Yang Z, Bertram D, Coote J H
Department of Physiology, The Medical School, The University of Birmingham, B15 2TT, Birmingham, UK.
Brain Res. 2001 Jul 20;908(1):99-103. doi: 10.1016/s0006-8993(01)02593-8.
Neurones in the paraventricular nucleus of the hypothalamus project to rostral ventrolateral medullary spinally projecting vasomotor neurones. We studied the excitatory action and the role of glutamate and vasopressin in this pathway in anaesthetised rats. A five barrel micropipette assembly was used for extracellular recording of neuronal activity and for microiontophoresis of drugs into the vicinity of identified medullary vasomotor neurones. Iontophoresis of L-glutamate or vasopressin into the vicinity of a vasomotor neurone increased activity, effects which were blocked by simultaneous iontophoretic application of a glutamate receptor antagonist, or a vasopressin V(1a) antagonist respectively. Paraventricular neurones were activated either by microinjecting D,L-homocysteic acid or by disinhibition by microinjecting bicuculline. The excitatory effects on vasomotor neurones, of paraventricular nucleus stimulation at some sites were prevented by simultaneous microiontophoretic application of kynurenic acid or at other sites by application of V(1a) antagonist. Neither antagonist altered the ongoing activity of the vasomotor neurones. Therefore, glutamate or vasopressin may act as excitatory neurotransmitters at synapses of paraventricular neurones on rostral ventrolateral medullary vasomotor neurones.
下丘脑室旁核中的神经元投射至延髓头端腹外侧的脊髓投射性血管运动神经元。我们研究了谷氨酸和血管加压素在此通路中对麻醉大鼠的兴奋作用及其作用机制。使用五管微量移液器组件对神经元活动进行细胞外记录,并将药物微量离子导入已识别的延髓血管运动神经元附近。将L-谷氨酸或血管加压素微量离子导入血管运动神经元附近会增加其活动,这些作用分别被同时微量离子导入谷氨酸受体拮抗剂或血管加压素V(1a)拮抗剂所阻断。通过微量注射D,L-高半胱氨酸或微量注射荷包牡丹碱解除抑制来激活室旁神经元。在某些部位,通过同时微量离子导入犬尿氨酸可阻止室旁核刺激对血管运动神经元的兴奋作用,而在其他部位则通过应用V(1a)拮抗剂来阻止。两种拮抗剂均未改变血管运动神经元的持续活动。因此,谷氨酸或血管加压素可能在室旁神经元与延髓头端腹外侧血管运动神经元的突触处作为兴奋性神经递质起作用。