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本文引用的文献

1
Pharmacology and Nerve-endings (Walter Ernest Dixon Memorial Lecture): (Section of Therapeutics and Pharmacology).药理学与神经末梢(沃尔特·欧内斯特·迪克森纪念讲座):(治疗学与药理学分会)
Proc R Soc Med. 1935 Jan;28(3):319-32. doi: 10.1177/003591573502800330.
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Electrical Interaction of Paired Ganglion Cells in the Leech.对盲鳗成对神经节细胞的电相互作用研究。
J Gen Physiol. 1963 Jan 1;46(3):573-87. doi: 10.1085/jgp.46.3.573.
3
Aspects of the organization of central nervous pathways in Aplysia depilans.海兔中枢神经通路的组织学方面
J Exp Biol. 1962 Mar;39:45-69. doi: 10.1242/jeb.39.1.45.
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ELECTROPHYSIOLOGY OF THE FETAL SPINAL CORD. I. ACTION POTENTIALS OF THE MOTONEURON.胎儿脊髓的电生理学。I. 运动神经元的动作电位
J Gen Physiol. 1964 May;47(5):1003-22. doi: 10.1085/jgp.47.5.1003.
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AN ELECTROPHYSIOLOGICAL STUDY OF THE ANATOMICAL RELATIONS OF TWO GIANT NERVE CELLS IN APLYSIA DEPILANS.光滑滨螺中两个巨型神经细胞解剖学关系的电生理学研究
J Exp Biol. 1963 Sep;40:469-86. doi: 10.1242/jeb.40.3.469.
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Intracellular and extracellular responses of the several regions of the Mauthner cell of the goldfish.金鱼Mauthner细胞几个区域的细胞内和细胞外反应。
J Neurophysiol. 1962 Nov;25:732-71. doi: 10.1152/jn.1962.25.6.732.
7
Cholinergic transmission mechanisms for both excitation and inhibition in molluscan central synapses.软体动物中枢突触中兴奋和抑制的胆碱能传递机制。
Nature. 1961 Oct 28;192:366-7. doi: 10.1038/192366a0.
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A cholinergic mechanism of inhibitory synaptic transmission in a molluscan nervous system.软体动物神经系统中抑制性突触传递的胆碱能机制。
J Neurophysiol. 1962 Mar;25:236-62. doi: 10.1152/jn.1962.25.2.236.
9
The path of the giant cell axons in Aplysia depilans.海兔巨细胞轴突的路径。
Nature. 1961 Jul 22;191:404-5. doi: 10.1038/191404a0.
10
Synaptic inhibition in giant nerve cell of Onchidium verruculatum.疣背石磺巨大神经细胞中的突触抑制
J Neurophysiol. 1961 Mar;24:167-75. doi: 10.1152/jn.1961.24.2.167.

海兔左右巨细胞之间的直接突触连接。

A direct synaptic connexion between the left and right giant cells in Aplysia.

作者信息

Hughes G M, Tauc L

出版信息

J Physiol. 1968 Aug;197(3):511-27. doi: 10.1113/jphysiol.1968.sp008572.

DOI:10.1113/jphysiol.1968.sp008572
PMID:4299013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1351746/
Abstract
  1. In Aplysia fasciata, intrasomatic stimulation of the giant cell (RGC) of the right upper quadrant of the abdominal ganglia is followed after a constant delay by the appearance of a synaptic potential recorded in the giant cell (LGC) of the left pleural ganglion.2. The synaptic potential recorded in the LGC soma has a biphasic form (hence biphasic post-synaptic potential or BPSP) consisting of a fast depolarizing phase of about 200-800 muV amplitude and 0.15-0.25 sec duration, followed by a slow hyperpolarizing phase of about 200-800 muV amplitude and 1-3 sec duration.3. During repetitive stimulation summation results in an over-all hyperpolarization at low frequencies (less than 5/sec) and an over-all depolarization for higher frequencies. Very high frequencies (25/sec) of stimulation of the RGC may elicit a spike in the LGC.4. Stimulation with two shocks showed increasing effects with shorter intervals on both the depolarizing and hyperpolarizing phase. These effects were progressive and there was no falling out of one of the two phases as might be expected if the BPSP was a composite of an inhibitory post-synaptic potential (IPSP) and an excitatory post-synaptic potential (EPSP).5. The effects of artificially imposed polarization of the LGC through a second micro-electrode suggest that the BPSP results from a chemical transmission mechanism for both its depolarizing and hyperpolarizing phases but electrical transmission cannot be excluded.6. Curare has no effect on the BPSP and thus excludes a cholinergic transmission mechanism. Chloride ions injected into the LGC soma do not appear to modify the BPSP and hence it is concluded that the hyperpolarizing phase is different from IPSPs of the same cell.7. No synaptic potential is recorded in the RGC following stimulation of the LGC, except in a single preparation in which the RGC soma was situated in the right pleural ganglion. In this case the synaptic potential recorded in both giant cells following stimulation of the other, was biphasic in form.8. It is concluded that the BPSP is a unitary monosynaptic potential which is a characteristic feature of the organization of these two giant cells.
摘要
  1. 在 Fasciata 海兔中,对腹神经节右上象限的巨细胞(RGC)进行胞内刺激后,经过一段恒定延迟,左侧胸膜神经节的巨细胞(LGC)中会记录到一个突触电位。

  2. 在 LGC 胞体中记录到的突触电位呈双相形式(因此称为双相突触后电位或 BPSP),由一个快速去极化相和一个缓慢超极化相组成。快速去极化相的幅度约为 200 - 800 μV,持续时间为 0.15 - 0.25 秒,随后是缓慢超极化相,幅度约为 200 - 800 μV,持续时间为 1 - 3 秒。

  3. 在重复刺激期间,低频(低于 5 次/秒)时总和导致总体超极化,高频时导致总体去极化。对 RGC 进行非常高频率(25 次/秒)的刺激可能会在 LGC 中引发一个峰电位。

  4. 双脉冲刺激显示,间隔越短,对去极化相和超极化相的影响就越大。这些影响是渐进的,并且两个相中不会出现一个相消失的情况,而如果 BPSP 是抑制性突触后电位(IPSP)和兴奋性突触后电位(EPSP)的复合物,可能会出现这种情况。

  5. 通过第二个微电极人为施加 LGC 极化的影响表明,BPSP 的去极化相和超极化相均由化学传递机制产生,但不能排除电传递。

  6. 箭毒对 BPSP 没有影响,因此排除了胆碱能传递机制。向 LGC 胞体中注入氯离子似乎不会改变 BPSP,因此得出结论,超极化相与同一细胞的 IPSP 不同。

  7. 刺激 LGC 后,在 RGC 中未记录到突触电位,只有一个标本例外,该标本中 RGC 胞体位于右侧胸膜神经节。在这种情况下,刺激另一个巨细胞时,两个巨细胞中记录到的突触电位均呈双相形式。

  8. 得出结论,BPSP 是一个单一的单突触电位,是这两个巨细胞组织的一个特征。