• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

阉割会降低布罗卡斜带区和视前区性二态核中编码谷氨酸脱羧酶的mRNA的单细胞水平。

Castration decreases single cell levels of mRNA encoding glutamic acid decarboxylase in the diagonal band of broca and the sexually dimorphic nucleus of the preoptic area.

作者信息

Sagrillo C A, Selmanoff M

机构信息

Department of Physiology, University of Maryland, School of Medicine, Baltimore 21201-1559, USA.

出版信息

J Neuroendocrinol. 1997 Sep;9(9):699-706. doi: 10.1046/j.1365-2826.1997.00630.x.

DOI:10.1046/j.1365-2826.1997.00630.x
PMID:9355037
Abstract

Using quantitative in situ hybridization histochemistry (ISHH), we determined the effect of castration on single cell levels of glutamic acid decarboxylase (GAD) mRNA in discrete hypothalamic regions of the male rat brain associated with the control of gonadotropin secretion. A 48-base oligodeoxynucleotide probe was used to detect with equal affinity the two isoforms of GAD message, GAD65 and GAD67. GAD message also was quantitated in a number of selected areas of the brain to contrast GAD gene expression amongst several populations of GABAergic neurons. Comparison of 11 brain regions demonstrated a 9.3-fold range in the quantity of single cell GAD mRNA with levels being highest in the amygdala and the diagonal band of Broca, moderate in the piriform cortex, caudate nucleus, substantia innominata, globus pallidus, cingulate cortex and medial septal nucleus, and lowest in the lateral septal nucleus and the medial preoptic nucleus (MPN). Castration markedly reduced single cell GAD mRNA levels in the DBB and the MPN, two discrete hypothalamic structures known to contain dendritic fields, cell bodies, and axons of GnRH neurons projecting to the median eminence. A striking finding was a dense core of steroid-sensitive GABAergic neurons within the MPN comprising the sexually dimorphic nucleus of the preoptic area (SDN-POA). Similar to the MPN as a whole, the amount of GAD mRNA expressed by cells in the SDN-POA of sham operated control rats was greater than in castrated animals. GAD mRNA levels were inversely related to serum LH titers, suggesting a role for these neurons in the mechanism controlling gonadal steroid negative feedback on LH secretion. This report provides the basis for future work to determine if GAD65, GAD67 or whether both isoforms are affected by gonadal steroid input.

摘要

我们运用定量原位杂交组织化学(ISHH)技术,确定了去势对雄性大鼠大脑中与促性腺激素分泌控制相关的离散下丘脑区域谷氨酸脱羧酶(GAD)mRNA单细胞水平的影响。使用一个48个碱基的寡脱氧核苷酸探针以同等亲和力检测GAD信息的两种同工型,即GAD65和GAD67。还对大脑的一些选定区域的GAD信息进行了定量,以对比若干GABA能神经元群体之间的GAD基因表达。对11个脑区的比较表明,单细胞GAD mRNA的量有9.3倍的差异范围,杏仁核和布罗卡斜带中的水平最高,梨状皮质、尾状核、无名质、苍白球、扣带回皮质和内侧隔核中的水平中等,而外侧隔核和内侧视前核(MPN)中的水平最低。去势显著降低了DBB和MPN中单细胞GAD mRNA水平,这两个离散的下丘脑结构已知含有投射到正中隆起的GnRH神经元的树突野、细胞体和轴突。一个惊人的发现是,MPN内有一个对类固醇敏感的GABA能神经元密集核心,其包含视前区性二态核(SDN-POA)。与整个MPN相似,假手术对照大鼠SDN-POA中的细胞表达的GAD mRNA量大于去势动物。GAD mRNA水平与血清LH滴度呈负相关,表明这些神经元在控制性腺类固醇对LH分泌的负反馈机制中起作用。本报告为未来确定GAD65、GAD67或两种同工型是否受性腺类固醇输入影响的研究工作提供了基础。

