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1
Increasing quantal size at the mouse neuromuscular junction and the role of choline.增加小鼠神经肌肉接头处的量子大小及胆碱的作用。
J Physiol. 1991 Feb;433:677-704. doi: 10.1113/jphysiol.1991.sp018450.
2
Nicotinic agonists antagonize quantal size increases and evoked release at frog neuromuscular junction.烟碱样激动剂可拮抗蛙神经肌肉接头处量子大小的增加和诱发释放。
J Physiol. 1993 Aug;468:567-89. doi: 10.1113/jphysiol.1993.sp019789.
3
Pretreatment with hypertonic solutions increases quantal size at the frog neuromuscular junction.用高渗溶液进行预处理可增加青蛙神经肌肉接头处的量子大小。
J Neurophysiol. 1987 May;57(5):1536-54. doi: 10.1152/jn.1987.57.5.1536.
4
Vesicle size and transmitter release at the frog neuromuscular junction when quantal acetylcholine content is increased or decreased.当量子化乙酰胆碱含量增加或减少时,青蛙神经肌肉接头处的囊泡大小与递质释放。
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Down-regulation of quantal size at frog neuromuscular junctions: possible roles for elevated intracellular calcium and for protein kinase C.青蛙神经肌肉接头处量子大小的下调:细胞内钙升高和蛋白激酶C的可能作用。
J Neurobiol. 1991 Mar;22(2):204-14. doi: 10.1002/neu.480220210.
6
Repetitive nerve stimulation decreases the acetylcholine content of quanta at the frog neuromuscular junction.重复神经刺激会降低青蛙神经肌肉接头处量子的乙酰胆碱含量。
J Physiol. 2001 May 1;532(Pt 3):637-47. doi: 10.1111/j.1469-7793.2001.0637e.x.
7
The packing of acetylcholine into quanta at the frog neuromuscular junction is inhibited by increases in intracellular sodium.细胞内钠含量的增加会抑制青蛙神经肌肉接头处乙酰胆碱向量子的包装。
Pflugers Arch. 1988 Aug;412(3):258-63. doi: 10.1007/BF00582506.
8
Transmitter packaging at frog neuromuscular junctions exposed to anticholinesterases; the role of second-stage acetylcholine loading.暴露于抗胆碱酯酶的青蛙神经肌肉接头处的递质包装;第二阶段乙酰胆碱装载的作用。
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Synaptic depression in frog neuromuscular junction.青蛙神经肌肉接头处的突触抑制
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The effects of L-vesamicol, an inhibitor of vesicular acetylcholine uptake, on two populations of miniature endplate currents at the snake neuromuscular junction.囊泡乙酰胆碱摄取抑制剂L-维司米克对蛇神经肌肉接头处两种微小终板电流的影响。
Neuroscience. 1990;35(1):145-56. doi: 10.1016/0306-4522(90)90129-r.

