• 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

相似文献

1
Intranasally administered neuropeptide S (NPS) exerts anxiolytic effects following internalization into NPS receptor-expressing neurons.经鼻内给予神经肽 S(NPS)后,可通过内化到表达 NPS 受体的神经元中发挥抗焦虑作用。
Neuropsychopharmacology. 2012 May;37(6):1323-37. doi: 10.1038/npp.2011.317. Epub 2012 Jan 25.
2
Identification of a role for the ventral hippocampus in neuropeptide S-elicited anxiolysis.腹侧海马在神经肽 S 引起的焦虑缓解中的作用鉴定。
PLoS One. 2013;8(3):e60219. doi: 10.1371/journal.pone.0060219. Epub 2013 Mar 28.
3
Nasal application of neuropeptide S reduces anxiety and prolongs memory in rats: social versus non-social effects.鼻内应用神经肽 S 可减少大鼠的焦虑并延长记忆:社交与非社交效应。
Neuropharmacology. 2012 Jan;62(1):398-405. doi: 10.1016/j.neuropharm.2011.08.016. Epub 2011 Aug 18.
4
Neuropeptide S alters anxiety, but not depression-like behaviour in Flinders Sensitive Line rats: a genetic animal model of depression.神经肽 S 改变焦虑,但不改变抑郁样行为的弗林德斯敏感大鼠:一种遗传性抑郁动物模型。
Int J Neuropsychopharmacol. 2012 Apr;15(3):375-87. doi: 10.1017/S1461145711000678. Epub 2011 May 9.
5
Further studies on the pharmacological profile of the neuropeptide S receptor antagonist SHA 68.进一步研究神经肽 S 受体拮抗剂 SHA 68 的药理学特性。
Peptides. 2010 May;31(5):915-25. doi: 10.1016/j.peptides.2010.02.012. Epub 2010 Feb 19.
6
Neuropeptide S: a neuropeptide promoting arousal and anxiolytic-like effects.神经肽S:一种促进觉醒和抗焦虑样作用的神经肽。
Neuron. 2004 Aug 19;43(4):487-97. doi: 10.1016/j.neuron.2004.08.005.
7
Neuropeptide S reduces mouse aggressiveness in the resident/intruder test through selective activation of the neuropeptide S receptor.神经肽S通过选择性激活神经肽S受体降低小鼠在定居者/入侵者测试中的攻击性。
Neuropharmacology. 2015 Oct;97:1-6. doi: 10.1016/j.neuropharm.2015.05.002. Epub 2015 May 13.
8
The ventromedial hypothalamic nucleus plays an important role in anxiolytic-like effect of neuropeptide S.室旁下丘脑核在神经肽 S 的抗焦虑样作用中发挥重要作用。
Neuropeptides. 2018 Feb;67:36-44. doi: 10.1016/j.npep.2017.11.004. Epub 2017 Nov 7.
9
Anxiolytic- and panicolytic-like effects of Neuropeptide S in the mouse elevated T-maze.神经肽 S 在小鼠高架 T 迷宫中产生的抗焦虑和恐慌样作用。
Eur J Neurosci. 2012 Dec;36(11):3531-7. doi: 10.1111/j.1460-9568.2012.08265.x. Epub 2012 Aug 29.
10
Pharmacology of neuropeptide S in mice: therapeutic relevance to anxiety disorders.小鼠中神经肽S的药理学:与焦虑症的治疗相关性。
Psychopharmacology (Berl). 2008 May;197(4):601-11. doi: 10.1007/s00213-008-1080-4. Epub 2008 Mar 3.

