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去甲肾上腺素对大鼠膈肌神经末梢的作用。

Noradrenaline action on nerve terminal in the rat diaphragm.

作者信息

Kuba K, Tomita T

出版信息

J Physiol. 1971 Aug;217(1):19-31. doi: 10.1113/jphysiol.1971.sp009557.

Abstract
  1. The mechanism by which noradrenaline increases the release of transmitter from the nerve terminal was investigated in the rat diaphragm.2. Increase of the frequency of the miniature end-plate potential (m.e.p.p.) was exponential when plotted against the intensity of a constant current which depolarized the nerve terminal. Noradrenaline (5 x 10(-6) g/ml.) did not change the slope of the curve showing the relationship between the logarithm of the frequency of m.e.p.p.s and the depolarizing current (m.e.p.p.-current relationship), but simply shifted the curve along the axis of the current towards weaker intensities.3. End-plate potentials (e.p.p.s) were evoked by passing a brief depolarizing pulse to the nerve terminal in the presence of tetrodotoxin (1 x 10(-7) g/ml.). A sigmoidal relationship was obtained between the amplitude of e.p.p. and the intensity of the current pulse (e.p.p.-current intensity relationship). Noradrenaline (5 x 10(-6) g/ml.) shifted the e.p.p.-current intensity relationship along the axis of the current intensity to smaller values, without any change in the maximum amplitude of e.p.p.s.4. The frequency of m.e.p.p. was increased, as the Ca was raised from 0.01 to 7.5 mM. An increase in Ca beyond the normal concentration (2.5 mM) had no remarkable effect on the action of noradrenaline. However, when Ca was reduced, the action of noradrenaline became weaker.5. A kinetic model in which the transmitter release is modified by the binding of Ca with a specific site in the nerve terminal may explain the results. According to this model, noradrenaline did not change the dissociation constant of the reaction between Ca and the specific site (X), but increased the rate constant of the Ca complex (CaX) for releasing acetylcholine.6. The action of noradrenaline was potentiated when Na was reduced, and suppressed when Mg was increased. The results may be summarized: that noradrenaline augments the probability of release of transmitter quanta from the resting nerve terminals and that this action can be intensified by first raising the probability of release by some other means. Depolarization of the nerve terminals by current, increase of the external Ca concentration, decrease of Na and decrease of Mg are all effective in promoting the action of noradrenaline.
摘要
  1. 在大鼠膈肌中研究了去甲肾上腺素增加神经末梢递质释放的机制。

  2. 当以使神经末梢去极化的恒定电流强度作图时,微小终板电位(m.e.p.p.)频率的增加呈指数关系。去甲肾上腺素(5×10⁻⁶ g/ml)并未改变显示m.e.p.p.频率对数与去极化电流之间关系的曲线斜率(m.e.p.p.-电流关系),而只是使该曲线沿电流轴朝着较弱强度方向移动。

  3. 在存在河豚毒素(1×10⁻⁷ g/ml)的情况下,通过向神经末梢施加一个短暂的去极化脉冲来诱发终板电位(e.p.p.s)。在e.p.p.幅度与电流脉冲强度之间获得了一种S形关系(e.p.p.-电流强度关系)。去甲肾上腺素(5×10⁻⁶ g/ml)使e.p.p.-电流强度关系沿电流强度轴移向较小值,而e.p.p.s的最大幅度没有任何变化。

  4. 随着[Ca]₀从0.01 mM升高到7.5 mM,m.e.p.p.的频率增加。[Ca]₀超过正常浓度(2.5 mM)对去甲肾上腺素的作用没有显著影响。然而,当[Ca]₀降低时,去甲肾上腺素的作用变弱。

  5. 一种动力学模型,其中递质释放通过Ca与神经末梢中一个特定位点的结合而被改变,可能解释这些结果。根据该模型,去甲肾上腺素并未改变Ca与特定位点(X)之间反应的解离常数,但增加了Ca复合物(CaX)释放乙酰胆碱的速率常数。

  6. 当[Na]₀降低时,去甲肾上腺素的作用增强,而当[Mg]₀增加时,其作用受到抑制。结果可以总结为:去甲肾上腺素增加了静息神经末梢释放递质量子的概率,并且这种作用可以通过首先以其他一些方式提高释放概率而得到增强。通过电流使神经末梢去极化、增加细胞外Ca浓度、降低Na浓度和降低Mg浓度都有效地促进了去甲肾上腺素的作用。

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