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本文引用的文献

1
The anatomy and innervation of locust skeletal muscle.蝗虫骨骼肌的解剖结构与神经支配
Proc R Soc Lond B Biol Sci. 1955 Jan 27;143(911):281-92. doi: 10.1098/rspb.1955.0011.
2
THE EFFECT ON CRAYFISH MUSCLE OF IONTOPHORETICALLY APPLIED GLUTAMATE.离子电渗法施加谷氨酸对小龙虾肌肉的影响
J Physiol. 1964 Mar;170(2):296-317. doi: 10.1113/jphysiol.1964.sp007332.
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The excitation of spinal neurones by the ionophoretic application of agents which chelate calcium.通过离子电泳施加螯合钙的试剂对脊髓神经元的刺激。
J Neurochem. 1960 Aug;6:1-20. doi: 10.1111/j.1471-4159.1960.tb13443.x.
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Neuromuscular transmission in a locust.蝗虫中的神经肌肉传递。
J Physiol. 1953 Sep;121(3):539-47. doi: 10.1113/jphysiol.1953.sp004963.
5
Single glutamate-activated channels recorded from locust muscle fibres with perfused patch-clamp electrodes.使用灌注式膜片钳电极从蝗虫肌肉纤维记录到的单谷氨酸激活通道。
J Physiol. 1981 Dec;321:195-210. doi: 10.1113/jphysiol.1981.sp013979.
6
Nickel and calcium ions modify the characteristics of the acetylcholine receptor-channel complex at the frog neuromuscular junction.镍离子和钙离子改变青蛙神经肌肉接头处乙酰胆碱受体-通道复合物的特性。
J Physiol. 1980 Feb;299:203-18. doi: 10.1113/jphysiol.1980.sp013120.
7
Effects of high calcium solutions on glutamate sensitivity of crayfish muscle fibres.
Proc R Soc Lond B Biol Sci. 1980 Sep 26;209(1176):415-29. doi: 10.1098/rspb.1980.0103.
8
Depolarization and calcium entry in squid giant axons.枪乌贼巨大轴突中的去极化和钙内流。
J Physiol. 1971 Nov;218(3):709-55. doi: 10.1113/jphysiol.1971.sp009641.
9
The statistical nature of the acetycholine potential and its molecular components.乙酰胆碱电位及其分子成分的统计学性质。
J Physiol. 1972 Aug;224(3):665-99. doi: 10.1113/jphysiol.1972.sp009918.
10
Physiology and ultrastructure of phasic and tonic skeletal muscle fibres in the locust, Schistocerca gregaria.沙漠蝗(Schistocerca gregaria)中相性和紧张性骨骼肌纤维的生理学与超微结构
J Cell Sci. 1972 Mar;10(2):419-41. doi: 10.1242/jcs.10.2.419.

蝗虫神经-肌肉接头处微小兴奋性突触后电流的特性。

Properties of miniature excitatory junctional currents at the locust nerve-muscle junction.

作者信息

Cull-Candy S G, Miledi R

出版信息

J Physiol. 1982 May;326:527-51. doi: 10.1113/jphysiol.1982.sp014210.

