Noradrenaline activates vasopressin neurons via alpha(1)-receptor-mediated Ca2+ signaling pathway

被引:24
作者
Shioda, S
Yada, T
Muroya, S
Takigawa, M
Nakai, Y
机构
[1] KAGOSHIMA UNIV,SCH MED,DEPT PHYSIOL,KAGOSHIMA 890,JAPAN
[2] KAGOSHIMA UNIV,SCH MED,DEPT PSYCHIAT,KAGOSHIMA 890,JAPAN
[3] INST PHYSIOL SCI,LAB INTRACELLULAR METAB,OKAZAKI,AICHI 444,JAPAN
关键词
noradrenaline; alpha-adrenoceptor; vasopressin; cytosolic Ca2+; in vitro study; rat; cAMP; PARAVENTRICULAR NEUROSECRETORY NEURONS; RAT SUPRAOPTIC NUCLEUS; INVITRO; STIMULATION; CELLS; NOREPINEPHRINE; RELEASE;
D O I
10.1016/S0304-3940(97)00275-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Noradrenaline (Nn) (1-10 mu M), dibutyryl-cAMP (1-5 mM), and forskolin (10-20 mu M) increased cytosolic Ca2+ concentration ([Ca2+](i)) in isolated arginine-vasopressin (AVP)-containing neurons in the hypothalamic supraoptic nucleus (SON). The NA-induced increase in [Ca2+](i) in AVP-containing neurons was abolished by a specific alpha(1)-antagonist, prazosin (1 mu M) and was markedly reduced when treated with a protein kinase A (PKA) blocker, H89 (40 mu M). The NA-induced [Ca2+](i) was not altered by a protein kinase C (PKC) inhibitor, calphostin C (0.1 mu M) and a PKC activator, TPA (100 nM). In general, NA, a known neurotransmitter the SON, activates AVP-containing neurons via alpha(1)-receptor which is linked to stimulation of cAMP-PKA-regulated Ca2+ signaling pathway. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:210 / 212
页数:3
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