• 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

靶向中枢神经系统中G蛋白门控内向整流钾通道(GIRK通道)的治疗潜力

Therapeutic potential of targeting G protein-gated inwardly rectifying potassium (GIRK) channels in the central nervous system.

作者信息

Jeremic Danko, Sanchez-Rodriguez Irene, Jimenez-Diaz Lydia, Navarro-Lopez Juan D

机构信息

Neurophysiology & Behavior Laboratory, Regional Centre for Biomedical Research, School of Medicine of Ciudad Real, University of Castilla-La Mancha, Spain.

Neurophysiology & Behavior Laboratory, Regional Centre for Biomedical Research, School of Medicine of Ciudad Real, University of Castilla-La Mancha, Spain.

出版信息

Pharmacol Ther. 2021 Jul;223:107808. doi: 10.1016/j.pharmthera.2021.107808. Epub 2021 Jan 18.

DOI:10.1016/j.pharmthera.2021.107808
PMID:33476640
Abstract

G protein-gated inwardly rectifying potassium channels (Kir3/GirK) are important for maintaining resting membrane potential, cell excitability and inhibitory neurotransmission. Coupled to numerous G protein-coupled receptors (GPCRs), they mediate the effects of many neurotransmitters, neuromodulators and hormones contributing to the general homeostasis and particular synaptic plasticity processes, learning, memory and pain signaling. A growing number of behavioral and genetic studies suggest a critical role for the appropriate functioning of the central nervous system, as well as their involvement in many neurologic and psychiatric conditions, such as neurodegenerative diseases, mood disorders, attention deficit hyperactivity disorder, schizophrenia, epilepsy, alcoholism and drug addiction. Hence, GirK channels emerge as a very promising tool to be targeted in the current scenario where these conditions already are or will become a global public health problem. This review examines recent findings on the physiology, function, dysfunction, and pharmacology of GirK channels in the central nervous system and highlights the relevance of GirK channels as a worthful potential target to improve therapies for related diseases.

摘要

G蛋白门控内向整流钾通道(Kir3/GirK)对于维持静息膜电位、细胞兴奋性和抑制性神经传递至关重要。它们与众多G蛋白偶联受体(GPCR)偶联,介导许多神经递质、神经调质和激素的作用,有助于整体内环境稳定以及特定的突触可塑性过程、学习、记忆和疼痛信号传导。越来越多的行为和遗传学研究表明,其正常功能对中枢神经系统至关重要,且它们还参与许多神经和精神疾病,如神经退行性疾病、情绪障碍、注意力缺陷多动障碍、精神分裂症、癫痫、酗酒和药物成瘾。因此,在这些疾病已经或即将成为全球公共卫生问题的当前情况下,GirK通道成为一个非常有前景的靶向治疗工具。本综述探讨了中枢神经系统中GirK通道在生理学、功能、功能障碍和药理学方面的最新研究发现,并强调了GirK通道作为改善相关疾病治疗的有价值潜在靶点的相关性。

相似文献

1
Therapeutic potential of targeting G protein-gated inwardly rectifying potassium (GIRK) channels in the central nervous system.靶向中枢神经系统中G蛋白门控内向整流钾通道(GIRK通道)的治疗潜力
Pharmacol Ther. 2021 Jul;223:107808. doi: 10.1016/j.pharmthera.2021.107808. Epub 2021 Jan 18.
2
G-Protein-Gated Inwardly Rectifying Potassium (Kir3/GIRK) Channels Govern Synaptic Plasticity That Supports Hippocampal-Dependent Cognitive Functions in Male Mice.G 蛋白门控内向整流钾 (Kir3/GIRK) 通道调节支持雄性小鼠海马依赖认知功能的突触可塑性。
J Neurosci. 2021 Aug 18;41(33):7086-7102. doi: 10.1523/JNEUROSCI.2849-20.2021. Epub 2021 Jul 14.
3
New insights into the therapeutic potential of Girk channels.Girk 通道治疗潜力的新见解。
Trends Neurosci. 2014 Jan;37(1):20-9. doi: 10.1016/j.tins.2013.10.006. Epub 2013 Nov 21.
4
Emerging roles for G protein-gated inwardly rectifying potassium (GIRK) channels in health and disease.G 蛋白门控内向整流钾 (GIRK) 通道在健康和疾病中的新兴作用。
Nat Rev Neurosci. 2010 May;11(5):301-15. doi: 10.1038/nrn2834. Epub 2010 Apr 14.
5
GIRK Channel Plasticity and Implications for Drug Addiction.GIRK通道可塑性及其对药物成瘾的影响。
Int Rev Neurobiol. 2015;123:201-38. doi: 10.1016/bs.irn.2015.05.011. Epub 2015 Jun 22.
6
G Protein-Gated K Channel Ablation in Forebrain Pyramidal Neurons Selectively Impairs Fear Learning.前脑锥体神经元中G蛋白门控钾通道的消融选择性地损害恐惧学习。
Biol Psychiatry. 2016 Nov 15;80(10):796-806. doi: 10.1016/j.biopsych.2015.10.004. Epub 2015 Nov 10.
7
Inhibition of G-protein-activated inwardly rectifying K+ channels by the selective norepinephrine reuptake inhibitors atomoxetine and reboxetine.选择性去甲肾上腺素再摄取抑制剂托莫西汀和瑞波西汀抑制 G 蛋白激活内向整流钾通道。
Neuropsychopharmacology. 2010 Jun;35(7):1560-9. doi: 10.1038/npp.2010.27. Epub 2010 Mar 10.
8
[Roles of G Protein-gated Inward Rectifier Potassium Channels in Substance Addiction].[G蛋白偶联内向整流钾通道在物质成瘾中的作用]
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2020 Feb 28;42(1):108-116. doi: 10.3881/j.issn.1000-503X.10972.
9
Direct modulation of G protein-gated inwardly rectifying potassium (GIRK) channels.G蛋白门控内向整流钾通道(GIRK)的直接调控
Front Physiol. 2024 Jun 6;15:1386645. doi: 10.3389/fphys.2024.1386645. eCollection 2024.
10
G Protein-Gated Potassium Channels: A Link to Drug Addiction.G蛋白门控钾通道:与药物成瘾的联系。
Trends Pharmacol Sci. 2017 Apr;38(4):378-392. doi: 10.1016/j.tips.2017.01.007. Epub 2017 Feb 7.

