• 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

分布于整个新皮层的长程GABA能连接及其可能的功能。

Long-Range GABAergic Connections Distributed throughout the Neocortex and their Possible Function.

作者信息

Tamamaki Nobuaki, Tomioka Ryohei

机构信息

Department of Morphological Neural Science, Graduate School of Medical Sciences, Kumamoto University Kumamoto, Japan.

出版信息

Front Neurosci. 2010 Dec 8;4:202. doi: 10.3389/fnins.2010.00202. eCollection 2010.

DOI:10.3389/fnins.2010.00202
PMID:21151790
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3000116/
Abstract

Features and functions of long-range GABAergic projection neurons in the developing cerebral cortex have been reported previously, although until now their significance in the adult cerebral cortex has remained uncertain. The septo-hippocampal circuit is one exception - in this system, long-range mature GABAergic projection neurons have been well analyzed and their contribution to the generation of theta-oscillatory behavior in the hippocampus has been documented. To have a clue to the function of the GABAergic projection neurons in the neocortex, we view how the long-range GABAergic projections are integrated in the cortico-cortical, cortico-fugal, and afferent projections in the cerebral cortex. Then, we consider the possibility that the GABAergic projection neurons are involved in the generation, modification, and/or synchronization of oscillations in mature neocortical neuron activity. When markers that identify the GABAergic projection neurons are examined in anatomical and developmental studies, it is clear that neuronal NO synthetase (nNOS)-immunoreactivity can readily identify GABAergic projection neurons. GABAergic projection neurons account for 0.5% of the neocortical GABAergic neurons. To elucidate the role of the GABAergic projection neurons in the neocortex, it will be necessary to clarify the network constructed by nNOS-positive GABAergic projection neurons and their postsynaptic targets. Thus, our long-range goals will be to label and manipulate (including deleting) the GABAergic projection neurons using genetic tools driven by a nNOS promoter. We recognize that this may be a complex endeavor, as most excitatory neurons in the murine neocortex express nNOS transiently. Nevertheless, additional studies characterizing long-range GABAergic projection neurons will have great value to the overall understanding of mature cortical function.

摘要

发育中的大脑皮质中长距离GABA能投射神经元的特征和功能此前已有报道,尽管迄今为止它们在成人大脑皮质中的意义仍不明确。隔区-海马回路是一个例外——在这个系统中,长距离成熟GABA能投射神经元已得到充分分析,并且它们对海马体中θ振荡行为产生的贡献也已被记录。为了了解新皮质中GABA能投射神经元的功能,我们观察了长距离GABA能投射是如何整合到大脑皮质的皮质-皮质、皮质-传出和传入投射中的。然后,我们考虑了GABA能投射神经元参与成熟新皮质神经元活动振荡的产生、调节和/或同步的可能性。当在解剖学和发育研究中检查识别GABA能投射神经元的标记物时,很明显神经元型一氧化氮合酶(nNOS)免疫反应性能够轻易识别GABA能投射神经元。GABA能投射神经元占新皮质GABA能神经元的0.5%。为了阐明GABA能投射神经元在新皮质中的作用,有必要弄清楚由nNOS阳性GABA能投射神经元及其突触后靶点构建的网络。因此,我们的长期目标是利用由nNOS启动子驱动的基因工具标记和操纵(包括删除)GABA能投射神经元。我们认识到这可能是一项复杂的工作,因为小鼠新皮质中的大多数兴奋性神经元会短暂表达nNOS。尽管如此,对长距离GABA能投射神经元进行的更多特征研究将对全面理解成熟皮质功能具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b01/3000116/6c8b7892910a/fnins-04-00202-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b01/3000116/6dc49e7d108c/fnins-04-00202-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b01/3000116/3df506a07cb1/fnins-04-00202-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b01/3000116/681e94e88ec4/fnins-04-00202-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b01/3000116/6c8b7892910a/fnins-04-00202-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b01/3000116/6dc49e7d108c/fnins-04-00202-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b01/3000116/3df506a07cb1/fnins-04-00202-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b01/3000116/681e94e88ec4/fnins-04-00202-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b01/3000116/6c8b7892910a/fnins-04-00202-g004.jpg

