• 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

脑啡肽终末在大鼠蓝斑核中投射至内侧前额叶皮质的神经元上形成抑制性突触。

Enkephalin terminals form inhibitory-type synapses on neurons in the rat nucleus locus coeruleus that project to the medial prefrontal cortex.

作者信息

van Bockstaele E J, Colago E E, Pickel V M

机构信息

Department of Neurology and Neuroscience, Cornell University Medical College, New York, NY 10021, USA.

出版信息

Neuroscience. 1996 Mar;71(2):429-42. doi: 10.1016/0306-4522(95)00432-7.

DOI:10.1016/0306-4522(95)00432-7
PMID:9053798
Abstract

Norepinephrine-containing fibres in the medial prefrontal cortex derive from the locus coeruleus, a brainstem nucleus which also receives a dense innervation of enkephalin-immunoreactive axon terminals. We combined immunogold-silver labelling of retrogradely transported FluoroGold from the medial prefrontal cortex with immunoperoxidase detection of leucine5-enkephalin in the same section of tissue through the locus coeruleus of adult rats. This dual-labelling experiment was conducted to determine whether axon terminals containing lecuine5-enkephalin target neurons in the locus coeruleus that project to the frontal cortex and, if so, what are their morphological characteristics. By light microscopy, enkephalin-labelled processes overlapped FluoroGold retrogradely labelled neurons in the locus coeruleus. By electron microscopy, retrogradely labelled perikarya and dendrites were commonly enveloped by astrocytic processes and received few afferents in the plane of section examined. However, at sites unoccupied by glial processes, abundant afferent input could be identified. In addition, some FluoroGold-labelled perikarya and dendrites lacked this glial ensheathment but were more frequently apposed by axon terminals. Of 163 FluoroGold-labelled perikarya and dendrites examined where enkephalin immunoreactivity was present in the neuropil, 42% were contacted by enkephalin-immunoreactive axon terminals. The peroxidase-labelled enkephalin terminals as well as the unlabelled terminals often contained both small, clear and large dense core vesicles. Both labelled and unlabelled terminals also formed primary symmetric synapses characteristic of inhibitory transmitters with retrogradely labelled perikarya and proximal dendrites. At times, more than one enkephalin-labelled terminal was found to converge on a common retrogradely labelled perikarya or dendrite. These results demonstrate cellular sites where enkephalin-containing afferents may directly modulate and most likely inhibit the activity of cortically projecting neurons in the locus coeruleus.

摘要

内侧前额叶皮质中含去甲肾上腺素的纤维源自蓝斑,蓝斑是一个脑干核团,它也接受脑啡肽免疫反应性轴突终末的密集神经支配。我们将从内侧前额叶皮质逆行转运的荧光金的免疫金银标记与通过成年大鼠蓝斑在同一组织切片中对亮氨酸脑啡肽的免疫过氧化物酶检测相结合。进行这个双重标记实验是为了确定含有亮氨酸脑啡肽的轴突终末是否靶向投射到额叶皮质的蓝斑中的神经元,如果是,它们的形态特征是什么。通过光学显微镜观察,脑啡肽标记的突起与蓝斑中逆行标记的荧光金神经元重叠。通过电子显微镜观察,逆行标记的胞体和树突通常被星形胶质细胞突起包裹,并且在所检查的切片平面中接受的传入纤维很少。然而,在未被胶质细胞突起占据的部位,可以识别出丰富的传入输入。此外,一些荧光金标记的胞体和树突缺乏这种胶质细胞的包被,但更频繁地与轴突终末相邻。在163个荧光金标记的胞体和树突中,在神经毡中存在脑啡肽免疫反应性,其中42%与脑啡肽免疫反应性轴突终末接触。过氧化物酶标记的脑啡肽终末以及未标记的终末通常都含有小而清亮的囊泡和大的致密核心囊泡。标记和未标记的终末也都与逆行标记的胞体和近端树突形成了抑制性递质特有的初级对称突触。有时,发现不止一个脑啡肽标记的终末汇聚在一个共同的逆行标记的胞体或树突上。这些结果表明了含脑啡肽的传入纤维可能直接调节并最有可能抑制蓝斑中投射到皮质的神经元活动的细胞位点。

