• 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

可兴奋神经元的神经调节。

Neuronomodulation of Excitable Neurons.

机构信息

Institute of Neuroscience, Second Military Medical University, Shanghai, 200433, China.

Institute for Brain Research and Rehabilitation, Key Laboratory of Brain, Cognition and Education Sciences of Ministry of Education, South China Normal University, Guangzhou, 510631, China.

出版信息

Neurosci Bull. 2024 Jan;40(1):103-112. doi: 10.1007/s12264-023-01095-w. Epub 2023 Aug 16.

DOI:10.1007/s12264-023-01095-w
Abstract

Neuronomodulation refers to the modulation of neural conduction and synaptic transmission (i.e., the conduction process involved in synaptic transmission) of excitable neurons via changes in the membrane potential in response to chemical substances, from spillover neurotransmitters to paracrine or endocrine hormones circulating in the blood. Neuronomodulation can be direct or indirect, depending on the transduction pathways from the ligand binding site to the ion pore, either on the same molecule, i.e. the ion channel, or through an intermediate step on different molecules. The major players in direct neuronomodulation are ligand-gated or voltage-gated ion channels. The key process of direct neuronomodulation is the binding and chemoactivation of ligand-gated or voltage-gated ion channels, either orthosterically or allosterically, by various ligands. Indirect neuronomodulation involves metabotropic receptor-mediated slow potentials, where steroid hormones, cytokines, and chemokines can implement these actions. Elucidating neuronomodulation is of great significance for understanding the physiological mechanisms of brain function, and the occurrence and treatment of diseases.

摘要

神经调节是指通过改变膜电位对化学物质(包括从溢出的神经递质到在血液中循环的旁分泌或内分泌激素)的反应,来调节可兴奋神经元的神经传导和突触传递(即突触传递所涉及的传导过程)。神经调节可以是直接的,也可以是间接的,这取决于从配体结合位点到离子通道的转导途径,是在同一分子(即离子通道)上,还是通过不同分子的中间步骤。直接神经调节的主要参与者是配体门控或电压门控离子通道。直接神经调节的关键过程是各种配体对离子通道的正位或变构结合和化学激活,包括配体门控和电压门控离子通道。间接神经调节涉及代谢型受体介导的缓慢电位,甾体激素、细胞因子和趋化因子可以通过这些作用来实现。阐明神经调节对于理解大脑功能的生理机制以及疾病的发生和治疗具有重要意义。

相似文献

1
Neuronomodulation of Excitable Neurons.可兴奋神经元的神经调节。
Neurosci Bull. 2024 Jan;40(1):103-112. doi: 10.1007/s12264-023-01095-w. Epub 2023 Aug 16.
2
Regulation of ion channel expression in neural cells by hormones and growth factors.激素和生长因子对神经细胞中离子通道表达的调节。
Mol Neurobiol. 1998 Dec;18(3):175-225. doi: 10.1007/BF02741300.
3
Ligand-gated ion channels in the enteric nervous system.肠神经系统中的配体门控离子通道。
Neurogastroenterol Motil. 2002 Dec;14(6):611-23. doi: 10.1046/j.1365-2982.2002.00363.x.
4
Neuronal excitability: voltage-dependent currents and synaptic transmission.神经元兴奋性:电压依赖性电流与突触传递。
J Clin Neurophysiol. 1992 Apr;9(2):195-211.
5
Zinc and copper influence excitability of rat olfactory bulb neurons by multiple mechanisms.锌和铜通过多种机制影响大鼠嗅球神经元的兴奋性。
J Neurophysiol. 2001 Oct;86(4):1652-60. doi: 10.1152/jn.2001.86.4.1652.
6
Effects of mercurials on ligand- and voltage-gated ion channels: a review.汞剂对配体门控和电压门控离子通道的影响:综述
Neurotoxicology. 1996 Spring;17(1):63-84.
7
The contribution of ion channels in input-output plasticity.离子通道在输入-输出可塑性中的作用。
Neurobiol Learn Mem. 2019 Dec;166:107095. doi: 10.1016/j.nlm.2019.107095. Epub 2019 Sep 17.
8
Calcium Signalling through Ligand-Gated Ion Channels such as P2X1 Receptors in the Platelet and other Non-Excitable Cells.通过配体门控离子通道(如血小板和其他非可兴奋细胞中的P2X1受体)进行的钙信号传导。
Adv Exp Med Biol. 2016;898:305-29. doi: 10.1007/978-3-319-26974-0_13.
9
Sigma-1 Receptor and Neuronal Excitability.西格玛-1受体与神经元兴奋性
Handb Exp Pharmacol. 2017;244:109-130. doi: 10.1007/164_2017_8.
10
Structural determinants of voltage-gating properties in calcium channels.钙通道电压门控特性的结构决定因素。
Elife. 2021 Mar 30;10:e64087. doi: 10.7554/eLife.64087.