相似文献

1
Long-Range GABAergic Connections Distributed throughout the Neocortex and their Possible Function.分布于整个新皮层的长程GABA能连接及其可能的功能。
Front Neurosci. 2010 Dec 8;4:202. doi: 10.3389/fnins.2010.00202. eCollection 2010.
2
Long-range GABAergic projection neurons in the cat neocortex.猫新皮层中的长距离γ-氨基丁酸能投射神经元。
J Comp Neurol. 2007 Jul 20;503(3):421-31. doi: 10.1002/cne.21395.
3
Demonstration of long-range GABAergic connections distributed throughout the mouse neocortex.分布于整个小鼠新皮层的长距离γ-氨基丁酸能连接的证明。
Eur J Neurosci. 2005 Mar;21(6):1587-600. doi: 10.1111/j.1460-9568.2005.03989.x.
4
Subtypes of GABAergic neurons project axons in the neocortex.GABA 能神经元的亚型投射轴突到新皮层。
Front Neuroanat. 2009 Nov 9;3:25. doi: 10.3389/neuro.05.025.2009. eCollection 2009.
5
Long-Range GABAergic Projections of Cortical Origin in Brain Function.大脑功能中源自皮质的长距离γ-氨基丁酸能投射
Front Syst Neurosci. 2022 Mar 22;16:841869. doi: 10.3389/fnsys.2022.841869. eCollection 2022.
6
A Non-Canonical Cortico-Amygdala Inhibitory Loop.非经典的皮质-杏仁核抑制环路。
J Neurosci. 2019 Oct 23;39(43):8424-8438. doi: 10.1523/JNEUROSCI.1515-19.2019. Epub 2019 Sep 11.
7
Corticofugal GABAergic projection neurons in the mouse frontal cortex.小鼠额叶皮质中的皮质下行GABA能投射神经元。
Front Neuroanat. 2015 Oct 28;9:133. doi: 10.3389/fnana.2015.00133. eCollection 2015.
8
Structural organization of long-range GABAergic projection system of the hippocampus.海马长程 GABA 能投射系统的结构组织。
Front Neuroanat. 2009 Jul 20;3:13. doi: 10.3389/neuro.05.013.2009. eCollection 2009.
9
The origin of neocortical nitric oxide synthase-expressing inhibitory neurons.新皮层表达一氧化氮合酶的抑制性神经元的起源。
Front Neural Circuits. 2012 Jul 9;6:44. doi: 10.3389/fncir.2012.00044. eCollection 2012.
10
Mature astrocytes transform into transitional radial glia within adult mouse neocortex that supports directed migration of transplanted immature neurons.成熟星形胶质细胞在成年小鼠新皮质内转变为过渡性放射状胶质细胞,后者支持移植的未成熟神经元的定向迁移。
Exp Neurol. 1999 May;157(1):43-57. doi: 10.1006/exnr.1999.6982.

引用本文的文献

1
GABAergic dysfunction in postmortem dorsolateral prefrontal cortex: implications for cognitive deficits in schizophrenia and affective disorders.死后背外侧前额叶皮质中的γ-氨基丁酸能功能障碍:对精神分裂症和情感障碍认知缺陷的影响
Front Cell Neurosci. 2024 Sep 24;18:1440834. doi: 10.3389/fncel.2024.1440834. eCollection 2024.
2
Long-range inhibition from prelimbic to cingulate areas of the medial prefrontal cortex enhances network activity and response execution.前额皮质内额前皮质的边缘抑制到扣带区域增强了网络活动和反应执行。
Nat Commun. 2024 Jul 10;15(1):5772. doi: 10.1038/s41467-024-50055-z.
3
Paraventricular Hypothalamic Nucleus Upregulates Intraocular Pressure Via Glutamatergic Neurons.

