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雌激素受体在调节去卵巢雌性大鼠视上核和室旁核中 NADPH 黄递酶阳性细胞数量中的作用。

Role of oestrogen receptors on the modulation of NADPH-diaphorase-positive cell number in supraoptic and paraventricular nuclei of ovariectomised female rats.

机构信息

Department of Psychobiology, Universidad Nacional de Educación a Distancia, Madrid, Spain.

出版信息

J Neuroendocrinol. 2013 Mar;25(3):244-50. doi: 10.1111/j.1365-2826.2012.02387.x.

DOI:10.1111/j.1365-2826.2012.02387.x
PMID:22967140
Abstract

Modulation of the nitric oxide producing system (demonstrated via the NADPH-diaphorase histochemical reaction) by oestradiol has been established in several structures of the rat brain. The present study aimed to explore the possible regulation of NADPH-diaphorase activity by oestradiol in neurones of the supraoptic (SON) and paraventricular (PVN) nuclei and the role of oestrogen receptors (ERα and ERβ) in this regulation. Adult ovariectomised rats were divided into six groups and injected either with vehicle or a single dose of oestradiol, a selective ERα agonist-PPT [4,4',4″-(4-propyl-[1H]-pyrazole-1,3,5-triyl)trisphenol], a selective ERβ agonist-DPN [2,3-bis(4-hydroxyphenyl)-propionitrile], a selective ERα antagonist-MPP [1,3-bis(4-hydroxyphenyl)-4-methyl-5-[4-(2-piperidinylethoxy)phenol]-1H-pyrazole dihydrochloride] or a selective ERβ antagonist-PHTPP (4-[2-phenyl-5,7-bis(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-3-yl]phenol). The number of NADPH-diaphorase positive elements in the SON and the PVN was modulated by both ERs but, depending on the nucleus, ERα and ERβ ligands induced different effects. These results suggest that the regulation of nitrergic system by ERs may play a role in the control of oestrogen-dependent physiological mechanisms regulated by the SON and the PVN.

摘要

雌激素对大鼠脑内多种结构中一氧化氮产生系统(通过 NADPH 黄递酶组织化学反应证明)的调节作用已得到证实。本研究旨在探讨雌激素对神经细胞超神(SON)和室旁核(PVN)中 NADPH 黄递酶活性的可能调节作用,以及雌激素受体(ERα 和 ERβ)在这种调节中的作用。成年去卵巢大鼠分为六组,分别注射载体或单次剂量的雌激素、选择性 ERα 激动剂-PPT[4,4',4″-(4-丙基-[1H]-吡唑-1,3,5-三基)三苯酚]、选择性 ERβ 激动剂-DPN[2,3-双(4-羟苯基)-丙腈]、选择性 ERα 拮抗剂-MPP[1,3-双(4-羟苯基)-4-甲基-5-[4-(2-哌啶基乙氧基)苯酚]-1H-吡唑二盐酸盐]或选择性 ERβ 拮抗剂-PHTPP(4-[2-苯基-5,7-双(三氟甲基)吡唑并[1,5-a]嘧啶-3-基]苯酚)。SON 和 PVN 中的 NADPH 黄递酶阳性元素的数量受到 ERs 的调节,但取决于核,ERα 和 ERβ 配体诱导了不同的影响。这些结果表明,ERs 对氮能系统的调节可能在控制由 SON 和 PVN 调节的雌激素依赖性生理机制中发挥作用。

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