• 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
Discovering Memory: Using Sea Slugs to Teach Learning and Memory.探索记忆:利用海蛞蝓讲授学习与记忆
J Undergrad Neurosci Educ. 2020 Dec 31;19(1):R19-R22. eCollection 2020 Fall.
2
Mediation of classical conditioning in Aplysia californica by long-term potentiation of sensorimotor synapses.通过感觉运动突触的长时程增强介导加州海兔的经典条件反射。
Science. 1997 Oct 17;278(5337):467-71. doi: 10.1126/science.278.5337.467.
3
Facilitation of hippocampal long-term potentiation and reactivation of latent HIV-1 via AMPK activation: Common mechanism of action linking learning, memory, and the potential eradication of HIV-1.通过 AMPK 激活促进海马长时程增强和潜伏 HIV-1 的再激活:连接学习、记忆和潜在 HIV-1 根除的共同作用机制。
Med Hypotheses. 2018 Jul;116:61-73. doi: 10.1016/j.mehy.2018.04.018. Epub 2018 Apr 22.
4
Inverse synaptic tagging: An inactive synapse-specific mechanism to capture activity-induced Arc/arg3.1 and to locally regulate spatial distribution of synaptic weights.反向突触标签:一种非活动突触特异性机制,用于捕获活性诱导的 Arc/arg3.1,并在局部调节突触权重的空间分布。
Semin Cell Dev Biol. 2018 May;77:43-50. doi: 10.1016/j.semcdb.2017.09.025. Epub 2017 Sep 23.
5
Regulation of late-phase LTP and long-term memory in normal and aging hippocampus: role of secreted proteins tPA and BDNF.正常及衰老海马体中晚期长时程增强和长期记忆的调节:分泌蛋白组织型纤溶酶原激活剂和脑源性神经营养因子的作用
Ageing Res Rev. 2004 Nov;3(4):407-30. doi: 10.1016/j.arr.2004.07.002.
6
Protein synthesis is required for the enhancement of long-term potentiation and long-term memory by spaced training.间隔训练增强长时程增强效应和长期记忆需要蛋白质合成。
J Neurophysiol. 2002 Jun;87(6):2770-7. doi: 10.1152/jn.2002.87.6.2770.
7
Synaptic remodeling, synaptic growth and the storage of long-term memory in Aplysia.海兔的突触重塑、突触生长与长期记忆存储
Prog Brain Res. 2008;169:179-98. doi: 10.1016/S0079-6123(07)00010-6.
8
Low-frequency-induced synaptic potentiation: a paradigm shift in the field of memory-related plasticity mechanisms?低频诱导的突触增强:记忆相关可塑性机制领域的范式转变?
Hippocampus. 2010 Jan;20(1):29-35. doi: 10.1002/hipo.20611.
9
Synapse-specific, long-term facilitation of aplysia sensory to motor synapses: a function for local protein synthesis in memory storage.海兔感觉运动突触特异性的长期易化:局部蛋白质合成在记忆存储中的作用。
Cell. 1997 Dec 26;91(7):927-38. doi: 10.1016/s0092-8674(00)80484-5.
10
Hippocampal long-term potentiation that is elicited by perforant path stimulation or that occurs in conjunction with spatial learning is tightly controlled by beta-adrenoreceptors and the locus coeruleus.由穿通通路刺激引发或与空间学习同时发生的海马体长期增强效应,受到β-肾上腺素能受体和蓝斑核的严格控制。
Hippocampus. 2015 Nov;25(11):1285-98. doi: 10.1002/hipo.22436. Epub 2015 Apr 2.

引用本文的文献

1
Virtual was the Reality in Neuroscience Education during the COVID-19 Pandemic.在新冠疫情期间,虚拟教学成为神经科学教育中的现实。
J Undergrad Neurosci Educ. 2020 Dec 31;19(1):E1-E2. eCollection 2020 Fall.

