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小龙虾神经肌肉接头处短暂超极化脉冲对突触释放的阻断作用。

Blockage of synaptic release by brief hyperpolarizing pulses in the neuromuscular junction of the crayfish.

作者信息

Arechiga H, Cannone A, Parnas H, Parnas I

机构信息

Otto Loewi Center for Cellular and Molecular Neurobiology, Hebrew University of Jerusalem, Israel.

出版信息

J Physiol. 1990 Nov;430:119-33. doi: 10.1113/jphysiol.1990.sp018285.

Abstract
  1. Synaptic currents were evoked at the neuromuscular junction of the deep extensor abdominal muscle of the crayfish by direct depolarization of motor nerve endings. 2. Quantal content and time course of neurotransmitter release were determined from delay histograms of unitary release events recorded with a macropatch clamp technique. 3. Synaptic facilitation was elicited by pairing depolarizing pulses at intervals ranging from 10 to 200 ms. At 14 degrees C the duration of facilitation was about 50 ms. Reducing activity of the Nao(+)-Cai2+ exchange by lowering [Na+]o by 50% resulted in prolonged facilitation, which lasted approximately 150 ms. 4. Normalized synaptic delay histograms at normal [Na+]o and 50% [Na+]o were the same for the first and the facilitated second response, indicating that activity of the Na(+)-Ca2+ exchange does not determine the time course of release. 5. The application of a hyperpolarizing post-pulse after the first depolarizing stimulus reduced release and altered its time course to a similar extent both in normal and in 50% [Na+]o. However, it did not affect the level and the time course of release of the facilitated response. 6. A hyperpolarizing post-pulse given after the first and second pulses of a pair reduced release to the same extent for the two depolarizing pulses. 7. These results indicate that whereas manipulations thought to increase [Ca2+]i (i.e. reducing activity of the Nao(+)-Cai2+ exchange or facilitation) affect the quantal content, they do not influence the time course of release. However, changes of membrane potential do affect the quantal content, and more importantly the time course of release, thus suggesting a contributory role of membrane potential in the control of synaptic release.
摘要
  1. 通过对小龙虾腹部深层伸肌神经肌肉接头处运动神经末梢进行直接去极化,诱发突触电流。2. 采用膜片钳技术记录单位释放事件的延迟直方图,确定神经递质释放的量子含量和时间进程。3. 通过以10至200毫秒的间隔配对去极化脉冲来诱发突触易化。在14摄氏度时,易化持续时间约为50毫秒。将细胞外[Na+]降低50%以降低Na(+)-Ca2+交换活性,导致易化延长,持续约150毫秒。4. 在正常[Na+]o和50%[Na+]o条件下,第一次和易化后的第二次反应的归一化突触延迟直方图相同,表明Na(+)-Ca2+交换活性不决定释放的时间进程。5. 在第一个去极化刺激后施加超极化后脉冲,在正常和50%[Na+]o条件下,均降低了释放并在相似程度上改变了其时间进程。然而,它不影响易化反应的释放水平和时间进程。6. 在一对脉冲的第一个和第二个脉冲后施加超极化后脉冲,对两个去极化脉冲的释放降低程度相同。7. 这些结果表明,虽然被认为增加[Ca2+]i的操作(即降低Na(+)-Ca2+交换活性或易化)会影响量子含量,但它们不影响释放的时间进程。然而,膜电位变化确实会影响量子含量,更重要的是影响释放的时间进程,因此表明膜电位在突触释放控制中起作用。

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