引用本文的文献

1
Genetics-Based Targeting Strategies for Precise Neuromodulation.基于遗传学的精确神经调节靶向策略。
Adv Sci (Weinh). 2025 Jul;12(28):e13817. doi: 10.1002/advs.202413817. Epub 2025 May 19.
2
Progresses in Questing for the Truth of Opioid-Related Constipation in Cancer Patients.探索癌症患者阿片类药物相关性便秘真相的进展
J Cell Mol Med. 2025 Apr;29(8):e70553. doi: 10.1111/jcmm.70553.
3
The Chemokine CCL2 Promotes Excitatory Synaptic Transmission in Hippocampal Neurons via GluA1 Subunit Trafficking.趋化因子 CCL2 通过 GluA1 亚基转运促进海马神经元中的兴奋性突触传递。

本文引用的文献

1
Unique Pharmacology, Brain Dysfunction, and Therapeutic Advancements for Fentanyl Misuse and Abuse.芬太尼滥用和成瘾的独特药理学、大脑功能障碍和治疗进展。
Neurosci Bull. 2022 Nov;38(11):1365-1382. doi: 10.1007/s12264-022-00872-3. Epub 2022 May 15.
2
GABA receptors: structure, function, pharmacology, and related disorders.γ-氨基丁酸受体:结构、功能、药理学及相关疾病
J Genet Eng Biotechnol. 2021 Aug 21;19(1):123. doi: 10.1186/s43141-021-00224-0.
3
Structures of the glucocorticoid-bound adhesion receptor GPR97-G complex.糖皮质激素结合黏附受体 GPR97-G 复合物的结构。
Neurosci Bull. 2024 Nov;40(11):1649-1666. doi: 10.1007/s12264-024-01236-9. Epub 2024 Jul 2.
Nature. 2021 Jan;589(7843):620-626. doi: 10.1038/s41586-020-03083-w. Epub 2021 Jan 6.
4
Tumor Necrosis Factor α and Interleukin-1β Acutely Inhibit AgRP Neurons in the Arcuate Nucleus of the Hypothalamus.肿瘤坏死因子-α和白细胞介素-1β急性抑制下丘脑弓状核的 AgRP 神经元。
Int J Mol Sci. 2020 Nov 25;21(23):8928. doi: 10.3390/ijms21238928.
5
Hydrophobic Drug/Toxin Binding Sites in Voltage-Dependent K and Na Channels.电压依赖性钾通道和钠通道中的疏水性药物/毒素结合位点
Front Pharmacol. 2020 May 15;11:735. doi: 10.3389/fphar.2020.00735. eCollection 2020.
6
Structure-Function and Therapeutic Potential of Spider Venom-Derived Cysteine Knot Peptides Targeting Sodium Channels.靶向钠通道的蜘蛛毒液来源的半胱氨酸结肽的结构-功能及治疗潜力
Front Pharmacol. 2019 Apr 11;10:366. doi: 10.3389/fphar.2019.00366. eCollection 2019.
7
Gq-Coupled Muscarinic Receptor Enhancement of KCNQ2/3 Channels and Activation of TRPC Channels in Multimodal Control of Excitability in Dentate Gyrus Granule Cells.Gq 偶联毒蕈碱型乙酰胆碱受体增强 KCNQ2/3 通道和 TRPC 通道活性在齿状回颗粒细胞兴奋的多模态调控中的作用。
J Neurosci. 2019 Feb 27;39(9):1566-1587. doi: 10.1523/JNEUROSCI.1781-18.2018. Epub 2018 Dec 28.
8
The tarantula toxin GxTx detains K channel gating charges in their resting conformation.狼蛛毒素 GxTx 将 K 通道门控电荷固定在其静息构象。
J Gen Physiol. 2019 Mar 4;151(3):292-315. doi: 10.1085/jgp.201812213. Epub 2018 Nov 5.
9
Direct neurotransmitter activation of voltage-gated potassium channels.直接神经递质激活电压门控钾通道。
Nat Commun. 2018 May 10;9(1):1847. doi: 10.1038/s41467-018-04266-w.
10
Intense Activity of the Raphe Spinal Pathway Depresses Motor Activity via a Serotonin Dependent Mechanism.中缝脊髓束的强烈活动通过 5-羟色胺依赖机制抑制运动活动。
Front Neural Circuits. 2018 Jan 9;11:111. doi: 10.3389/fncir.2017.00111. eCollection 2017.