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神经肽Y抑制大鼠垂体前叶细胞分泌催乳素:通过抑制钙内流与多巴胺相互作用的证据。

Neuropeptide Y suppresses prolactin secretion from rat anterior pituitary cells: evidence for interactions with dopamine through inhibitory coupling to calcium entry.

作者信息

Wang J, Ciofi P, Crowley W R

机构信息

Department of Pharmacology, University of Tennessee, Memphis College of Medicine 38163, USA.

出版信息

Endocrinology. 1996 Feb;137(2):587-94. doi: 10.1210/endo.137.2.8593806.

Abstract

Expression of neuropeptide Y (NPY) in the medial basal hypothalamus is increased during lactation, and at least part of this increase is due to the appearance of the peptide in hypothalamic tuberoinfundibular dopamine neurons, a cell population that does not exhibit NPY expression in other physiological conditions. The present studies tested the hypothesis that NPY affects PRL secretion by modulating the action of dopamine (DA) at the lactotroph. In static incubations of cultured anterior pituitary (AP) cells, the addition of either NPY or DA in concentrations of 0.1-500 nM resulted in dose-dependent inhibition of PRL secretion, and the combination of DA and NPY in submaximal concentrations produced an additive inhibition of PRL release. NPY also inhibited PRL secretion induced by TRH in perifused AP cells, and the effects were again additive with DA. The interactions of NPY and DA on TRH-induced elevations in cytosolic Ca2+ ([Ca2+]i) were examined by loading cultured AP cells of lactating rats with the fluorescent calcium probe fura-2 TRH produced a dose-dependent stimulation of [Ca2+]i, which was characterized by a rapid transient spike and a more prolonged plateau. Both phases were attenuated by either DA or NPY at 100 nM and were nearly abolished by the combination of DA and NPY, whereas neither DA nor NPY altered resting [Ca2+]i. DA and NPY also inhibited the increases in PRL secretion and [Ca2+]i induced by elevated extracellular K+ in an additive manner. Stimulation of AP cells with TRH in the absence of extracellular Ca2+ resulted in an attenuated spike of PRL release and [Ca2+]i and no plateau phase. Under these conditions, DA still inhibited the residual [Ca2+]i and PRL responses, but the inhibitory effects of NPY on PRL secretion and [Ca2+]i, and the potentiation by NPY of DA inhibition, were abolished. These results suggest that one physiological function of the NPY expressed in tuberoinfundibular dopamine neurons in lactation is to amplify the inhibitory action of DA on PRL secretion through negative coupling to the Ca2+ messenger system, particularly the entry of extracellular Ca2+.

摘要

哺乳期内侧基底下丘脑神经肽Y(NPY)的表达增加,且这种增加至少部分归因于该肽在下丘脑结节漏斗多巴胺神经元中的出现,而在其他生理条件下该细胞群体不表达NPY。本研究检验了NPY通过调节多巴胺(DA)对催乳素细胞的作用来影响催乳素分泌的假说。在培养的垂体前叶(AP)细胞的静态孵育中,添加浓度为0.1 - 500 nM的NPY或DA均可导致催乳素分泌呈剂量依赖性抑制,且亚最大浓度的DA和NPY联合使用对催乳素释放产生相加性抑制。NPY还抑制了在灌流的AP细胞中由促甲状腺激素释放激素(TRH)诱导的催乳素分泌,其作用与DA再次呈现相加性。通过用荧光钙探针fura - 2加载哺乳期大鼠的培养AP细胞,研究了NPY和DA对TRH诱导的胞质Ca2 +([Ca2 +]i)升高的相互作用。TRH产生了[Ca2 +]i的剂量依赖性刺激,其特征为快速的瞬时峰值和更持久的平台期。在100 nM时,DA或NPY均使这两个阶段减弱,而DA和NPY联合使用则几乎完全消除这两个阶段,而DA和NPY均未改变静息[Ca2 +]i。DA和NPY还以相加的方式抑制了细胞外K +升高诱导的催乳素分泌和[Ca2 +]i的增加。在无细胞外Ca2 +的情况下用TRH刺激AP细胞导致催乳素释放和[Ca2 +]i的峰值减弱且无平台期。在这些条件下,DA仍抑制残余的[Ca2 +]i和催乳素反应,但NPY对催乳素分泌和[Ca2 +]i的抑制作用以及NPY对DA抑制的增强作用均被消除。这些结果表明,哺乳期结节漏斗多巴胺神经元中表达的NPY的一种生理功能是通过与Ca2 +信使系统负偶联,特别是细胞外Ca2 +的内流,来放大DA对催乳素分泌的抑制作用。

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