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增加小鼠神经肌肉接头处的量子大小及胆碱的作用。

Increasing quantal size at the mouse neuromuscular junction and the role of choline.

作者信息

Yu S P, Van der Kloot W

机构信息

Department of Physiology, SUNY, Stony Brook 11794.

出版信息

J Physiol. 1991 Feb;433:677-704. doi: 10.1113/jphysiol.1991.sp018450.

Abstract
  1. In frog a variety of treatments have been shown to increase quantal size at the neuromuscular junction (NMJ), apparently by releasing more acetylcholine (ACh) per quantum. The present experiments were undertaken to see whether similar changes occur at the mouse NMJ. 2. None of the hormones tested, adrenaline, insulin or corticosteroids, significantly increased quantal size at the mouse NMJ. 3. Soaking diaphragms in hypertonic solution (about 475 mosmol/kg) for 15-30 min roughly doubled the size of miniature endplate potentials (MEPPs), miniature endplate currents (MEPCs), and uniquantal endplate potentials (EPPs). We will refer to these as 'large quanta'. Note that all of the measurements were made after returning the preparation to normal (Tyrode) solution. 4. In frog hypertonic solution made with sodium gluconate replacing NaCl increases quantal size four- rather than two-fold. In mouse there was little difference in the effects of solutions made with the two anions. In Cl(-)-free hypertonic solution, made with sodium gluconate and SO4(2-) solutions, quantal size increase is somewhat less, so there may be a role for Cl- in enlarging quantal size. 5. After hypertonic treatment, quantal size remained elevated for at least 1 h and then gradually declined back to usual levels. The data suggest a gradual decrease in mean quantal size, rather than the appearance of a new subpopulation of smaller quanta. 6. Hypertonic treatment did not change the endplate depolarization in response to ionophoretically applied ACh. This suggests that the increased quantal size is not due to a postsynaptic change. Large MEPP's disappear in the presence of tubocurarine and reappear when the drug is washed away. 7. Vesamicol is an inhibitor of active ACh uptake into isolated synaptic vesicles. 5 microM-vesamicol has no detectable postjunctional effect. However, when vesamicol was included in the Tyrode and the hypertonic solutions the increase in quantal size was blocked. This is further evidence that the large quanta are produced by the release of more ACh per quantum. 8. Even when added after the hypertonic treatment, vesamicol soon decreased quantal size back to the normal level. Two other inhibitors of active ACh uptake into vesicles, tetraphenylboron (TPB) and hexanitrodiphenylamine (HNPA) also decreased quantal size after hypertonic treatment, apparently by a presynaptic action. This suggests that the additional ACh that produces large miniatures may be incorporated into the quanta shortly before release.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在青蛙中,已证明多种处理方法可增加神经肌肉接头(NMJ)处的量子大小,显然是通过每个量子释放更多的乙酰胆碱(ACh)。进行本实验是为了观察小鼠NMJ处是否发生类似变化。2. 所测试的激素,肾上腺素、胰岛素或皮质类固醇,均未显著增加小鼠NMJ处的量子大小。3. 将膈肌浸泡在高渗溶液(约475毫渗摩尔/千克)中15 - 30分钟,可使微小终板电位(MEPPs)、微小终板电流(MEPCs)和单量子终板电位(EPPs)的大小大致翻倍。我们将这些称为“大量子”。请注意,所有测量均在将标本恢复到正常(台氏)溶液后进行。4. 在青蛙中,用葡萄糖酸钠替代氯化钠制成的高渗溶液可使量子大小增加四倍而非两倍。在小鼠中,两种阴离子制成的溶液效果差异不大。在用葡萄糖酸钠和硫酸根(SO4(2-))溶液制成的无氯高渗溶液中,量子大小增加幅度稍小,因此氯离子可能在扩大量子大小方面起作用。5. 高渗处理后,量子大小至少在1小时内保持升高,然后逐渐下降至正常水平。数据表明平均量子大小逐渐减小,而非出现新的较小量子亚群。6. 高渗处理并未改变离子电泳施加ACh时的终板去极化。这表明量子大小增加并非由于突触后变化。在筒箭毒碱存在下,大MEPP消失,药物洗脱后重新出现。7. 囊泡胺是一种抑制ACh主动摄取到分离突触小泡中的抑制剂。5微摩尔囊泡胺没有可检测到的突触后效应。然而,当囊泡胺包含在台氏液和高渗溶液中时,量子大小的增加被阻断。这进一步证明大量子是由每个量子释放更多的ACh产生的。8. 即使在高渗处理后添加,囊泡胺也会很快使量子大小降至正常水平。另外两种抑制ACh主动摄取到小泡中的抑制剂,四苯基硼(TPB)和六硝基二苯胺(HNPA),在高渗处理后也会降低量子大小,显然是通过突触前作用。这表明产生大微小电位的额外ACh可能在释放前不久被纳入量子中。(摘要截短至400字)

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