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Loss of circadian rhythm and light-induced suppression of pineal melatonin levels in Cry1 and Cry2 double-deficient mice.Cry1 和 Cry2 双缺失小鼠中昼夜节律的丧失和光诱导的松果体褪黑素水平的抑制。
Genes Cells. 2010 Oct;15(10):1063-71. doi: 10.1111/j.1365-2443.2010.01443.x. Epub 2010 Sep 5.
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Circadian rhythms and memory formation.昼夜节律与记忆形成。
Nat Rev Neurosci. 2010 Aug;11(8):577-88. doi: 10.1038/nrn2881.
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Post-training reversible inactivation of the hippocampus enhances novel object recognition memory.训练后可逆性海马体失活增强新物体识别记忆。
Learn Mem. 2010 Feb 26;17(3):155-60. doi: 10.1101/lm.1625310. Print 2010 Mar.
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Expression of the circadian clock gene Period2 in the hippocampus: possible implications for synaptic plasticity and learned behaviour.节律钟基因 Period2 在海马体中的表达:对突触可塑性和学习行为的潜在影响。
ASN Neuro. 2009 Jun 10;1(3):e00012. doi: 10.1042/AN20090020.
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Temporal dynamics of mouse hippocampal clock gene expression support memory processing.小鼠海马体时钟基因表达的时间动态支持记忆处理。
Hippocampus. 2010 Mar;20(3):377-88. doi: 10.1002/hipo.20637.
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Circadian oscillation of hippocampal MAPK activity and cAmp: implications for memory persistence.海马体丝裂原活化蛋白激酶活性和环磷酸腺苷的昼夜节律振荡:对记忆持久性的影响
Nat Neurosci. 2008 Sep;11(9):1074-82. doi: 10.1038/nn.2174.
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Morris water maze: procedures for assessing spatial and related forms of learning and memory.莫里斯水迷宫:评估空间及相关形式学习与记忆的程序。
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Context- but not familiarity-dependent forms of object recognition are impaired following excitotoxic hippocampal lesions in rats.在大鼠海马体受到兴奋性毒性损伤后,情境性——而非依赖熟悉度的物体识别形式——会受到损害。
Behav Neurosci. 2007 Feb;121(1):218-23. doi: 10.1037/0735-7044.121.1.218.
9
Ca2+ -stimulated adenylyl cyclases regulate ERK-dependent activation of MSK1 during fear conditioning.钙离子刺激的腺苷酸环化酶在恐惧条件反射过程中调节MSK1的ERK依赖性激活。
Neuron. 2007 Jan 4;53(1):79-89. doi: 10.1016/j.neuron.2006.11.024.
10
The HMG-CoA reductase inhibitor lovastatin reverses the learning and attention deficits in a mouse model of neurofibromatosis type 1.HMG-CoA还原酶抑制剂洛伐他汀可逆转1型神经纤维瘤病小鼠模型中的学习和注意力缺陷。
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海马区中丝裂原激活蛋白激酶和腺苷酸环化酶活性的日周期波动依赖于视交叉上核。

The diurnal oscillation of MAP (mitogen-activated protein) kinase and adenylyl cyclase activities in the hippocampus depends on the suprachiasmatic nucleus.

机构信息

Department of Pharmacology, School of Medicine, University of Washington, Seattle, Washington 98195-7750, USA.

出版信息

J Neurosci. 2011 Jul 20;31(29):10640-7. doi: 10.1523/JNEUROSCI.6535-10.2011.

DOI:10.1523/JNEUROSCI.6535-10.2011
PMID:21775607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3146036/
Abstract

Consolidation of hippocampus-dependent memory is dependent on activation of the cAMP/Erk/MAPK (mitogen-activated protein kinase) signal transduction pathway in the hippocampus. Recently, we discovered that adenylyl cyclase and MAPK activities undergo a circadian oscillation in the hippocampus and that inhibition of this oscillation impairs contextual memory. This suggests the interesting possibility that the persistence of hippocampus-dependent memory depends upon the reactivation of MAPK in the hippocampus during the circadian cycle. A key unanswered question is whether the circadian oscillation of this signaling pathway is intrinsic to the hippocampus or is driven by the master circadian clock in the suprachiasmatic nucleus (SCN). To address this question, we ablated the SCN of mice by electrolytic lesion and examined hippocampus-dependent memory as well as adenylyl cyclase and MAPK activities. Electrolytic lesion of the SCN 2 d after training for contextual fear memory reduced contextual memory measured 2 weeks after training, indicating that maintenance of contextual memory depends on the SCN. Spatial memory was also compromised in SCN-lesioned mice. Furthermore, the diurnal oscillation of adenylyl cyclase and MAPK activities in the hippocampus was destroyed by lesioning of the SCN. These data suggest that hippocampus-dependent long-term memory is dependent on the SCN-controlled oscillation of the adenylyl cyclase/MAPK pathway in the hippocampus.

摘要

海马体依赖型记忆的巩固依赖于海马体中 cAMP/Erk/MAPK(丝裂原激活蛋白激酶)信号转导途径的激活。最近,我们发现腺苷酸环化酶和 MAPK 活性在海马体中呈现昼夜节律性波动,而抑制这种波动会损害情景记忆。这表明一个有趣的可能性,即海马体依赖型记忆的持久性取决于在昼夜节律周期中 MAPK 在海马体中的再激活。一个关键的未解决的问题是,这种信号通路的昼夜节律性波动是海马体固有的,还是由视交叉上核(SCN)中的主生物钟驱动的。为了解决这个问题,我们通过电解损伤破坏了小鼠的 SCN,并检查了海马体依赖型记忆以及腺苷酸环化酶和 MAPK 活性。在进行情景恐惧记忆训练 2 天后,通过电解损伤 SCN 会降低训练 2 周后测量的情景记忆,表明维持情景记忆依赖于 SCN。SCN 损伤的小鼠的空间记忆也受到损害。此外,SCN 损伤破坏了海马体中腺苷酸环化酶和 MAPK 活性的昼夜节律性波动。这些数据表明,海马体依赖的长期记忆依赖于 SCN 控制的海马体中腺苷酸环化酶/MAPK 途径的振荡。