Bourque C W, Renaud L P
J Physiol. 1984 Apr;349:631-42. doi: 10.1113/jphysiol.1984.sp015178.
Extracellular recordings were obtained in vitro from supraoptic neurones in an explant of rat hypothalamus maintained viable through intravascular perfusion with artificial media. The spontaneous activity observed from 64% of cells included continuously active neurones (mean frequency 3.2 +/- 0.8 Hz) located throughout the nucleus, and phasically active neurones (8.6 +/- 0.6 Hz) located predominantly in the caudal half of the nucleus. Supraoptic neurones displayed antidromic activation (latency range 6.5-18.2 ms) following stimulation of the pituitary stalk and orthodromic excitatory or inhibitory responses following stimulation in the anteroventral third ventricular (AV3V) region. Synaptic responses were reversibly abolished during perfusion with media containing 12 mM-Mg2+. A 15-40 mosmol/l increase in the osmotic pressure of the perfusion media, through addition of NaCl, sucrose or mannitol, prompted nineteen of twenty-three cells to increase their discharge frequency. The patterns of response included the induction or simple increase in continuous firing frequency, the induction or enhancement of phasic or bursting activity and a change from continuous to phasic activity. Similar responses to an osmotic stimulus were obtained from thirteen of twenty-one supraoptic neurones, including two phasic neurones, where synaptic activity had been abolished during perfusion with 12 mM-Mg2+. Osmosensitivity appeared to be selective for supraoptic cells; no significant change in firing frequency was observed from any of six cells recorded in the lateral hypothalamus or thirteen cells recorded in the medial hypothalamus during exposure to a change in osmotic pressure of +20 to +40 mosmol/l, using either control media (seven cells) or media containing 12 mM-Mg2+ (twelve cells). These observations indicate that supraoptic neurones maintained in vitro can display spontaneous, antidromie , orthodromic and osmotically induced activity patterns identical to those observed with in vivo recordings. The persistence of a reduced osmosensitivity among supraoptic neurones in the absence of synaptic transmission indicates that although these cells can function as osmoreceptors, their osmosensitivity may be enhanced through synaptic input from adjacent neurones, possibly located in the AV3V area. The presence of phasic activity among supraoptic neurones maintained in media where synaptic transmission has been abolished suggests that the mechanisms responsible for such activity patterns are endogenous membrane properties of a subpopulation of supraoptic neurones.
通过向大鼠下丘脑外植体的血管内灌注人工培养基以维持其存活,从而在体外获得视上核神经元的细胞外记录。在64%的细胞中观察到的自发活动包括位于整个视上核的持续活动神经元(平均频率3.2±0.8Hz)和主要位于视上核后半部的相位性活动神经元(8.6±0.6Hz)。刺激垂体柄后,视上核神经元出现逆向激活(潜伏期范围6.5 - 18.2毫秒),刺激前腹侧第三脑室(AV3V)区域后出现顺向兴奋性或抑制性反应。在用含12 mM - Mg²⁺的培养基灌注期间,突触反应可逆性消失。通过添加氯化钠、蔗糖或甘露醇使灌注培养基的渗透压升高15 - 40毫渗摩尔/升,促使23个细胞中的19个增加其放电频率。反应模式包括持续放电频率的诱导或简单增加、相位性或爆发性活动的诱导或增强以及从持续活动到相位性活动的转变。在21个视上核神经元中的13个中观察到对渗透压刺激的类似反应,其中包括2个相位性神经元,在用12 mM - Mg²⁺灌注期间突触活动已被消除。渗透压敏感性似乎对视上核细胞具有选择性;在使用对照培养基(7个细胞)或含12 mM - Mg²⁺的培养基(12个细胞)将渗透压改变+20至+40毫渗摩尔/升的过程中,在下丘脑外侧记录的6个细胞或下丘脑内侧记录的13个细胞中,未观察到放电频率有显著变化。这些观察结果表明,体外培养的视上核神经元可以表现出与体内记录中观察到的相同的自发、逆向、顺向和渗透压诱导的活动模式。视上核神经元在没有突触传递的情况下渗透压敏感性降低的持续存在表明,尽管这些细胞可以作为渗透压感受器发挥作用,但其渗透压敏感性可能通过来自相邻神经元(可能位于AV3V区域)的突触输入而增强。在已消除突触传递的培养基中培养的视上核神经元中存在相位性活动,这表明负责这种活动模式的机制是视上核神经元亚群的内源性膜特性。