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降低外部钠浓度对蟹肌纤维细胞内钠活性的影响。

The effect of lowering external sodium on the intracellular sodium activity of crab muscle fibres.

作者信息

Vaughan-Jones R D

出版信息

J Physiol. 1977 Jan;264(1):239-65. doi: 10.1113/jphysiol.1977.sp011666.

Abstract
  1. Intracellular Na activity, aiNa, was continuously measured in crab (Carcinus maenas) muscle fibres using a recessed-tip Na+ -sensitive glass micro-electrode. Experiments could last up to several hours. AiNa remained stable during prolonged experiments. The mean resting aiNa was 8-4 +/- 0-02 mM (S.E. of mean for eighty-nine fibres) and the mean resting membrane potential was 65-3 mV +/- 0-3 (S.E. of mean for eighty-nine fibres). 2. Reducing [Na]o to 1/10 normal (maintaining ionic strength with equivalent amounts of either Li or Tris) caused a large and rapid fall of aiNa. There appeared to be two components of the effect, a fast and slow. The initial fast rate of decrease was about 3-5 m-mole/min decreasing to half this value in about 1 min. The rate of decrease of aiNa was not linearly related to aiNa. The size of the fast change of aiNa was related to the magnitude of the Na gradient across the membrane. 3. High concentrations (2 x 10-4m) of ouabain caused a very slow rise of aiNa by 1 or 2 mn/hr. This was equivalent to a net Na influx of between 1 and 10 p-mole/cmi. sec, depending on whether or not a correction was applied to account for the increased surface area of the fibre caused by the invaginating cleft system. 4. The response to low Nso was virtually insensitive to the removal of Ko or to prolonged reatment with high concentrations of ouabain (2 x 10-4 m; 100 min) and so could not readily be attributed to active Na/K pumping. 5. The response of aiNa to low Nao was reversibly inhibited by high concencentrations of Mn (50 mm) and by low concentrations of La (3-1 mm). La itself stimulated a rapid fall of aiNa in normal Nao.
摘要
  1. 使用凹尖型钠离子敏感玻璃微电极连续测量蟹(Carcinus maenas)肌肉纤维中的细胞内钠离子活性(aiNa)。实验可持续长达数小时。在长时间实验过程中,aiNa保持稳定。平均静息aiNa为8.4±0.02 mM(89根纤维的平均标准误),平均静息膜电位为65.3 mV±0.3(89根纤维的平均标准误)。2. 将[Na]o降至正常水平的1/10(用等量的Li或Tris维持离子强度)会导致aiNa大幅快速下降。这种效应似乎有两个成分,一个快速的和一个缓慢的。最初的快速下降速率约为3 - 5毫摩尔/分钟,在约1分钟内降至该值的一半。aiNa的下降速率与aiNa并非线性相关。aiNa的快速变化大小与跨膜钠梯度的大小有关。3. 高浓度(2×10⁻⁴m)的哇巴因导致aiNa以非常缓慢的速度上升,每小时上升1或2毫摩尔。这相当于净钠内流在1至10皮摩尔/平方厘米·秒之间,这取决于是否对因内陷裂隙系统导致的纤维表面积增加进行校正。4. 对低[Na]o的反应实际上对去除[K]o或用高浓度哇巴因(2×10⁻⁴m;100分钟)长时间处理不敏感,因此不太可能归因于钠钾主动转运。5. aiNa对低[Na]o的反应被高浓度的Mn(50 mM)和低浓度的La(3 - 1 mM)可逆抑制。La本身在正常[Na]o中会刺激aiNa快速下降。

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