引用本文的文献

1
Mechanistic correlation of potassium channel sensing and nitric oxide activity in neuroinflammation.神经炎症中钾通道传感与一氧化氮活性的机制关联
Mol Biol Rep. 2025 Sep 8;52(1):874. doi: 10.1007/s11033-025-10954-w.
2
Structural insights into the catalytic cycle of G protein-coupled receptor kinase 5 and a possible regulatory site for potassium ion.对G蛋白偶联受体激酶5催化循环的结构见解以及钾离子的一个可能调节位点。
J Biol Chem. 2025 May 29;301(7):110309. doi: 10.1016/j.jbc.2025.110309.
3
Further Structure-Activity Relationship of G Protein-Gated Inwardly Rectifying Potassium Channels 1/2 Activators: Synthesis and Biological Characterization of In Vitro Tool Compounds.
G蛋白门控内向整流钾通道1/2激活剂的进一步构效关系:体外工具化合物的合成与生物学特性
ChemMedChem. 2025 Jul 1;20(13):e202500037. doi: 10.1002/cmdc.202500037. Epub 2025 May 9.
4
Effects of Opioids in Cancer Pain: An Interplay Among Genetic Factors, Immune Response, and Clinical Outcomes-A Scoping Review.阿片类药物对癌症疼痛的影响:遗传因素、免疫反应与临床结局之间的相互作用——一项范围综述
Cancers (Basel). 2025 Mar 3;17(5):863. doi: 10.3390/cancers17050863.
5
Preclinical Insights into the Role of Kir4.1 in Chronic Pain and Depression: Mechanisms and Therapeutic Potential.Kir4.1在慢性疼痛和抑郁症中的作用的临床前见解:机制与治疗潜力
Biomolecules. 2025 Jan 23;15(2):165. doi: 10.3390/biom15020165.
6
An In Silico Investigation of the Pathogenic G151R G Protein-Gated Inwardly Rectifying K Channel 4 Variant to Identify Small Molecule Modulators.对致病性G151R G蛋白门控内向整流钾通道4变体进行计算机模拟研究以鉴定小分子调节剂。
Biology (Basel). 2024 Nov 29;13(12):992. doi: 10.3390/biology13120992.
7
Serotonin Inhibition of Claustrum Projection Neurons: Ionic Mechanism, Receptor Subtypes and Consequences for Claustrum Computation.血清素对屏状核投射神经元的抑制作用:离子机制、受体亚型及对屏状核计算的影响
Cells. 2024 Nov 29;13(23):1980. doi: 10.3390/cells13231980.
8
Potassium channels in depression: emerging roles and potential targets.抑郁症中的钾通道:新出现的作用和潜在靶点。
Cell Biosci. 2024 Nov 11;14(1):136. doi: 10.1186/s13578-024-01319-0.
9
G protein-gated inwardly rectifying K (GIRK/K3) channels: Molecular, cellular, and subcellular diversity.G蛋白门控内向整流钾(GIRK/K3)通道:分子、细胞及亚细胞层面的多样性
Histol Histopathol. 2025 May;40(5):597-620. doi: 10.14670/HH-18-822. Epub 2024 Sep 26.
10
The involvement of K channels in depression and pharmacological effects of antidepressants on these channels.钾通道与抑郁症的关系以及抗抑郁药对这些通道的药理作用。
Transl Psychiatry. 2024 Oct 2;14(1):411. doi: 10.1038/s41398-024-03069-6.