Summerlee A J, Lincoln D W
J Endocrinol. 1981 Aug;90(2):255-65. doi: 10.1677/joe.0.0900255.
A method is described for making extracellular recordings of the spontaneous activity of single hypothalamic neurones in unanaesthetized, freely moving, lactating rats using chronically implanted micro-wire electrodes. Extracellular recordings taken from individual neurones were maintained for periods of between 1 and 12 days. These records were not affected by any normal movement of the animal. As several micro-wires were implanted into each animal it was possible to make simultaneous recordings from several different hypothalamic sites in the same animal. Some recordings were identified as those from magnocellular neurones in the paraventricular nucleus on the basis of antidromic invasion after electrical stimulation of the neurohypophysis. Milk ejection in response to the prolonged sucking of ten or more pups was intermittent, and individual milk ejections recurred at intervals of 2-10 min throughout each period of nursing. The rise in intramammary pressure at milk ejection was associated with a vigorous extensor response from the pups. This was monitored by radar to provide an index of milk ejection in the unanaesthetized rat. Eleven antidromically identified neurones were recorded through 321 milk ejections. Eight of these neurones displayed a transient (2-6s) and very substantial acceleration in discharge at the time predicted for oxytocin release, i.e. 10-12s before milk ejection. The background discharge of these cells was 0.1-2.6 action potentials/s; this increased to 16-50 action potentials/s during the brief period of accelerated activity. Twenty-five neurones were studied during 365 milk ejections in rats which did not have a stimulating electrode implanted in the neurohypophysis. Thirteen of these neurones displayed a burst of high frequency discharge before each milk ejection, similar to that described for the antidromically identified neurones. Two of the non-responsive cells displayed a phasic pattern of discharge, characteristic of vasopressinergic neurone discharge recorded in anaesthetized rats. These observations of putative oxytocinergic neurones in unanaesthetized, freely moving rats are identical with those previously made on anaesthetized rats, and establish that the high frequency burst of electrical activity displayed by magnocellular neurones some 10-12s before milk ejection is responsible for oxytocin release under normal physiological circumstances.
本文描述了一种使用慢性植入的微丝电极,在未麻醉、自由活动的泌乳大鼠中对单个下丘脑神经元的自发活动进行细胞外记录的方法。从单个神经元获取的细胞外记录持续了1至12天。这些记录不受动物任何正常活动的影响。由于每只动物植入了几根微丝,因此可以在同一只动物的几个不同下丘脑部位同时进行记录。在对神经垂体进行电刺激后,根据逆向入侵,一些记录被确定为来自室旁核大细胞神经元的记录。对十只或更多幼崽长时间吸吮的反应中,乳汁排出是间歇性的,并且在每个哺乳期间,个体乳汁排出以2至10分钟的间隔反复出现。乳汁排出时乳腺内压力的升高与幼崽强烈的伸展反应相关。通过雷达对其进行监测,以提供未麻醉大鼠乳汁排出的指标。通过321次乳汁排出记录了11个经逆向鉴定的神经元。其中8个神经元在预测催产素释放的时间,即乳汁排出前10至12秒,显示出放电的短暂(2至6秒)且非常显著的加速。这些细胞的背景放电为0.1至2.6个动作电位/秒;在短暂的加速活动期间,这增加到16至50个动作电位/秒。在没有将刺激电极植入神经垂体的大鼠的365次乳汁排出过程中,研究了25个神经元。其中13个神经元在每次乳汁排出前显示出高频放电爆发,类似于经逆向鉴定的神经元所描述的情况。两个无反应的细胞显示出阶段性放电模式,这是在麻醉大鼠中记录到的加压素能神经元放电的特征。在未麻醉、自由活动的大鼠中对假定的催产素能神经元的这些观察结果与之前在麻醉大鼠中所做的观察结果相同,并证实了大细胞神经元在乳汁排出前约10至12秒显示的高频电活动爆发在正常生理情况下负责催产素的释放。