• 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
Ciproxifan, an H3 receptor antagonist, alleviates hyperactivity and cognitive deficits in the APP Tg2576 mouse model of Alzheimer's disease.西普西凡,一种 H3 受体拮抗剂,可缓解阿尔茨海默病 APP Tg2576 小鼠模型的多动和认知缺陷。
Neurobiol Learn Mem. 2011 Jan;95(1):64-72. doi: 10.1016/j.nlm.2010.10.008. Epub 2010 Nov 10.
2
Histamine H3 Receptor Antagonist Prevents Memory Deficits and Synaptic Plasticity Disruption Following Isoflurane Exposure.组胺H3受体拮抗剂可预防异氟烷暴露后的记忆缺陷和突触可塑性破坏。
CNS Neurosci Ther. 2017 Apr;23(4):301-309. doi: 10.1111/cns.12675. Epub 2017 Feb 6.
3
Single dose of H3 receptor antagonist--ciproxifan--abolishes negative effects of chronic stress on cognitive processes in rats.单次给予 H3 受体拮抗剂——西普利他嗪——可消除慢性应激对大鼠认知过程的负面影响。
Psychopharmacology (Berl). 2014 Jan;231(1):209-19. doi: 10.1007/s00213-013-3227-1. Epub 2013 Aug 24.
4
Ryanodine receptor blockade reduces amyloid-β load and memory impairments in Tg2576 mouse model of Alzheimer disease.兰尼碱受体阻断剂可减少阿尔茨海默病 Tg2576 小鼠模型的淀粉样蛋白-β负荷和记忆障碍。
J Neurosci. 2012 Aug 22;32(34):11820-34. doi: 10.1523/JNEUROSCI.0875-12.2012.
5
Intermediate- and long-term recognition memory deficits in Tg2576 mice are reversed with acute calcineurin inhibition.Tg2576小鼠的中、长期认知记忆缺陷可通过急性抑制钙调神经磷酸酶得到逆转。
Behav Brain Res. 2009 Jun 8;200(1):95-9. doi: 10.1016/j.bbr.2008.12.034. Epub 2009 Jan 8.
6
Long-term (15 mo) dietary supplementation with pomegranates from Oman attenuates cognitive and behavioral deficits in a transgenic mice model of Alzheimer's disease.长期(15个月)补充来自阿曼的石榴可减轻阿尔茨海默病转基因小鼠模型的认知和行为缺陷。
Nutrition. 2015 Jan;31(1):223-9. doi: 10.1016/j.nut.2014.06.004. Epub 2014 Jun 25.
7
Chronic administration of R-flurbiprofen attenuates learning impairments in transgenic amyloid precursor protein mice.长期给予R-氟比洛芬可减轻转基因淀粉样前体蛋白小鼠的学习障碍。
BMC Neurosci. 2007 Jul 24;8:54. doi: 10.1186/1471-2202-8-54.
8
Ameliorative effects of yokukansan, a traditional Japanese medicine, on learning and non-cognitive disturbances in the Tg2576 mouse model of Alzheimer's disease.日本传统药物 yokukansan 对阿尔茨海默病 Tg2576 小鼠模型学习及非认知障碍的改善作用。
J Ethnopharmacol. 2009 Feb 25;122(1):157-62. doi: 10.1016/j.jep.2008.12.010. Epub 2008 Dec 25.
9
Impaired hippocampal acetylcholine release parallels spatial memory deficits in Tg2576 mice subjected to basal forebrain cholinergic degeneration.在基底前脑胆碱能退化的 Tg2576 小鼠中,海马乙酰胆碱释放受损与空间记忆缺陷平行。
Brain Res. 2014 Jan 16;1543:253-62. doi: 10.1016/j.brainres.2013.10.055. Epub 2013 Nov 11.
10
Ciproxifan improves cholinergic transmission, attenuates neuroinflammation and oxidative stress but does not reduce amyloid level in transgenic mice.环丙沙星可改善胆碱能传递,减轻神经炎症和氧化应激,但不会降低转基因小鼠的淀粉样蛋白水平。
Life Sci. 2017 Jul 1;180:23-35. doi: 10.1016/j.lfs.2017.05.013. Epub 2017 May 10.

