Single neurohypophyses from male rats were maintained in an in vitro perifusion chamber. Ion-sensitive microelectrodes were introduced into the tissue to measure changes in [K+]o and [Ca2+]o during electrical stimulation. 2. Electrical stimulation at 6 Hz for 1 min and 30 Hz for 12 s raised [K+]o by 5.4 +/- 0.4 and 13.5 +/- 0.5 mM (mean +/- S.E.M., n = 8) respectively. To investigate the effects of raised [K+]o on the excitability of the neurosecretory terminals, stimulations were repeated in media of altered K+ concentration. The increase in [K+]o evoked by 6 Hz stimulation was elevated in 10 mM-K+ medium (133% of that in 5 mM-K+ medium) and reduced in 0 mM-K+ medium and in 25 mM-K+ medium. Thus it appeared that stimulus-induced changes in [K+]o might enhance the excitability of the tissue during electrical activation. 3. To test this hypothesis, we measured the field potential responses evoked by 0.5 Hz stimulation in media of different K+ concentrations. The size of the field potential was enhanced in 10 mM-K+ medium and depressed in 0 mM-K+ medium and in 25 mM-K+ medium. 4. Electrical stimulation (6 Hz, 1 min) decreased [Ca2+]o by 10.9 +/- 1.8% (n = 6). This decrease was absent in the presence of 1 microM-tetrodotoxin or 1 mM-cadmium. Again, the [Ca2+] response to stimulation was enhanced in 10 mM-K+ medium and depressed in 0 mM-K+ medium or 25 mM-K+ medium. 5. The release of vasopressin and oxytocin evoked by stimulation at 6 or 30 Hz from isolated neurohypophyses was measured by radioimmunoassay in a separate series of experiments. Stimulation at 30 Hz for 1 min released 5- to 6-fold more hormone than stimulation at 6 Hz for 5 min. Release evoked by 6 Hz stimulation was enhanced in 15 mM-K+ medium and depressed in 25 mM-K+ medium. 6. We conclude that the rise in [K+]o that accompanies high-frequency activation of axons and terminals in the neurohypophysis contributes to the facilitation of hormone release with increasing frequencies of stimulation, and in particular to the efficiency of the milk-ejection burst discharge of oxytocin neurones for evoking oxytocin release.
摘要
将雄性大鼠的单个神经垂体置于体外灌流室中。将离子敏感微电极插入组织,以测量电刺激期间细胞外钾离子浓度([K+]o)和细胞外钙离子浓度([Ca2+]o)的变化。2. 6 Hz电刺激1分钟和30 Hz电刺激12秒分别使[K+]o升高5.4±0.4和13.5±0.5 mM(平均值±标准误,n = 8)。为研究升高的[K+]o对神经分泌终末兴奋性的影响,在改变钾离子浓度的培养基中重复进行刺激。6 Hz刺激引起的[K+]o升高在10 mM - K+培养基中升高(为5 mM - K+培养基中的133%),在0 mM - K+培养基和25 mM - K+培养基中降低。因此,似乎刺激诱导的[K+]o变化可能在电激活期间增强组织的兴奋性。3. 为验证这一假设,我们测量了在不同钾离子浓度培养基中0.5 Hz刺激诱发的场电位反应。场电位大小在10 mM - K+培养基中增强,在0 mM - K+培养基和25 mM - K+培养基中降低。4. 6 Hz电刺激(1分钟)使[Ca2+]o降低10.9±1.8%(n = 6)。在存在1 μM河豚毒素或1 mM镉的情况下,这种降低不存在。同样,对刺激的[Ca2+]反应在10 mM - K+培养基中增强,在0 mM - K+培养基或25 mM - K+培养基中降低。5. 在另一系列实验中,通过放射免疫测定法测量了6 Hz或30 Hz刺激从分离的神经垂体诱发的血管加压素和催产素释放。30 Hz刺激1分钟释放的激素比6 Hz刺激5分钟多5至6倍。6 Hz刺激诱发的释放在15 mM - K+培养基中增强,在25 mM - K+培养基中降低。6. 我们得出结论,神经垂体中轴突和终末高频激活时伴随的[K+]o升高有助于随着刺激频率增加促进激素释放,特别是有助于催产素神经元的射乳爆发性放电诱发催产素释放的效率。