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青蛙神经肌肉接头处的突触抑制

Synaptic depression in frog neuromuscular junction.

作者信息

Glavinović M I

出版信息

J Neurophysiol. 1987 Jul;58(1):230-46. doi: 10.1152/jn.1987.58.1.230.

Abstract
  1. The amplitudes of end-plate currents (EPCs) evoked by stimulating the nerve with frequencies ranging from 1 to 5 Hz and the amplitudes of miniature end-plate currents (MEPCs) gradually diminish if choline uptake is blocked by hemicholinium-3 (HC-3, 20 microM). This reduction of EPC amplitudes is predominantly of presynaptic origin, although an observed decrease in MEPC amplitudes suggests that some postsynaptic changes [due to direct action of HC-3 on acetylcholine (ACh) receptors or on open ACh channels] also occurs. 2. Shortening of both EPCs and MEPCs is observed during high-frequency stimulation (5 Hz) in the presence of cholinesterase inhibitor after impairment of ACh synthesis. Shortening of MEPCs probably results from a direct blocking action of HC-3 on open ACh channels, as well as from reduction in quantal size. Shortening of EPCs is more pronounced (EPCs eventually have shorter time courses than MEPCs) and usually does not result from a gradual reduction in the spatial overlap of quantal events (because of reduced quantal content) or from a diminished 'lingering ACh' (ACh that remains in the synaptic cleft between nerve impulses), but rather from a much reduced quantal size of nerve-evoked quanta. 3. It therefore appears that the quanta that are released by nerve stimulation are preferentially filled with newly synthesized ACh. In its absence nerve stimulation leads to secretion of only partially filled quanta. This occurs simultaneously with spontaneous secretion of almost normally filled quanta. Hence it seems that the quantal discharge is not strongly dependent, if at all, on its ACh content. Moreover, the correspondence between the quantal sizes of nerve-evoked and spontaneously released quanta does not remain valid during high-frequency prolonged stimulation. 4. Even with the choline uptake system intact, prolonged high-frequency stimulation leads to a gradual shortening of EPCs and, to a small extent, MEPCs. Shortening of EPCs appears to be mainly a result of a reduction of their quantal size. 5. It is estimated from the shortening of EPCs and the known EPC versus MEPC relationship that the reduction of the quantal sizes of nerve-evoked quanta probably contributes very significantly to synaptic depression that occurs during prolonged high-frequency nerve stimulation.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 用1至5赫兹的频率刺激神经所诱发的终板电流(EPCs)的幅度以及微小终板电流(MEPCs)的幅度,如果用半胱氨酸-3(HC-3,20微摩尔)阻断胆碱摄取,会逐渐减小。EPC幅度的这种降低主要源于突触前,尽管观察到的MEPC幅度降低表明也发生了一些突触后变化[由于HC-3对乙酰胆碱(ACh)受体或开放的ACh通道的直接作用]。2. 在ACh合成受损后,在存在胆碱酯酶抑制剂的情况下,高频刺激(5赫兹)期间观察到EPCs和MEPCs均缩短。MEPCs的缩短可能是由于HC-3对开放的ACh通道的直接阻断作用以及量子大小的减小。EPCs的缩短更为明显(EPCs最终的时间进程比MEPCs短),并且通常不是由于量子事件空间重叠的逐渐减少(由于量子含量减少)或“残留ACh”(神经冲动之间留在突触间隙中的ACh)的减少,而是由于神经诱发量子的量子大小大大减小。3. 因此,似乎神经刺激释放的量子优先填充有新合成的ACh。在其不存在的情况下,神经刺激仅导致部分填充量子的分泌。这与几乎正常填充量子的自发分泌同时发生。因此,似乎量子释放如果根本不强烈依赖于其ACh含量。此外,在高频长时间刺激期间,神经诱发量子和自发释放量子的量子大小之间的对应关系不再成立。4. 即使胆碱摄取系统完整,长时间的高频刺激也会导致EPCs逐渐缩短,并在一定程度上导致MEPCs缩短。EPCs的缩短似乎主要是其量子大小减小的结果。5. 根据EPCs的缩短以及已知的EPC与MEPC关系估计,神经诱发量子的量子大小的减小可能对长时间高频神经刺激期间发生的突触抑制有非常显著的贡献。(摘要截断于400字)

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