元 - 运动神经元突触处。由于脑中继神经元同步放电并接受兴奋性化学突触,缝隙连接和电传递的功能尚不清楚。或许这些缝隙连接的重要性更多在于小分子的运输而非冲动传递。