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STIMULUS-SECRETION COUPLING IN A NEUROSECRETORY ORGAN: THE ROLE OF CALCIUM IN THE RELEASE OF VASOPRESSIN FROM THE NEUROHYPOPHYSIS.神经分泌器官中的刺激-分泌偶联:钙在神经垂体释放血管加压素中的作用。
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CALCIUM MOVEMENT IN THE NEUROHYPOPHYSIS OF THE RAT AND ITS RELATION TO THE RELEASE OF VASOPRESSIN.大鼠神经垂体中的钙运动及其与血管加压素释放的关系
J Physiol. 1964 Jul;172(1):19-30. doi: 10.1113/jphysiol.1964.sp007400.
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Changes in potassium concentration around motor nerve terminals, produced by current flow, and their effects on neuromuscular transmission.电流引起的运动神经末梢周围钾离子浓度的变化及其对神经肌肉传递的影响。
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Relative efficiency of neural firing patterns for vasopressin release in vitro.体外抗利尿激素释放的神经放电模式的相对效率
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Magnocellular neuropeptidergic terminals in neurohypophysis: rapid glial release of enclosed axons during parturition.神经垂体中的大细胞神经肽能终末:分娩期间包裹轴突的快速胶质释放。
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Modification of potassium movement through the retina of the drone (Apis mellifera male) by glial uptake.通过神经胶质细胞摄取对钾离子在雄蜂视网膜中的移动进行调节。
J Physiol. 1983 Jul;340:157-74. doi: 10.1113/jphysiol.1983.sp014756.
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Changes of extracellular potassium activity induced by electric current through brain tissue in the rat.电流通过大鼠脑组织所诱导的细胞外钾离子活性变化
J Physiol. 1983 Feb;335:375-92. doi: 10.1113/jphysiol.1983.sp014540.
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A study of the mechanisms by which potassium moves through brain tissue in the rat.一项关于钾在大鼠脑组织中移动机制的研究。
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Reversible fatigue of stimulus-secretion coupling in the rat neurohypophysis.大鼠神经垂体中刺激-分泌偶联的可逆性疲劳
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Facilitation of vasopressin release from the neurohypophysis by application of electrical stimuli in bursts. Relevant stimulation parameters.通过成串施加电刺激促进神经垂体释放血管加压素。相关刺激参数。
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大鼠大细胞神经分泌系统激活过程中神经垂体细胞外钾的变化

Extracellular potassium changes in the rat neurohypophysis during activation of the magnocellular neurosecretory system.

作者信息

Leng G, Shibuki K

机构信息

AFRC Institute of Animal Physiology and Genetics Research, Babraham, Cambridge.

出版信息

J Physiol. 1987 Nov;392:97-111. doi: 10.1113/jphysiol.1987.sp016771.

DOI:10.1113/jphysiol.1987.sp016771
PMID:2451734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1192295/
Abstract
  1. Potassium-sensitive microelectrodes were used to measure extracellular [K+] in the isolated rat neurohypophysis maintained in vitro. Electrical stimulation of the neurohypophysial stalk (20 Hz 5 s) increased the inferred extracellular [K+] by 9.2 +/- 0.4 mM (mean +/- S.E. of mean; n = 21). 2. Veratridine (10 microM) enhanced the response to stalk stimulation, and at a higher concentration (50 microM) increased extracellular [K+] in the absence of stimulation. By contrast, tetrodotoxin (1 microM) blocked the [K+] increase completely and reversibly in each of five experiments, indicating that the increase was a consequence of action potential generation. 3. At the end of brief periods of stimulation, the raised extracellular [K+] returned to pre-stimulation levels within 30 s. In the presence of ouabain (100 microM), the recovery was slower: the half-decay time was extended by 150-300% in each of three experiments. 4. Replacement of calcium in the medium with cobalt, cadmium or magnesium reduced the amplitude of the [K+] increase by 26-30%, indicating that the [K+] increase was largely independent of events subsequent to evoked release of hormone and/or transmitters. 5. Potassium-sensitive microelectrodes were placed in the neurohypophysis of rats anaesthetized with urethane. Electrical stimulation of the pituitary stalk (50 Hz, 5 s) produced transient voltage increases of 7.6 +/- 0.9 mV (mean +/- S.E. of mean of seven experiments). These voltage increases were similar in magnitude to the response of the electrodes to the addition of 7.6 +/- 1.0 mM-K+ to rat plasma. 6. In seven lactating rats, the suckling of a litter of hungry pups evoked periodic reflex milk ejections, as detected by increases in intramammary pressure. Potassium-sensitive microelectrodes in the neurohypophysis recorded transient voltage increases prior to each milk ejection (0.4-5.5 mV). Each increase preceded an increase in intramammary pressure by 12-30 s. 7. Thus synchronized high-frequency activation of magnocellular neurones can produce large changes in extracellular [K+]. The implications of these findings for stimulus-secretion coupling in the neurohypophysis are discussed in the light of previous reports that hormone release from the neurohypophysis is highly dependent on the frequency and pattern of electrical stimulation.
摘要
  1. 采用钾敏感微电极测量体外培养的离体大鼠神经垂体细胞外的[K⁺]浓度。电刺激神经垂体柄(20赫兹,持续5秒)使推测的细胞外[K⁺]浓度增加了9.2±0.4毫摩尔/升(平均值±平均标准误;n = 21)。2. 藜芦碱(10微摩尔)增强了对柄部刺激的反应,在较高浓度(50微摩尔)时,即使没有刺激也会使细胞外[K⁺]浓度升高。相比之下,在五个实验中,河豚毒素(1微摩尔)完全且可逆地阻断了[K⁺]浓度的升高,表明这种升高是动作电位产生的结果。3. 在短暂刺激结束时,升高的细胞外[K⁺]浓度在30秒内恢复到刺激前水平。在哇巴因(100微摩尔)存在的情况下,恢复较慢:在三个实验中,每个实验的半衰期延长了150 - 300%。4. 用钴、镉或镁替代培养基中的钙,使[K⁺]浓度升高的幅度降低了26 - 30%,表明[K⁺]浓度的升高在很大程度上与激素和/或递质释放后发生的事件无关。5. 将钾敏感微电极置于用乌拉坦麻醉的大鼠的神经垂体中。电刺激垂体柄(50赫兹,5秒)产生了7.6±0.9毫伏的瞬时电压升高(七个实验的平均值±平均标准误)。这些电压升高的幅度与电极对向大鼠血浆中添加7.6±1.0毫摩尔/升钾的反应相似。6. 在七只泌乳大鼠中,一窝饥饿幼崽的吸吮引发了周期性的反射性乳汁喷射,通过乳内压升高检测到。神经垂体中的钾敏感微电极在每次乳汁喷射前(0.4 - 5.5毫伏)记录到瞬时电压升高。每次升高比乳内压升高提前12 - 30秒。7. 因此,大细胞神经元的同步高频激活可使细胞外[K⁺]浓度产生大幅变化。根据先前关于神经垂体激素释放高度依赖电刺激频率和模式的报道,讨论了这些发现对神经垂体刺激 - 分泌偶联的意义。