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在器官培养的青蛙神经肌肉标本中特定神经末梢处乙酰胆碱的释放。

Acetylcholine release at identified nerve terminals in the organ-cultured frog neuromuscular preparation.

作者信息

Cherki-Vakil R, Meiri H

机构信息

Department of Physiology, Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

J Physiol. 1990 Apr;423:579-92. doi: 10.1113/jphysiol.1990.sp018041.

Abstract
  1. The frog cutaneous pectoris neuromuscular preparation was maintained in organ culture for a few days, at either 24 or 14 degrees C. The synaptic activity of identified nerve terminals was repeatedly examined in order to describe the sequence and time course of changes from normal synaptic activity to a complete synaptic silence. 2. We found that the 'transient stage' (stage II, according to Ko, 1981) consists of at least three distinct periods each characterized by a unique trend of change in synaptic activity. The initial change involved a simultaneous decay of both spontaneous and nerve stimulation-evoked release of acetylcholine (sub-stage II1). Subsequently, the frequency of spontaneous miniature endplate potentials (MEPPs) increased gradually, while the evoked release continued its monotonous decay (sub-stage II2). During the third sub-stage spontaneous MEPPs, but no evoked endplate potentials (EPPs), were observed (sub-stage II3). 3. Statistical properties of acetylcholine release in still-transmitting junctions at sub-stage II2 and in non-transmitting junctions at sub-stage II3 were investigated. MEPPs with skewed amplitude histograms and bursting behaviour were evident at both sub-stages. However, the incidence and the extent of these distortions were higher in the non-transmitting junctions. 4. An inverse relation between the quantal content of evoked release and the rate of spontaneous secretion was found in the transmitting junctions. 5. These results suggest that some of the deterioration of synaptic activity in organ culture is caused by an impairment of the release process itself. Possible cellular mechanisms are discussed.
摘要
  1. 将蛙胸皮神经肌肉标本在24℃或14℃下进行器官培养数天。反复检查已识别神经末梢的突触活性,以描述从正常突触活性到完全突触沉默的变化顺序和时间进程。2. 我们发现,“过渡阶段”(根据Ko,1981年的II期)至少由三个不同时期组成,每个时期的特征是突触活性变化的独特趋势。最初的变化包括乙酰胆碱的自发释放和神经刺激诱发释放同时衰减(II1亚期)。随后,自发微小终板电位(MEPPs)的频率逐渐增加,而诱发释放继续单调衰减(II2亚期)。在第三个亚期,观察到自发MEPPs,但未观察到诱发终板电位(EPPs)(II3亚期)。3. 研究了II2亚期仍在传递的突触和II3亚期不传递的突触中乙酰胆碱释放的统计特性。在两个亚期,具有偏态幅度直方图和爆发行为的MEPPs都很明显。然而,这些扭曲的发生率和程度在不传递的突触中更高。4. 在传递的突触中发现诱发释放的量子含量与自分泌速率之间呈反比关系。5. 这些结果表明,器官培养中突触活性的一些恶化是由释放过程本身的损伤引起的。讨论了可能的细胞机制。

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