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Acetylcholine receptors in the equatorial region of intrafusal muscle fibres modulate mouse muscle spindle sensitivity.肌梭内纤维赤道区的乙酰胆碱受体调节小鼠肌梭敏感性。
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Role of acetylcholinesterase on the structure and function of cholinergic synapses: insights gained from studies on knockout mice.乙酰胆碱酯酶在胆碱能突触的结构和功能中的作用:敲除小鼠研究获得的见解。
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Excitatory-inhibitory imbalance in hypoglossal neurons during the critical period of postnatal development in the rat.大鼠发育后期关键期舌下神经元的兴奋-抑制失衡。
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Motor neuron-specific overexpression of the presynaptic choline transporter: impact on motor endurance and evoked muscle activity.运动神经元特异性过表达突触前胆碱转运体:对运动耐力和诱发肌肉活动的影响。
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Repetitive nerve stimulation decreases the acetylcholine content of quanta at the frog neuromuscular junction.重复神经刺激会降低青蛙神经肌肉接头处量子的乙酰胆碱含量。
J Physiol. 2001 May 1;532(Pt 3):637-47. doi: 10.1111/j.1469-7793.2001.0637e.x.
6
Accounting for the shapes and size distributions of miniature endplate currents.考虑微型终板电流的形状和大小分布。
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7
Bromoacetylcholine and acetylcholinesterase introduced via liposomes into motor nerve endings block increases in quantal size.通过脂质体引入运动神经末梢的溴乙酰胆碱和乙酰胆碱酯酶可阻止量子大小的增加。
Pflugers Arch. 1996 Jul;432(3):413-8. doi: 10.1007/s004240050152.
8
Spontaneous and uniquantal-evoked endplate currents in normal frogs are indistinguishable.正常青蛙的自发终板电流和单量子诱发终板电流无法区分。
J Physiol. 1996 Apr 1;492 ( Pt 1)(Pt 1):155-62. doi: 10.1113/jphysiol.1996.sp021297.
9
Nicotinic agonists antagonize quantal size increases and evoked release at frog neuromuscular junction.烟碱样激动剂可拮抗蛙神经肌肉接头处量子大小的增加和诱发释放。
J Physiol. 1993 Aug;468:567-89. doi: 10.1113/jphysiol.1993.sp019789.
10
Effects of activators and inhibitors of protein kinase A on increases in quantal size at the frog neuromuscular junction.蛋白激酶A激活剂和抑制剂对青蛙神经肌肉接头处量子大小增加的影响。
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本文引用的文献

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Is hyperosmotic neurosecretion from motor nerve endings a calcium-dependent process?运动神经末梢的高渗性神经分泌是一个钙依赖过程吗?
Nature. 1977 May 12;267(5607):170-2. doi: 10.1038/267170a0.
2
An analysis of the end-plate potential recorded with an intracellular electrode.用细胞内电极记录的终板电位分析。
J Physiol. 1951 Nov 28;115(3):320-70. doi: 10.1113/jphysiol.1951.sp004675.
3
PRESYNAPTIC ACTION OF HEMICHOLINIUM AT THE NEUROMUSCULAR JUNCTION.毒扁豆碱在神经肌肉接头处的突触前作用。
J Physiol. 1965 Apr;177(3):463-82. doi: 10.1113/jphysiol.1965.sp007605.
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On the factors which determine the amplitude of the miniature end-plate potential.论决定微小终板电位幅度的因素。
J Physiol. 1957 Jul 11;137(2):267-78. doi: 10.1113/jphysiol.1957.sp005811.
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Quantal components of the end-plate potential.终板电位的量子成分。
J Physiol. 1954 Jun 28;124(3):560-73. doi: 10.1113/jphysiol.1954.sp005129.
6
The timing of channel opening during miniature end-plate currents.微小终板电流期间通道开放的时间
Brain Res. 1981 Oct 26;223(1):185-9. doi: 10.1016/0006-8993(81)90821-0.
7
Inhibition of [3H]acetylcholine active transport by tetraphenylborate and other anions.四苯硼酸盐及其他阴离子对[3H]乙酰胆碱主动转运的抑制作用。
Mol Pharmacol. 1983 Jul;24(1):55-9.
8
Pharmacological characterization of the acetylcholine transport system in purified Torpedo electric organ synaptic vesicles.纯化的电鳐电器官突触小泡中乙酰胆碱转运系统的药理学特性
Mol Pharmacol. 1983 Jul;24(1):48-54.
9
Presynaptic, facilitatory effects of the corticosteroid dexamethasone in rat diaphragm: modulation by beta-bungarotoxin.皮质类固醇地塞米松对大鼠膈肌的突触前促进作用:由β-银环蛇毒素调节
Brain Res. 1984 Mar 5;294(2):315-25. doi: 10.1016/0006-8993(84)91043-6.
10
Independent release of supranormal acetylcholine quanta at the rat neuromuscular junction.大鼠神经肌肉接头处超常乙酰胆碱量子的独立释放
Neuroscience. 1982 Jan;7(1):21-4. doi: 10.1016/0306-4522(82)90149-x.

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.

DOI:10.1113/jphysiol.1991.sp018450
PMID:1841963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1181395/
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)