Randle J C, Bourque C W, Renaud L P
Brain Res. 1984 Jul 30;307(1-2):374-8. doi: 10.1016/0006-8993(84)90499-2.
Extracellular recordings from 141 rat supraoptic nucleus neurons maintained in vitro in a perfused hypothalamic explant indicated that the excitability of 85% of cells was enhanced by the addition of 10-200 microM norepinephrine (NE) and the alpha-agonist methoxamine (MOXY), but not by isoproterenol, to the perfusion medium or by pressure application. Similar responses were observed from 7 cells maintained in synaptic isolation in medium containing 15 mM Mg2+. At the lowest effective concentration (10 microM), NE and MOXY induced bursting activity without an overall increase in firing frequency; at higher concentrations an initial increase in firing frequency was followed by the appearance of phasic activity patterns. The actions of NE and MOXY were reversibly blocked by administration of the alpha-adrenergic antagonists phenoxybenzamine (1-10 microM), yohimbine (greater than 10 microM) and irreversibly blocked by prazosin (10 nM-1 microM). These observations suggest that NE has a predominantly facilitatory role to enhance the excitability and promote bursting activity in supraoptic neurosecretory neurons through an alpha-1 adrenoreceptor mechanism.
对141个在灌注的下丘脑外植体中体外培养的大鼠视上核神经元进行的细胞外记录表明,向灌注培养基中添加10 - 200微摩尔去甲肾上腺素(NE)和α激动剂甲氧明(MOXY),而非异丙肾上腺素,或通过压力施加,可增强85%细胞的兴奋性。在含有15毫摩尔镁离子的培养基中,对7个保持突触隔离的细胞也观察到了类似反应。在最低有效浓度(10微摩尔)时,NE和MOXY诱导爆发活动,但放电频率没有整体增加;在较高浓度时,放电频率先出现初始增加,随后出现相位活动模式。NE和MOXY的作用可被α肾上腺素能拮抗剂酚苄明(1 - 10微摩尔)、育亨宾(大于10微摩尔)可逆性阻断,被哌唑嗪(10纳摩尔 - 1微摩尔)不可逆性阻断。这些观察结果表明,NE主要通过α1肾上腺素能受体机制发挥促进作用,增强视上神经分泌神经元的兴奋性并促进爆发活动。