本文引用的文献

1
Molecular Mechanisms of the Memory Trace.记忆痕迹的分子机制。
Trends Neurosci. 2019 Jan;42(1):14-22. doi: 10.1016/j.tins.2018.10.005. Epub 2018 Oct 31.
2
Plasticity of intrinsic neuronal excitability.内在神经元兴奋性的可塑性。
Curr Opin Neurobiol. 2019 Feb;54:73-82. doi: 10.1016/j.conb.2018.09.001. Epub 2018 Sep 19.
3
The molecular biology of memory: cAMP, PKA, CRE, CREB-1, CREB-2, and CPEB.记忆的分子生物学:cAMP、PKA、CRE、CREB-1、CREB-2 和 CPEB。
Mol Brain. 2012 May 14;5:14. doi: 10.1186/1756-6606-5-14.
4
Making memories last: the synaptic tagging and capture hypothesis.让记忆持久:突触标记和捕获假说。
Nat Rev Neurosci. 2011 Jan;12(1):17-30. doi: 10.1038/nrn2963.
5
Synapse-specific, long-term facilitation of aplysia sensory to motor synapses: a function for local protein synthesis in memory storage.海兔感觉运动突触特异性的长期易化:局部蛋白质合成在记忆存储中的作用。
Cell. 1997 Dec 26;91(7):927-38. doi: 10.1016/s0092-8674(00)80484-5.
6
Synaptic tagging and long-term potentiation.突触标记与长时程增强
Nature. 1997 Feb 6;385(6616):533-6. doi: 10.1038/385533a0.
7
Calcium-mediated reduction of ionic currents: a biophysical memory trace.钙介导的离子电流减少:一种生物物理记忆痕迹。
Science. 1984 Nov 30;226(4678):1037-45. doi: 10.1126/science.6093258.
8
Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path.在麻醉兔的齿状区,刺激穿通通路后突触传递的长时程增强。
J Physiol. 1973 Jul;232(2):331-56. doi: 10.1113/jphysiol.1973.sp010273.

探索记忆:利用海蛞蝓讲授学习与记忆

Discovering Memory: Using Sea Slugs to Teach Learning and Memory.

作者信息

Riegel Devon C

机构信息

School of Psychology and Neuroscience, University of St. Andrews, St. Andrews, UK KY16 9JP.

出版信息

J Undergrad Neurosci Educ. 2020 Dec 31;19(1):R19-R22. eCollection 2020 Fall.

PMID:33880108
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8040845/
Abstract

Research on the sea slug has played a key role in unraveling the molecular mechanisms for learning and memory. In this system, synapses exhibiting long-term potentiation provide an ideal experimental platform for uncovering conserved principles. This review will discuss a 1997 study published in the journal which explored the means by which synapse-specific long-term potentiation occurs and its reliance on local protein synthesis. This study, conducted by Kelsey Martin and colleagues working in the Kandel laboratory, also explored synaptic capture: the mechanism by which a stimulated synapse recruits proteins from another, such that both undergo long-term potentiation. The authors discovered that synaptic capture does not require local protein synthesis, which led to further research on this mechanism. This study introduces undergraduates to a variety of research methods. Additionally, educators may use this paper as an introduction to the body of work produced by the Kandel laboratory and the field of learning and memory more generally. Advanced analyses of this research by upper level undergraduates may provide insights into competing theories for cellular mechanisms of long-term memory, presenting the opportunity to discuss disagreements within the scientific community.

摘要

对海蛞蝓的研究在揭示学习和记忆的分子机制方面发挥了关键作用。在这个系统中,表现出长期增强效应的突触为揭示保守原理提供了一个理想的实验平台。这篇综述将讨论1997年发表在该期刊上的一项研究,该研究探讨了突触特异性长期增强效应发生的方式及其对局部蛋白质合成的依赖。这项由凯尔西·马丁及其在坎德尔实验室工作的同事进行的研究,还探讨了突触捕获:即受刺激的突触从另一个突触招募蛋白质的机制,从而使两者都经历长期增强效应。作者发现突触捕获不需要局部蛋白质合成,这引发了对该机制的进一步研究。这项研究向本科生介绍了多种研究方法。此外,教育工作者可以将本文作为对坎德尔实验室以及更广泛的学习和记忆领域所产生的研究成果的介绍。高年级本科生对这项研究的深入分析可能会为长期记忆的细胞机制的竞争理论提供见解,从而提供讨论科学界内分歧的机会。