引用本文的文献

1
Peroxisome proliferator-activated receptor-α activation facilitates contextual fear extinction and modulates intrinsic excitability of dentate gyrus neurons.过氧化物酶体增殖物激活受体-α 的激活促进情境性恐惧的消退,并调节齿状回神经元的内在兴奋性。
Transl Psychiatry. 2023 Jun 15;13(1):206. doi: 10.1038/s41398-023-02496-1.
2
Hippocampus: Molecular, Cellular, and Circuit Features in Anxiety.海马:焦虑症的分子、细胞和回路特征。
Neurosci Bull. 2023 Jun;39(6):1009-1026. doi: 10.1007/s12264-023-01020-1. Epub 2023 Jan 21.
3
Chronic treatment with escitalopram and venlafaxine affects the neuropeptide S pathway differently in adult Wistar rats exposed to maternal separation.在经历母体分离的成年Wistar大鼠中,艾司西酞普兰和文拉法辛的长期治疗对神经肽S通路的影响不同。
AIMS Neurosci. 2022 Sep 13;9(3):395-422. doi: 10.3934/Neuroscience.2022022. eCollection 2022.
4
A Role for Neuropeptide S in Alcohol and Cocaine Seeking.神经肽S在觅酒和觅可卡因行为中的作用。
Pharmaceuticals (Basel). 2022 Jun 27;15(7):800. doi: 10.3390/ph15070800.
5
Relationship of Neuropeptide S with Clinical and Metabolic Parameters of Patients during Rehabilitation Therapy for Schizophrenia.精神分裂症康复治疗期间神经肽S与患者临床及代谢参数的关系
Brain Sci. 2022 Jun 11;12(6):768. doi: 10.3390/brainsci12060768.
6
Can Neuropeptide S Be an Indicator for Assessing Anxiety in Psychiatric Disorders?神经肽 S 能否成为评估精神障碍焦虑的指标?
Front Public Health. 2022 Apr 26;10:872430. doi: 10.3389/fpubh.2022.872430. eCollection 2022.
7
Protein-Protein Interaction Network Analysis Revealed a New Prospective of Posttraumatic Stress Disorder.蛋白质-蛋白质相互作用网络分析揭示了创伤后应激障碍的新前景。
Galen Med J. 2018 May 29;7:e1137. doi: 10.22086/gmj.v0i0.1137. eCollection 2018.
8
Role of the Neuropeptide S System in Emotionality, Stress Responsiveness and Addiction-Like Behaviours in Rodents: Relevance to Stress-Related Disorders.神经肽S系统在啮齿动物情绪、应激反应及成瘾样行为中的作用:与应激相关疾病的关联
Pharmaceuticals (Basel). 2021 Aug 8;14(8):780. doi: 10.3390/ph14080780.
9
Neuropeptide S Receptor as an Innovative Therapeutic Target for Parkinson Disease.神经肽S受体作为帕金森病的创新治疗靶点
Pharmaceuticals (Basel). 2021 Aug 6;14(8):775. doi: 10.3390/ph14080775.
10
Dissociative Effects of Neuropeptide S Receptor Deficiency and Nasal Neuropeptide S Administration on T-Maze Discrimination and Reversal Learning.神经肽S受体缺乏及经鼻给予神经肽S对T迷宫辨别和逆向学习的分离效应
Pharmaceuticals (Basel). 2021 Jul 5;14(7):643. doi: 10.3390/ph14070643.

本文引用的文献

1
Tumor suppressor down-regulated in renal cell carcinoma 1 (DRR1) is a stress-induced actin bundling factor that modulates synaptic efficacy and cognition.抑瘤基因下调在肾细胞癌 1(DRR1)中是一种应激诱导的肌动蛋白成束因子,调节突触效能和认知。
Proc Natl Acad Sci U S A. 2011 Oct 11;108(41):17213-8. doi: 10.1073/pnas.1103318108. Epub 2011 Oct 3.
2
Attenuation of cocaine-induced conditioned locomotion is associated with altered expression of hippocampal glutamate receptors in mice lacking LPA1 receptors.缺乏 LPA1 受体的小鼠中海马谷氨酸受体表达改变与可卡因诱导的条件性运动减弱有关。
Psychopharmacology (Berl). 2012 Mar;220(1):27-42. doi: 10.1007/s00213-011-2446-6. Epub 2011 Sep 2.
3
Synthesis and separation of the enantiomers of the neuropeptide S receptor antagonist (9R/S)-3-oxo-1,1-diphenyl-tetrahydro-oxazolo[3,4-a]pyrazine-7-carboxylic acid 4-fluoro-benzylamide (SHA 68).神经肽 S 受体拮抗剂(9R/S)-3-氧代-1,1-二苯基-四氢-恶唑并[3,4-a]吡嗪-7-羧酸 4-氟苄基酰胺(SHA 68)的对映异构体的合成与分离。
J Med Chem. 2011 Apr 28;54(8):2738-44. doi: 10.1021/jm200138r. Epub 2011 Apr 5.
4
Intraventricular administration of neuropeptide S has reward-like effects.脑室给药神经肽 S 具有奖赏样效应。
Eur J Pharmacol. 2011 May 1;658(1):16-21. doi: 10.1016/j.ejphar.2011.02.009. Epub 2011 Feb 22.
5
Neuropeptide S enhances memory during the consolidation phase and interacts with noradrenergic systems in the brain.神经肽 S 可增强巩固阶段的记忆,并与大脑中的去甲肾上腺素能系统相互作用。
Neuropsychopharmacology. 2011 Mar;36(4):744-52. doi: 10.1038/npp.2010.207. Epub 2010 Dec 8.
6
Immunohistochemical localization of the neuropeptide S receptor in the rat central nervous system.神经肽 S 受体在大鼠中枢神经系统中的免疫组织化学定位。
Neuroscience. 2011 Jan 13;172:153-63. doi: 10.1016/j.neuroscience.2010.10.020. Epub 2010 Oct 13.
7
CBT for pharmacotherapy non-remitters--a systematic review of a next-step strategy.药物治疗无缓解者的认知行为治疗-下一步策略的系统评价。
J Affect Disord. 2011 Mar;129(1-3):219-28. doi: 10.1016/j.jad.2010.08.025. Epub 2010 Sep 21.
8
Neuropeptide S stimulates dopaminergic neurotransmission in the medial prefrontal cortex.神经肽 S 刺激前额皮质内侧的多巴胺能神经传递。
J Neurochem. 2010 Oct;115(2):475-82. doi: 10.1111/j.1471-4159.2010.06947.x. Epub 2010 Aug 30.
9
Neuropeptide S receptor gene -- converging evidence for a role in panic disorder.神经肽 S 受体基因——惊恐障碍发病机制中的作用证据不断汇集。
Mol Psychiatry. 2011 Sep;16(9):938-48. doi: 10.1038/mp.2010.81. Epub 2010 Jul 6.
10
Intranasal administration of nerve growth factor produces antidepressant-like effects in animals.鼻腔内给予神经生长因子可在动物中产生抗抑郁样作用。
Neurochem Res. 2010 Sep;35(9):1302-14. doi: 10.1007/s11064-010-0183-6. Epub 2010 Jun 3.

