Vasopressin increases GABAergic inhibition of rat hypothalamic paraventricular nucleus neurons in vitro

被引:67
作者
Hermes, MLHJ
Ruijter, JM
Klop, A
Buijs, RM
Renaud, LP
机构
[1] Netherlands Inst Brain Res, NL-1105 AZ Amsterdam, Netherlands
[2] Ottawa Civic Hosp, Loeb Res Inst, Ottawa, ON K1Y 4E9, Canada
[3] Univ Ottawa, Ottawa, ON K1Y 4E9, Canada
[4] Univ Amsterdam, Acad Med Ctr, Dept Anat & Embryol, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1152/jn.2000.83.2.705
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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 redound 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.
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收藏
页码:705 / 711
页数:7
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