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本文引用的文献

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GABA(A) receptor alpha4 subunit suppression prevents withdrawal properties of an endogenous steroid.γ-氨基丁酸A型(GABA(A))受体α4亚基的抑制可防止内源性类固醇的戒断特性。
Nature. 1998 Apr 30;392(6679):926-30. doi: 10.1038/31948.
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Plasticity in fast synaptic inhibition of adult oxytocin neurons caused by switch in GABA(A) receptor subunit expression.成年催产素神经元快速突触抑制中的可塑性,由γ-氨基丁酸A(GABA(A))受体亚基表达的转换引起。
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Estrogen regulation of GABA transmission in rat preoptic area.雌激素对大鼠视前区γ-氨基丁酸传递的调节作用
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Sex and the developing brain: suppression of neuronal estrogen sensitivity by developmental androgen exposure.性别与发育中的大脑:发育过程中雄激素暴露对神经元雌激素敏感性的抑制作用。
Neurochem Res. 1997 Nov;22(11):1395-414. doi: 10.1023/a:1022027408234.
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Neuronally restricted RNA splicing regulates the expression of a novel GABAA receptor subunit conferring atypical functional properties [corrected; erratum to be published].神经元限制性RNA剪接调节一种具有非典型功能特性的新型GABAA受体亚基的表达[已修正;勘误将发表]
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Behavioral effects of 3 alpha-androstanediol. II: Hypothalamic and preoptic area actions via a GABAergic mechanism.
Behav Brain Res. 1996 Sep;79(1-2):119-30. doi: 10.1016/0166-4328(96)00005-8.
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Behavioral effects of 3 alpha-androstanediol. I: Modulation of sexual receptivity and promotion of GABA-stimulated chloride flux.3α-雄甾二醇的行为效应。I:对性接受能力的调节及对γ-氨基丁酸刺激的氯通量的促进作用。
Behav Brain Res. 1996 Sep;79(1-2):109-18. doi: 10.1016/0166-4328(96)00004-6.
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Inhibition of male sex behavior by androgen receptor blockade in preoptic area or hypothalamus, but not amygdala or septum.
Physiol Behav. 1996 Sep;60(3):783-9. doi: 10.1016/0031-9384(96)00088-1.
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GABAA receptor-mediated responses in the ventromedial nucleus of the hypothalamus of female and male neonatal rats.雌性和雄性新生大鼠下丘脑腹内侧核中GABAA受体介导的反应。
Neuroendocrinology. 1996 Aug;64(2):103-13. doi: 10.1159/000127105.
10
Plasticity in GABAA receptor subunit mRNA expression by hypothalamic magnocellular neurons in the adult rat.成年大鼠下丘脑大细胞神经元GABAA受体亚基mRNA表达的可塑性
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激素对大鼠脑性二态区GABAA受体γ亚基mRNA的依赖性调控

Hormone-dependent regulation of GABAA receptor gamma subunit mRNAs in sexually dimorphic regions of the rat brain.

作者信息

Clark A S, Myers M, Robinson S, Chang P, Henderson L P

机构信息

Department of Psychology, Dartmouth College, Hanover, NH 03755, USA.

出版信息

Proc Biol Sci. 1998 Oct 7;265(1408):1853-9. doi: 10.1098/rspb.1998.0512.

DOI:10.1098/rspb.1998.0512
PMID:9802242
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1689368/
Abstract

Transmission mediated by gamma-aminobutyric acid type A (GABAA) receptors expressed within the medial preoptic area (mPOA) and the ventromedial nucleus (VMN) of the hypothalamus is known to play critical, but contrasting, roles in regulating steroid-dependent sexual behaviours in rats. Previous studies have demonstrated a striking dichotomy in receptor composition between the two regions with regard to gamma, but not alpha or beta, subunit expression. To test if gonadal steroids regulate the expression of the gamma subunit genes within the mPOA and the VMN, in situ hybridization analysis for messenger RNAs encoding the gamma 1, gamma 2Short (gamma 2S) and gamma 2Long (gamma 2L) subunits was done in gonadectomized male and female rats and in gonadally intact females over the oestrous cycle. No significant differences in the expression of the gamma subunit mRNAs were observed in gonadectomized male versus female rats. Significant effects of gonadal state in female rats were observed for gamma 1 mRNA levels in the mPOA and gamma 2L levels in the VMN. These data demonstrate that gonadal hormones exert activational control of expression of GABAA receptor gamma subunit mRNAs and suggest that differences in receptor structure may contribute to the functional modulation of female sexual behaviours mediated by GABAergic transmission in these regions.

摘要

由下丘脑内侧视前区(mPOA)和腹内侧核(VMN)中表达的A型γ-氨基丁酸(GABAA)受体介导的传递,在调节大鼠类固醇依赖性性行为中发挥着关键但相反的作用。先前的研究表明,就γ亚基表达而言,这两个区域在受体组成上存在显著差异,而α或β亚基表达则无差异。为了测试性腺类固醇是否调节mPOA和VMN内γ亚基基因的表达,对去势的雄性和雌性大鼠以及处于发情周期的性腺完整雌性大鼠进行了原位杂交分析,以检测编码γ1、γ2短亚型(γ2S)和γ2长亚型(γ2L)亚基的信使RNA。在去势的雄性和雌性大鼠中,未观察到γ亚基mRNA表达的显著差异。在雌性大鼠中,观察到性腺状态对mPOA中γ1 mRNA水平和VMN中γ2L水平有显著影响。这些数据表明,性腺激素对GABAA受体γ亚基mRNA的表达具有激活调控作用,并表明受体结构的差异可能有助于这些区域中由GABA能传递介导的雌性性行为的功能调节。