相似文献

1
Enkephalin terminals form inhibitory-type synapses on neurons in the rat nucleus locus coeruleus that project to the medial prefrontal cortex.脑啡肽终末在大鼠蓝斑核中投射至内侧前额叶皮质的神经元上形成抑制性突触。
Neuroscience. 1996 Mar;71(2):429-42. doi: 10.1016/0306-4522(95)00432-7.
2
Morphologically heterogeneous met-enkephalin terminals form synapses with tyrosine hydroxylase-containing dendrites in the rat nucleus locus coeruleus.形态学上异质性的甲硫氨酸脑啡肽终末与大鼠蓝斑核中含酪氨酸羟化酶的树突形成突触。
J Comp Neurol. 1995 Dec 18;363(3):423-38. doi: 10.1002/cne.903630307.
3
Corticotropin-releasing factor-containing axon terminals synapse onto catecholamine dendrites and may presynaptically modulate other afferents in the rostral pole of the nucleus locus coeruleus in the rat brain.含有促肾上腺皮质激素释放因子的轴突终末与儿茶酚胺能树突形成突触,并可能在突触前调节大鼠脑海马蓝斑核头端的其他传入神经。
J Comp Neurol. 1996 Jan 15;364(3):523-534. doi: 10.1002/(SICI)1096-9861(19960115)364:3<523::AID-CNE10>3.0.CO;2-Q.
4
Electron microscopic evidence for coexistence of leucine5-enkephalin and gamma-aminobutyric acid in a subpopulation of axon terminals in the rat locus coeruleus region.大鼠蓝斑核区域轴突终末亚群中亮氨酸脑啡肽与γ-氨基丁酸共存的电镜证据。
Brain Res. 1997 Jan 23;746(1-2):171-82. doi: 10.1016/s0006-8993(96)01194-8.
5
Ultrastructural evidence for convergence of enkephalin and adrenaline-containing axon terminals on common targets and their presynaptic associations in the rat nucleus locus coeruleus.大鼠蓝斑核中脑啡肽和含肾上腺素轴突终末在共同靶点上汇聚及其突触前联系的超微结构证据。
Brain Res. 1996 Apr 29;718(1-2):61-75. doi: 10.1016/0006-8993(96)00004-2.
6
Input from central nucleus of the amygdala efferents to pericoerulear dendrites, some of which contain tyrosine hydroxylase immunoreactivity.来自杏仁核中央核传出纤维至蓝斑周树突的输入,其中一些含有酪氨酸羟化酶免疫反应性。
J Neurosci Res. 1996 Aug 1;45(3):289-302. doi: 10.1002/(SICI)1097-4547(19960801)45:3<289::AID-JNR11>3.0.CO;2-#.
7
Mu-opioid receptor is located on the plasma membrane of dendrites that receive asymmetric synapses from axon terminals containing leucine-enkephalin in the rat nucleus locus coeruleus.在大鼠蓝斑核中,μ-阿片受体位于树突的质膜上,这些树突接收来自含有亮氨酸脑啡肽的轴突终末的不对称突触。
J Comp Neurol. 1996 Dec 2;376(1):65-74. doi: 10.1002/(SICI)1096-9861(19961202)376:1<65::AID-CNE4>3.0.CO;2-M.
8
Relationship of Met-enkephalin-like immunoreactivity to vagal afferents and motor dendrites in the nucleus of the solitary tract: a light and electron microscopic dual labeling study.孤束核中脑啡肽样免疫反应性与迷走神经传入纤维和运动神经元树突的关系:光镜和电镜双重标记研究
Brain Res. 1991 Jun 7;550(2):298-312. doi: 10.1016/0006-8993(91)91332-u.
9
Synaptic structure and connectivity of serotonin terminals in the ventral tegmental area: potential sites for modulation of mesolimbic dopamine neurons.腹侧被盖区中5-羟色胺终端的突触结构与连接性:中脑边缘多巴胺能神经元的潜在调控位点。
Brain Res. 1994 Jun 6;647(2):307-22. doi: 10.1016/0006-8993(94)91330-7.
10
Evidence for coexistence of enkephalin and glutamate in axon terminals and cellular sites for functional interactions of their receptors in the rat locus coeruleus.在大鼠蓝斑中,脑啡肽和谷氨酸在轴突终末共存的证据以及它们受体功能相互作用的细胞位点。
J Comp Neurol. 2000 Jan 31;417(1):103-14. doi: 10.1002/(sici)1096-9861(20000131)417:1<103::aid-cne8>3.0.co;2-l.

引用本文的文献

1
Hypocretin1/orexinA-immunoreactive axons form few synaptic contacts on rat ventral tegmental area neurons that project to the medial prefrontal cortex.食欲素1/阿立新A免疫反应性轴突在投射至内侧前额叶皮质的大鼠腹侧被盖区神经元上形成的突触联系很少。
BMC Neurosci. 2014 Sep 7;15:105. doi: 10.1186/1471-2202-15-105.
2
Ultrastructural analysis of rat ventrolateral periaqueductal gray projections to the A5 cell group.大鼠腹外侧水管周围灰质投射到 A5 细胞群的超微结构分析。
Neuroscience. 2012 Nov 8;224:145-59. doi: 10.1016/j.neuroscience.2012.08.021. Epub 2012 Aug 20.
3
The locus coeruleus: A key nucleus where stress and opioids intersect to mediate vulnerability to opiate abuse.
蓝斑核:一个关键核团,应激和阿片类药物在此交汇,共同介导阿片类药物滥用易感性。
Brain Res. 2010 Feb 16;1314:162-74. doi: 10.1016/j.brainres.2009.09.036. Epub 2009 Sep 16.
4
Corticotropin-releasing hormone receptors in the medial prefrontal cortex regulate hypothalamic-pituitary-adrenal activity and anxiety-related behavior regardless of prior stress experience.内侧前额叶皮质中的促肾上腺皮质激素释放激素受体调节下丘脑-垂体-肾上腺活动及焦虑相关行为,而不受既往应激经历的影响。
Brain Res. 2007 Dec;1186:212-23. doi: 10.1016/j.brainres.2007.07.100. Epub 2007 Sep 19.
5
Ultrastructural evidence for co-localization of corticotropin-releasing factor receptor and mu-opioid receptor in the rat nucleus locus coeruleus.促肾上腺皮质激素释放因子受体与μ-阿片受体在大鼠蓝斑核中共定位的超微结构证据。
Neurosci Lett. 2007 Feb 21;413(3):216-21. doi: 10.1016/j.neulet.2006.11.069. Epub 2006 Dec 15.
6
Noradrenergic excitation and inhibition of GABAergic cell types in rat frontal cortex.去甲肾上腺素能对大鼠额叶皮质中γ-氨基丁酸能细胞类型的兴奋和抑制作用
J Neurosci. 1998 Sep 1;18(17):6963-76. doi: 10.1523/JNEUROSCI.18-17-06963.1998.