Yamashita H, Yamamoto S, Inenaga K, Kannan H
First Department of Physiology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
J Cardiovasc Pharmacol. 1991;17 Suppl 7:S200-2. doi: 10.1097/00005344-199100177-00057.
Extracellular recordings were made from anteroventral third ventricle (AV3V) and supraoptic nucleus (SON) neurons of rat hypothalamus in slice preparations. ET-3 was applied at concentrations of 10(-10) to 3 x 10(-7) M. Of 119 AV3V neurons tested, 21 (18%) were excited, 8 (6%) were slightly inhibited, and 90 (76%) were unaffected. The threshold concentration to evoke responses was approximately 10(-8) M. Excitatory responses of the AV3V neurons to ET-3 remained in a Ca(2+)-free medium. Of 120 SON neurons tested, 46 were phasic (putative vasopressin neuron) and 74 were nonphasic (putative oxytocin neuron). Of 46 phasic neurons tested, 26 (56.5%) were inhibited by ET-3, 20 (43.5%) were nonresponsive, and none was excited. Of 74 nonphasic neurons tested, 14 (19%) neurons were inhibited by ET-3, 60 (81%) were nonresponsive, and none was excited. These results suggest that ET-3 has dual effects on AV3V and SON neurons and the mechanisms of the responses may be different in the AV3V and SON neurons.
在脑片标本中,从大鼠下丘脑的腹前第三脑室(AV3V)和视上核(SON)神经元进行细胞外记录。以10(-10)至3×10(-7)M的浓度应用ET-3。在119个被测试的AV3V神经元中,21个(18%)被兴奋,8个(6%)受到轻微抑制,90个(76%)未受影响。诱发反应的阈值浓度约为10(-8)M。AV3V神经元对ET-3的兴奋反应在无钙培养基中依然存在。在120个被测试的SON神经元中,46个为相位性(推测为血管加压素神经元),74个为非相位性(推测为催产素神经元)。在46个被测试的相位性神经元中,26个(56.5%)被ET-3抑制,20个(43.5%)无反应,无一个被兴奋。在74个被测试的非相位性神经元中,14个(19%)被ET-3抑制,60个(81%)无反应,无一个被兴奋。这些结果表明,ET-3对AV3V和SON神经元具有双重作用,且在AV3V和SON神经元中的反应机制可能不同。