引用本文的文献

1
Atrophy of hypothalamic subregions increases migraine risk: cross-sectional study and mendelian randomization analysis.下丘脑亚区域萎缩增加偏头痛风险:横断面研究与孟德尔随机化分析
J Headache Pain. 2025 Aug 6;26(1):178. doi: 10.1186/s10194-025-02119-8.
2
Early movement restriction impairs the development of sensorimotor integration, motor skills and memory in rats: Towards a preclinical model of developmental coordination disorder?早期运动限制会损害大鼠的感觉运动整合、运动技能和记忆发展:迈向发育协调障碍的临床前模型?
Eur J Neurosci. 2024 Dec;60(11):6830-6850. doi: 10.1111/ejn.16594. Epub 2024 Nov 10.
3
Targeting Microglia in Neuroinflammation: H3 Receptor Antagonists as a Novel Therapeutic Approach for Alzheimer's Disease, Parkinson's Disease, and Autism Spectrum Disorder.针对神经炎症中的小胶质细胞:H3受体拮抗剂作为阿尔茨海默病、帕金森病和自闭症谱系障碍的一种新型治疗方法。
Pharmaceuticals (Basel). 2024 Jun 25;17(7):831. doi: 10.3390/ph17070831.
4
Whole-brain mapping of histaminergic projections in mouse brain.在鼠脑内进行组胺能投射的全脑图谱绘制。
Proc Natl Acad Sci U S A. 2023 Apr 4;120(14):e2216231120. doi: 10.1073/pnas.2216231120. Epub 2023 Mar 28.
5
From attention-deficit hyperactivity disorder to sporadic Alzheimer's disease-Wnt/mTOR pathways hypothesis.从注意力缺陷多动障碍到散发性阿尔茨海默病——Wnt/mTOR通路假说
Front Neurosci. 2023 Feb 16;17:1104985. doi: 10.3389/fnins.2023.1104985. eCollection 2023.
6
Anti-inflammatory effects of new human histamine H receptor ligands with flavonoid structure on BV-2 neuroinflammation.具有黄酮结构的新型人组织胺 H 受体配体对 BV-2 神经炎症的抗炎作用。
Inflamm Res. 2023 Feb;72(2):181-194. doi: 10.1007/s00011-022-01658-z. Epub 2022 Nov 12.
7
The Novel Pimavanserin Derivative ST-2300 with Histamine H Receptor Affinity Shows Reduced 5-HT Binding, but Maintains Antidepressant- and Anxiolytic-like Properties in Mice.新型匹莫范色林衍生物 ST-2300 具有组胺 H 受体亲和力,与 5-HT 结合减少,但在小鼠中仍保持抗抑郁和抗焦虑样特性。
Biomolecules. 2022 May 10;12(5):683. doi: 10.3390/biom12050683.
8
Histamine H3 receptor antagonist, ciproxifan, alleviates cognition and synaptic plasticity alterations in a valproic acid-induced animal model of autism.组胺 H3 受体拮抗剂西普利他嗪可改善丙戊酸诱导的自闭症动物模型中的认知和突触可塑性改变。
Psychopharmacology (Berl). 2022 Aug;239(8):2673-2693. doi: 10.1007/s00213-022-06155-z. Epub 2022 May 11.
9
Chemical Probes for Histamine Receptor Subtypes.组胺受体亚型的化学探针
Curr Top Behav Neurosci. 2022;59:29-76. doi: 10.1007/7854_2021_254.
10
The Histaminergic System in Neuropsychiatric Disorders.神经精神疾病中的组胺能系统。
Biomolecules. 2021 Sep 11;11(9):1345. doi: 10.3390/biom11091345.

本文引用的文献

1
The H3 antagonist, ciproxifan, alleviates the memory impairment but enhances the motor effects of MK-801 (dizocilpine) in rats.H3 拮抗剂西普西芬可缓解 MK-801(地卓西平)引起的大鼠记忆障碍,但增强其运动效应。
Neuropharmacology. 2010 Nov;59(6):492-502. doi: 10.1016/j.neuropharm.2010.07.004. Epub 2010 Jul 16.
2
The H3 receptor antagonist clobenpropit protects against Abeta42-induced neurotoxicity in differentiated rat PC12 cells.H3受体拮抗剂氯苯丙哌嗪可保护分化的大鼠PC12细胞免受β淀粉样蛋白42诱导的神经毒性。
Pharmazie. 2010 Apr;65(4):257-60.
3
Intraneuronal beta-amyloid accumulation in the amygdala enhances fear and anxiety in Alzheimer's disease transgenic mice.杏仁核内的神经元β-淀粉样蛋白积累增强了阿尔茨海默病转基因小鼠的恐惧和焦虑。
Biol Psychiatry. 2010 Mar 15;67(6):513-21. doi: 10.1016/j.biopsych.2009.06.015. Epub 2009 Aug 7.
4
Effects of the H(3) antagonist, thioperamide, on behavioral alterations induced by systemic MK-801 administration in rats.H3拮抗剂硫代哌酰胺对大鼠全身给予MK-801所致行为改变的影响。
Psychopharmacology (Berl). 2009 Sep;205(4):589-97. doi: 10.1007/s00213-009-1566-8. Epub 2009 May 23.
5
Anxiolytic-like profiles of histamine H3 receptor agonists in animal models of anxiety: a comparative study with antidepressants and benzodiazepine anxiolytic.组胺H3受体激动剂在焦虑动物模型中的抗焦虑样作用:与抗抑郁药和苯二氮䓬类抗焦虑药的比较研究
Psychopharmacology (Berl). 2009 Aug;205(2):177-87. doi: 10.1007/s00213-009-1528-1. Epub 2009 Apr 9.
6
JNJ-10181457, a selective non-imidazole histamine H(3) receptor antagonist, normalizes acetylcholine neurotransmission and has efficacy in translational rat models of cognition.JNJ-10181457,一种选择性非咪唑类组胺H(3)受体拮抗剂,可使乙酰胆碱神经传递正常化,并在认知的转化大鼠模型中具有疗效。
Neuropharmacology. 2009 Jun;56(8):1131-7. doi: 10.1016/j.neuropharm.2009.03.011. Epub 2009 Apr 2.
7
Intermediate- and long-term recognition memory deficits in Tg2576 mice are reversed with acute calcineurin inhibition.Tg2576小鼠的中、长期认知记忆缺陷可通过急性抑制钙调神经磷酸酶得到逆转。
Behav Brain Res. 2009 Jun 8;200(1):95-9. doi: 10.1016/j.bbr.2008.12.034. Epub 2009 Jan 8.
8
Ameliorative effects of yokukansan, a traditional Japanese medicine, on learning and non-cognitive disturbances in the Tg2576 mouse model of Alzheimer's disease.日本传统药物 yokukansan 对阿尔茨海默病 Tg2576 小鼠模型学习及非认知障碍的改善作用。
J Ethnopharmacol. 2009 Feb 25;122(1):157-62. doi: 10.1016/j.jep.2008.12.010. Epub 2008 Dec 25.
9
Effects of the H3 receptor inverse agonist thioperamide on cocaine-induced locomotion in mice: role of the histaminergic system and potential pharmacokinetic interactions.H3受体反向激动剂硫代哌酰胺对可卡因诱导的小鼠运动的影响:组胺能系统的作用及潜在的药代动力学相互作用
Psychopharmacology (Berl). 2009 Mar;202(4):673-87. doi: 10.1007/s00213-008-1345-y. Epub 2008 Oct 9.
10
Preclinical investigations into the antipsychotic potential of the novel histamine H3 receptor antagonist GSK207040.新型组胺H3受体拮抗剂GSK207040抗精神病潜力的临床前研究。
Psychopharmacology (Berl). 2009 Jan;201(4):483-94. doi: 10.1007/s00213-008-1310-9. Epub 2008 Sep 3.