经鼻内给予神经肽 S(NPS)后,可通过内化到表达 NPS 受体的神经元中发挥抗焦虑作用。

Intranasally administered neuropeptide S (NPS) exerts anxiolytic effects following internalization into NPS receptor-expressing neurons.

机构信息

Max Planck Institute of Psychiatry, Munich, Germany.

出版信息

Neuropsychopharmacology. 2012 May;37(6):1323-37. doi: 10.1038/npp.2011.317. Epub 2012 Jan 25.

DOI:10.1038/npp.2011.317
PMID:22278093
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3327839/
Abstract

Experiments in rodents revealed neuropeptide S (NPS) to constitute a potential novel treatment option for anxiety diseases such as panic and post-traumatic stress disorder. However, both its cerebral target sites and the molecular underpinnings of NPS-mediated effects still remain elusive. By administration of fluorophore-conjugated NPS, we pinpointed NPS target neurons in distinct regions throughout the entire brain. We demonstrated their functional relevance in the hippocampus. In the CA1 region, NPS modulates synaptic transmission and plasticity. NPS is taken up into NPS receptor-expressing neurons by internalization of the receptor-ligand complex as we confirmed by subsequent cell culture studies. Furthermore, we tracked internalization of intranasally applied NPS at the single-neuron level and additionally demonstrate that it is delivered into the mouse brain without losing its anxiolytic properties. Finally, we show that NPS differentially modulates the expression of proteins of the glutamatergic system involved inter alia in synaptic plasticity. These results not only enlighten the path of NPS in the brain, but also establish a non-invasive method for NPS administration in mice, thus strongly encouraging translation into a novel therapeutic approach for pathological anxiety in humans.

摘要

在啮齿类动物实验中发现,神经肽 S(NPS)可能成为治疗焦虑症(如恐慌症和创伤后应激障碍)的新方法。然而,其脑内靶标和 NPS 介导作用的分子基础仍然难以捉摸。通过给予荧光标记的 NPS,我们确定了整个大脑中不同区域 NPS 的靶神经元。我们在海马体中证明了它们的功能相关性。在 CA1 区域,NPS 调节突触传递和可塑性。我们通过后续的细胞培养研究证实,NPS 通过受体-配体复合物的内化被摄取到表达 NPS 受体的神经元中。此外,我们在单细胞水平上追踪了经鼻内给予的 NPS 的内化,并进一步证明它可以进入小鼠大脑而不会失去其抗焦虑特性。最后,我们表明 NPS 可调节谷氨酸能系统蛋白的表达,这些蛋白参与突触可塑性等过程。这些结果不仅阐明了 NPS 在大脑中的途径,还建立了一种在小鼠中给予 NPS 的非侵入性方法,因此强烈鼓励将其转化为治疗病理性焦虑的新方法。