DOI:10.1113/jphysiol.1982.sp014210
PMID:6286952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1251492/
Abstract
  1. Miniature excitatory junctional currents (m.e.j.c.s) were examined in conditions where inward current was carried mainly by Na(+) (i.e. in normal medium, Ca(2+)-free medium and Cl(-)-free medium). M.e.j.c.s were also examined in isotonic Ca(2+) where the inward post-synaptic current was carried mainly by Ca(2+).2. In normal medium, mean m.e.j.c. amplitude = 2.34+/-0.05 nA. The decay time constant of m.e.j.c.s (excluding a small percentage with abnormal shapes) was tau(m.e.j.c.) = 2.62+/-0.11 msec (V(m) = -80 mV, T = 22 degrees C). Decay-time was not markedly changed in Ca(2+)-free or Cl(-)-free medium. tau(m.e.j.c.) approaches the life-time of glutamate activated junctional channels.3. Excitatory junctional currents, evoked by nerve impulses, decayed slightly faster than m.e.j.c.s obtained in the same fibres. Extracellularly recorded m.e.j.c.s and voltage-clamped m.e.j.c.s were similar in time course.4. tau(m.e.j.c.) decreased exponentially with membrane hyperpolarization. An e-fold change was produced by 182.+/-24.8 mV change in V(m).5. The dependence of mean m.e.j.c. amplitude on clamp potential showed a slight non-linearity at hyperpolarized levels. The equilibrium potential for transmitter action was close to 0 mV in normal solution as well as in Ca(2+)-free and Cl(-)-free solutions.6. The kinetics of junctional channels are altered in isotonic Ca(2+). M.e.j.c. amplitude was reduced to about one-third normal size; mean m.e.j.c. = 0.74+/-0.03 nA. The decay time becomes markedly briefer, tau(m.e.j.c.) = 1.01+/-0.08 msec, indicating a reduction in mean channel life-time (V(m) = -80 mV, T = 22 degrees C).7. A population of slow time course and composite m.e.j.c.s appear when muscle fibres are hyperpolarized in isotonic Ca(2+), thus producing a prolongation in mean tau(m.e.j.c.). This results from an influence of post-synaptic membrane potential on presynaptic transmitter release. If such m.e.j.c.s are ignored the voltage dependence of tau(m.e.j.c.) of the remaining events is abolished or even reversed indicating that voltage sensitivity of channel life-time is altered in isotonic Ca(2+). The equilibrium potential for transmitter action may be slightly more positive than normal.8. We estimate that a single packet of neurally released transmitter normally opens, on average, 250 ion channels at these junctions.
摘要
  1. 在内向电流主要由Na⁺携带的条件下(即正常培养基、无Ca²⁺培养基和无Cl⁻培养基中)检测微小兴奋性突触后电流(m.e.j.c.s)。也在等渗Ca²⁺中检测m.e.j.c.s,此时内向突触后电流主要由Ca²⁺携带。

  2. 在正常培养基中,平均m.e.j.c.幅度 = 2.34±0.05 nA。m.e.j.c.s的衰减时间常数(不包括一小部分形状异常的)为τ(m.e.j.c.) = 2.62±0.11毫秒(V(m) = -80 mV,T = 22℃)。在无Ca²⁺或无Cl⁻培养基中,衰减时间没有明显变化。τ(m.e.j.c.)接近谷氨酸激活的突触通道的寿命。

  3. 由神经冲动诱发的兴奋性突触后电流的衰减比在相同纤维中获得的m.e.j.c.s稍快。细胞外记录的m.e.j.c.s和电压钳制的m.e.j.c.s在时间进程上相似。

  4. τ(m.e.j.c.)随膜超极化呈指数下降。V(m)变化182.±24.8 mV产生一个e倍变化。

  5. 平均m.e.j.c.幅度对钳制电位的依赖性在超极化水平显示出轻微的非线性。在正常溶液以及无Ca²⁺和无Cl⁻溶液中,递质作用的平衡电位接近0 mV。

  6. 等渗Ca²⁺中突触通道的动力学发生改变。m.e.j.c.幅度降低到正常大小的约三分之一;平均m.e.j.c. = 0.74±0.03 nA。衰减时间明显变短,τ(m.e.j.c.) = 1.01±0.08毫秒,表明平均通道寿命缩短(V(m) = -80 mV,T = 22℃)。

  7. 当肌肉纤维在等渗Ca²⁺中被超极化时,会出现一群慢时间进程和复合的m.e.j.c.s,从而使平均τ(m.e.j.c.)延长。这是由于突触后膜电位对突触前递质释放的影响。如果忽略这些m.e.j.c.s,其余事件的τ(m.e.j.c.)对电压的依赖性将被消除甚至反转,这表明等渗Ca²⁺中通道寿命的电压敏感性发生了改变。递质作用的平衡电位可能比正常情况略正。

  8. 我们估计,在这些突触处,单个神经释放的递质包通常平均打开250个离子通道。