本文引用的文献

1
A novel in vivo inducible dendritic cell ablation model in mice.一种新型的小鼠体内可诱导树突状细胞消融模型。
Biochem Biophys Res Commun. 2010 Jul 2;397(3):559-63. doi: 10.1016/j.bbrc.2010.05.157.
2
The subplate and early cortical circuits.基板和早期皮质回路。
Annu Rev Neurosci. 2010;33:23-48. doi: 10.1146/annurev-neuro-060909-153244.
3
Abnormal neural oscillations and synchrony in schizophrenia.精神分裂症中的异常神经振荡和同步。
室旁下丘脑核通过谷氨酸能神经元上调眼内压。
Invest Ophthalmol Vis Sci. 2023 Sep 1;64(12):43. doi: 10.1167/iovs.64.12.43.
4
Localization and Diagnostic Specificity of Glutamic Acid Decarboxylase Transcript Alterations in the Dorsolateral Prefrontal Cortex in Schizophrenia.谷氨酸脱羧酶转录本在精神分裂症患者外侧前额叶皮质中的定位和诊断特异性。
Biol Psychiatry. 2023 Aug 15;94(4):322-331. doi: 10.1016/j.biopsych.2023.04.003. Epub 2023 Apr 14.
5
New insights into binocular rivalry from the reconstruction of evolving percepts using model network dynamics.利用模型网络动力学对不断演变的感知进行重建,从而获得对双眼竞争的新见解。
Front Comput Neurosci. 2023 Mar 24;17:1137015. doi: 10.3389/fncom.2023.1137015. eCollection 2023.
6
Prefrontal Interneurons: Populations, Pathways, and Plasticity Supporting Typical and Disordered Cognition in Rodent Models.前额叶中间神经元:支持啮齿动物模型中典型和异常认知的种群、通路和可塑性。
J Neurosci. 2022 Nov 9;42(45):8468-8476. doi: 10.1523/JNEUROSCI.1136-22.2022.
7
The Distinct Characteristics of Somatostatin Neurons in the Human Brain.人脑生长抑素神经元的独特特征。
Mol Neurobiol. 2022 Aug;59(8):4953-4965. doi: 10.1007/s12035-022-02892-6. Epub 2022 Jun 4.
8
Top-down control of hippocampal signal-to-noise by prefrontal long-range inhibition.前额叶长程抑制对海马信号噪声比的自上而下控制。
Cell. 2022 Apr 28;185(9):1602-1617.e17. doi: 10.1016/j.cell.2022.04.001.
9
Long-Range GABAergic Projections of Cortical Origin in Brain Function.大脑功能中源自皮质的长距离γ-氨基丁酸能投射
Front Syst Neurosci. 2022 Mar 22;16:841869. doi: 10.3389/fnsys.2022.841869. eCollection 2022.
10
VIP-Expressing GABAergic Neurons: Disinhibitory vs. Inhibitory Motif and Its Role in Communication Across Neocortical Areas.表达血管活性肠肽的γ-氨基丁酸能神经元:去抑制与抑制模式及其在跨新皮质区域通讯中的作用
Front Cell Neurosci. 2022 Feb 10;16:811484. doi: 10.3389/fncel.2022.811484. eCollection 2022.
Nat Rev Neurosci. 2010 Feb;11(2):100-13. doi: 10.1038/nrn2774.
4
Control of hippocampal gamma oscillation frequency by tonic inhibition and excitation of interneurons.通过中间神经元的紧张性抑制和兴奋来控制海马γ振荡频率。
Nat Neurosci. 2010 Feb;13(2):205-12. doi: 10.1038/nn.2464. Epub 2009 Dec 20.
5
Two separate subtypes of early non-subplate projection neurons in the developing cerebral cortex of rodents.两种在啮齿类动物大脑皮质发育过程中独立的早期非基板投射神经元亚型。
Front Neuroanat. 2009 Nov 17;3:27. doi: 10.3389/neuro.05.027.2009. eCollection 2009.
6
Subtypes of GABAergic neurons project axons in the neocortex.GABA 能神经元的亚型投射轴突到新皮层。
Front Neuroanat. 2009 Nov 9;3:25. doi: 10.3389/neuro.05.025.2009. eCollection 2009.
7
Structural organization of long-range GABAergic projection system of the hippocampus.海马长程 GABA 能投射系统的结构组织。
Front Neuroanat. 2009 Jul 20;3:13. doi: 10.3389/neuro.05.013.2009. eCollection 2009.
8
Parvalbumin neurons and gamma rhythms enhance cortical circuit performance.小白蛋白神经元和γ节律增强皮层回路性能。
Nature. 2009 Jun 4;459(7247):698-702. doi: 10.1038/nature07991. Epub 2009 Apr 26.
9
Driving fast-spiking cells induces gamma rhythm and controls sensory responses.驱动快速发放细胞可诱导γ节律并控制感觉反应。
Nature. 2009 Jun 4;459(7247):663-7. doi: 10.1038/nature08002. Epub 2009 Apr 26.
10
Characterization of engineered channelrhodopsin variants with improved properties and kinetics.具有改进特性和动力学的工程化视紫红质通道变体的表征。
Biophys J. 2009 Mar 4;96(5):1803-14. doi: 10.1016/j.bpj.2008.11.034.