Hermes M L, Ruijter J M, Klop A, Buijs R M, Renaud L P
Netherlands Institute for Brain Research, 1105 AZ Amsterdam, The Netherlands.
J Neurophysiol. 2000 Feb;83(2):705-11. doi: 10.1152/jn.2000.83.2.705.
This investigation used an in vitro hypothalamic brain slice preparation and whole cell and perforated-patch recording to examine the response of magnocellular neurons in hypothalamic paraventricular nucleus (PVN) to bath applications of vasopressin (VP; 100-500 nM). In 22/38 cells, responses were characterized by an increase in the frequency of bicuculline-sensitive inhibitory postsynaptic potentials or currents with no detectable influence on excitatory postsynaptic events. Perforated-patch recordings confirmed that VP did not have an effect on intrinsic membrane properties of magnocellular PVN neurons (n = 17). Analysis of intrinsic membrane properties obtained with perforated-patch recording (n = 23) demonstrated that all of nine VP-sensitive neurons showed a rebound depolarization after transient membrane hyperpolarization from rest. By contrast, 12/14 nonresponding neurons displayed a delayed return to resting membrane potentials. Recordings of reversed inhibitory postsynaptic currents with chloride-loaded electrodes showed that responses to VP persisted in media containing glutamate receptor antagonists but were abolished in the presence of tetrodotoxin. In addition, responses were mimicked by vasotocin [Phe(2), Orn(8)], a selective V(1a) receptor agonist, and blocked by [beta-Mercapto-beta, beta-cyclopentamethylenepropionyl(1),O-Me-Tyr(2), Arg(8)]-VP (Manning compound), a V(1a)/OT receptor antagonist. Neither [deamino-Cys(1),Val(4),D-Arg(8)]-VP, a selective V(2) receptor agonist, nor oxytocin were effective. Collectively, the results imply that VP acts at V(1a) receptors to excite GABAergic neurons that are presynaptic to a population of magnocellular PVN neurons the identity of which features a unique rebound depolarization. Endogenous sources of VP may be VP-synthesizing neurons in suprachiasmatic nucleus, known to project toward the perinuclear regions of PVN, and/or the magnocellular neurons within PVN.
本研究采用体外下丘脑脑片制备技术以及全细胞和穿孔膜片钳记录方法,来检测下丘脑室旁核(PVN)大细胞神经元对浴槽中应用血管加压素(VP;100 - 500 nM)的反应。在38个细胞中的22个细胞中,反应表现为荷包牡丹碱敏感的抑制性突触后电位或电流频率增加,而对兴奋性突触后事件无明显影响。穿孔膜片钳记录证实,VP对PVN大细胞神经元的内在膜特性没有影响(n = 17)。对穿孔膜片钳记录获得的内在膜特性进行分析(n = 23)表明,9个对VP敏感的神经元在从静息状态短暂膜超极化后均表现出反弹去极化。相比之下,14个无反应的神经元中有12个表现出延迟恢复到静息膜电位。用氯化物负载电极记录反向抑制性突触后电流表明,对VP的反应在含有谷氨酸受体拮抗剂的培养基中持续存在,但在河豚毒素存在时被消除。此外,血管紧张素[Phe(2), Orn(8)](一种选择性V(1a)受体激动剂)可模拟该反应,而V(1a)/OT受体拮抗剂[β-巯基-β,β-环戊亚甲基丙酰(1),O-甲基-Tyr(2), Arg(8)]-VP(曼宁化合物)可阻断该反应。选择性V(2)受体激动剂[脱氨基-Cys(1),Val(4),D-Arg(8)]-VP和催产素均无效。总体而言,结果表明VP作用于V(1a)受体,以兴奋一群PVN大细胞神经元突触前的GABA能神经元,这群神经元的特征是具有独特的反弹去极化。VP的内源性来源可能是视交叉上核中合成VP的神经元,已知其投射至PVN的核周区域,和/或PVN内的大细胞神经元。