相似文献

1
Castration decreases single cell levels of mRNA encoding glutamic acid decarboxylase in the diagonal band of broca and the sexually dimorphic nucleus of the preoptic area.阉割会降低布罗卡斜带区和视前区性二态核中编码谷氨酸脱羧酶的mRNA的单细胞水平。
J Neuroendocrinol. 1997 Sep;9(9):699-706. doi: 10.1046/j.1365-2826.1997.00630.x.
2
GABAergic neuronal activity and mRNA levels for both forms of glutamic acid decarboxylase (GAD65 and GAD67) are reduced in the diagonal band of Broca during the afternoon of proestrus.在发情前期的下午,布罗卡斜带区的GABA能神经元活动以及两种形式的谷氨酸脱羧酶(GAD65和GAD67)的mRNA水平均降低。
Brain Res. 1996 Sep 9;733(1):46-55. doi: 10.1016/0006-8993(96)00532-x.
3
Sex differences in GABA turnover and glutamic acid decarboxylase (GAD(65) and GAD(67)) mRNA in the rat hypothalamus.大鼠下丘脑γ-氨基丁酸(GABA)代谢及谷氨酸脱羧酶(GAD65和GAD67)mRNA的性别差异
Brain Res. 2000 Sep 29;878(1-2):11-9. doi: 10.1016/s0006-8993(00)02648-2.
4
Progesterone suppression of glutamic acid decarboxylase (GAD67) mRNA levels in the preoptic area: correlation to the luteinizing hormone surge.孕酮对视前区谷氨酸脱羧酶(GAD67)mRNA水平的抑制作用:与促黄体生成素激增的相关性。
Neuroendocrinology. 1995 Dec;62(6):562-70. doi: 10.1159/000127064.
5
Regulation of glutamic acid decarboxylase 65 and 67 gene expression by ovarian steroids: identification of two functionally distinct populations of GABA neurones in the preoptic area.卵巢甾体激素对谷氨酸脱羧酶65和67基因表达的调控:视前区中两类功能不同的γ-氨基丁酸能神经元的鉴定。
J Neuroendocrinol. 2002 Apr;14(4):310-7. doi: 10.1046/j.1365-2826.2002.00780.x.
6
GABA interneurons in the rat medial frontal cortex: characterization by quantitative in situ hybridization of the glutamic acid decarboxylase (GAD67) mRNA.大鼠内侧额叶皮质中的GABA中间神经元:通过谷氨酸脱羧酶(GAD67)mRNA的定量原位杂交进行表征。
Brain Res. 1993 May 21;611(2):187-96. doi: 10.1016/0006-8993(93)90502-e.
7
Selective regulation of glutamic decarboxylase isoform 65, but not isoform 67, in the bed nucleus of the stria terminalis and the preoptic area of the ewe brain across the estrous cycle.在发情周期中,母羊大脑终纹床核和视前区对谷氨酸脱羧酶65亚型而非67亚型的选择性调节。
Endocrinology. 2002 Feb;143(2):544-50. doi: 10.1210/endo.143.2.8610.
8
Role of the progesterone receptor in restrained glutamic acid decarboxylase gene expression in the hypothalamus during the preovulatory luteinizing hormone surge.孕激素受体在排卵前促黄体生成素激增期间对下丘脑谷氨酸脱羧酶基因表达抑制中的作用。
Neuroendocrinology. 2002 Nov;76(5):283-9. doi: 10.1159/000066628.
9
Castration rapidly decreases hypothalamic gamma-aminobutyric acidergic neuronal activity in both male and female rats.去势会迅速降低雄性和雌性大鼠下丘脑γ-氨基丁酸能神经元的活性。
Brain Res. 2000 Sep 29;878(1-2):1-10. doi: 10.1016/s0006-8993(00)02600-7.
10
Prolactin- and testosterone-induced inhibition of LH secretion after orchidectomy: role of preoptic and tuberoinfundibular gamma-aminobutyric acidergic neurones.催乳素和睾酮对去势术后促黄体生成素分泌的抑制作用:视前区和结节漏斗γ-氨基丁酸能神经元的作用
J Endocrinol. 1994 Oct;143(1):165-74. doi: 10.1677/joe.0.1430165.

引用本文的文献

1
Sex differences in chronic pain-induced mental disorders: Mechanisms of cerebral circuitry.慢性疼痛诱发精神障碍中的性别差异:脑回路机制
Front Mol Neurosci. 2023 Feb 20;16:1102808. doi: 10.3389/fnmol.2023.1102808. eCollection 2023.
2
Neurotoxicity by synthetic androgen steroids: oxidative stress, apoptosis, and neuropathology: A review.合成雄激素类固醇的神经毒性:氧化应激、细胞凋亡与神经病理学:综述
Curr Neuropharmacol. 2015 Jan;13(1):132-45. doi: 10.2174/1570159X13666141210221434.
3
A lumpers versus splitters approach to sexual differentiation of the brain.
脑性别的块状与分裂方法。
Front Neuroendocrinol. 2011 Apr;32(2):114-23. doi: 10.1016/j.yfrne.2011.01.004. Epub 2011 Feb 4.
4
Sex difference and response to testosterone in gabaergic cells of the medial preoptic nucleus and ventral bed nuclei of the stria terminalis in gerbils.沙鼠内侧视前核和终纹床核腹侧部 GABA 能神经元的性别差异及对睾酮的反应。
Horm Behav. 2011 Apr;59(4):473-6. doi: 10.1016/j.yhbeh.2011.01.006. Epub 2011 Jan 31.
5
Altered GABAA receptor-mediated synaptic transmission disrupts the firing of gonadotropin-releasing hormone neurons in male mice under conditions that mimic steroid abuse.改变 GABAA 受体介导的突触传递会破坏模拟类固醇滥用条件下雄性小鼠促性腺激素释放激素神经元的放电。
J Neurosci. 2010 May 12;30(19):6497-506. doi: 10.1523/JNEUROSCI.5383-09.2010.
6
Influence of 17beta-estradiol and progesterone on GABAergic gene expression in the arcuate nucleus, amygdala and hippocampus of the rhesus macaque.17β-雌二醇和孕酮对恒河猴弓状核、杏仁核和海马 GABA 能基因表达的影响。
Brain Res. 2010 Jan 11;1307:28-42. doi: 10.1016/j.brainres.2009.10.011. Epub 2009 Oct 13.
7
Chronic exposure to anabolic androgenic steroids alters neuronal function in the mammalian forebrain via androgen receptor- and estrogen receptor-mediated mechanisms.长期接触合成代谢雄激素类固醇会通过雄激素受体和雌激素受体介导的机制改变哺乳动物前脑的神经元功能。
J Neurosci. 2009 Oct 7;29(40):12484-96. doi: 10.1523/JNEUROSCI.3108-09.2009.
8
Effects of chronic exposure to an anabolic androgenic steroid cocktail on alpha5-receptor-mediated GABAergic transmission and neural signaling in the forebrain of female mice.长期暴露于合成代谢雄激素类固醇混合物对雌性小鼠前脑α5受体介导的γ-氨基丁酸能传递和神经信号传导的影响。
Neuroscience. 2009 Jun 30;161(2):526-37. doi: 10.1016/j.neuroscience.2009.03.039. Epub 2009 Mar 24.