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海月水母的中枢神经回路。II:环状巨神经元和载体系统。

Central circuitry in the jellyfish Aglantha. II: The ring giant and carrier systems.

作者信息

Mackie G, Meech R

出版信息

J Exp Biol. 1995;198(Pt 11):2271-8. doi: 10.1242/jeb.198.11.2271.

DOI:10.1242/jeb.198.11.2271
PMID:9320190
Abstract
  1. The ring giant axon in the outer nerve ring of the jellyfish Aglantha digitale is a multinucleate syncytium 85 % of which is occupied by an electron-dense fluid-filled vacuole apparently in a Gibbs­Donnan equilibrium with the surrounding band of cytoplasmic cortex. Micropipette recordings show small (-15 to -25 mV) and large (-62 to -66 mV) resting potentials. Low values, obtained with a high proportion of the micropipette penetrations, are assumed to be from the central vacuole; high values from the cytoplasmic cortex. Background electrical activity includes rhythmic oscillations and synaptic potentials representing hair cell input caused by vibration. 2. After the ring giant axon has been cut, propagating action potentials evoked by stimulation are conducted past the cut and re-enter the axon on the far side. The system responsible (the carrier system) through-conducts at a velocity approximately 25 % of that of the ring giant axon and is probably composed of small neurones running in parallel with it. Numerous small neurones are seen by electron microscopy, some making one-way and some two-way synapses with the ring giant. 3. Despite their different conduction velocities, the two systems normally appear to fire in synchrony and at the velocity of the ring giant axon. We suggest that, once initiated, ring giant spikes propagate rapidly around the margin, firing the carrier neurones through serial synapses and giving them, in effect, the same high conduction velocity. Initiation of ring giant spikes can, however, require input from the carrier system. The spikes are frequently seen to be mounted on slow positive potentials representing summed carrier postsynaptic potentials. 4. The carrier system fires one-for-one with the giant axons of the tentacles and may mediate impulse traffic between the latter and the ring giant axon. We suggest that the carrier system may also provide the pathways from the ring giant to the motor giant axons used in escape swimming. 5. The findings show that the ring giant axon functions in close collaboration with the carrier system, increasing the latter's effective conduction velocity, and that interactions with other neuronal sub-systems are probably mediated exclusively by the carrier system.
摘要
  1. 太平洋僧帽水母外部神经环中的环状巨轴突是一种多核合胞体,其中85%被电子致密的充满液体的液泡占据,该液泡显然与周围的细胞质皮质带处于吉布斯-唐南平衡状态。微电极记录显示出小的(-15至-25毫伏)和大的(-62至-66毫伏)静息电位。在高比例的微电极穿刺中获得的低值被认为来自中央液泡;高值来自细胞质皮质。背景电活动包括节律性振荡和代表由振动引起的毛细胞输入的突触电位。2. 在环状巨轴突被切断后,由刺激诱发的传播动作电位传导经过切口并在远侧重新进入轴突。负责的系统(载体系统)以大约环状巨轴突速度25%的速度进行通透传导,并且可能由与其平行运行的小神经元组成。通过电子显微镜可以看到许多小神经元,其中一些与环状巨轴突形成单向突触,一些形成双向突触。3. 尽管它们的传导速度不同,但这两个系统通常似乎同步放电,且放电速度与环状巨轴突的速度相同。我们认为,一旦启动,环状巨轴突尖峰就会迅速在边缘传播,通过串联突触激发载体神经元,并实际上赋予它们相同的高传导速度。然而,环状巨轴突尖峰的启动可能需要来自载体系统的输入。这些尖峰经常被看到叠加在代表载体突触后电位总和的缓慢正电位上。4. 载体系统与触手的巨轴突一对一放电,并且可能介导后者与环状巨轴突之间的冲动传递。我们认为,载体系统也可能提供从环状巨轴突到用于逃避游泳的运动巨轴突的通路。5. 这些发现表明,环状巨轴突与载体系统密切协作发挥作用,提高了后者的有效传导速度,并且与其他神经元子系统的相互作用可能仅由载体系统介导。

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