西普西凡,一种 H3 受体拮抗剂,可缓解阿尔茨海默病 APP Tg2576 小鼠模型的多动和认知缺陷。

Ciproxifan, an H3 receptor antagonist, alleviates hyperactivity and cognitive deficits in the APP Tg2576 mouse model of Alzheimer's disease.

机构信息

Department of Psychological Science, Northern Kentucky University, 1 Nunn Drive, Highland Heights, KY 41076, USA.

出版信息

Neurobiol Learn Mem. 2011 Jan;95(1):64-72. doi: 10.1016/j.nlm.2010.10.008. Epub 2010 Nov 10.

DOI:10.1016/j.nlm.2010.10.008
PMID:21073971
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3034295/
Abstract

Previous research has indicated that the blockade of H(3)-type histamine receptors may improve attention and memory in normal rodents. The purpose of this study was to determine if ciproxifan, an H(3) receptor antagonist, could alleviate the hyperactivity and cognitive deficits observed in a transgenic mouse model (APP(Tg2576)) of Alzheimer's disease. APP(Tg2576) mice displayed significantly greater locomotor activity than wild-type mice, but APP(Tg2576) mice provided with daily ciproxifan treatment showed activity levels that did not differ from wild-type mice. In the swim maze, APP(Tg2576) mice exhibited significantly longer escape latencies, but the APP(Tg2576) mice treated daily with ciproxifan had latencies that were indistinguishable from controls. In probe trials conducted one hour after the last training trial, ciproxifan-treated APP(Tg2576) mice spent more time near the previous platform location and made more crossings of this area than did saline-treated APP(Tg2576) mice. APP(Tg2576) mice also demonstrated a significant impairment in the object recognition task that was reversed by acute treatment with ciproxifan (3.0mg/kg). These data support the idea that modulation of H(3) receptors represents a novel and viable therapeutic strategy in the treatment of Alzheimer's disease.

摘要

先前的研究表明,阻断 H(3) 型组胺受体可能改善正常啮齿动物的注意力和记忆力。本研究的目的是确定 H(3) 受体拮抗剂西替利嗪是否能减轻阿尔茨海默病转基因小鼠模型(APP(Tg2576)) 中观察到的多动和认知缺陷。APP(Tg2576) 小鼠的运动活性明显高于野生型小鼠,但接受西替利嗪每日治疗的 APP(Tg2576) 小鼠的活性水平与野生型小鼠无差异。在游泳迷宫中,APP(Tg2576) 小鼠表现出明显更长的逃避潜伏期,但接受西替利嗪每日治疗的 APP(Tg2576) 小鼠的潜伏期与对照组无法区分。在最后一次训练试验后一小时进行的探测试验中,接受西替利嗪治疗的 APP(Tg2576) 小鼠在先前平台位置附近停留的时间更长,穿过该区域的次数也更多。APP(Tg2576) 小鼠在物体识别任务中也表现出明显的损伤,而急性西替利嗪(3.0mg/kg)治疗可逆转这种损伤。这些数据支持这样一种观点,即调节 H(3) 受体代表了治疗阿尔茨海默病的一种新颖且可行的治疗策略。