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本文引用的文献

1
Dual involvement of G-substrate in motor learning revealed by gene deletion.基因缺失揭示G底物在运动学习中的双重作用。
Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3525-30. doi: 10.1073/pnas.0813341106. Epub 2009 Feb 13.
2
State-dependence of climbing fiber-driven calcium transients in Purkinje cells.浦肯野细胞中攀缘纤维驱动的钙瞬变的状态依赖性。
Neuroscience. 2009 Sep 1;162(3):694-701. doi: 10.1016/j.neuroscience.2008.12.044. Epub 2009 Jan 3.
3
Lipid mediators in health and disease: enzymes and receptors as therapeutic targets for the regulation of immunity and inflammation.健康与疾病中的脂质介质:作为调节免疫和炎症治疗靶点的酶与受体
Annu Rev Pharmacol Toxicol. 2009;49:123-50. doi: 10.1146/annurev.pharmtox.011008.145616.
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A positive feedback signal transduction loop determines timing of cerebellar long-term depression.一个正反馈信号转导环路决定小脑长时程抑制的时机。
Neuron. 2008 Aug 28;59(4):608-20. doi: 10.1016/j.neuron.2008.06.026.
5
Cytosolic PLA2(alpha) activation in Purkinje neurons and its role in AMPA-receptor trafficking.浦肯野神经元中胞质型磷脂酶A2(α)的激活及其在AMPA受体转运中的作用。
J Cell Sci. 2008 Sep 15;121(Pt 18):3015-24. doi: 10.1242/jcs.032987. Epub 2008 Aug 19.
6
Enhancement of both long-term depression induction and optokinetic response adaptation in mice lacking delphilin.在缺乏德尔菲林的小鼠中,长时程抑制诱导和视动反应适应性均增强。
PLoS One. 2008 May 28;3(5):e2297. doi: 10.1371/journal.pone.0002297.
7
Ca2+ requirements for cerebellar long-term synaptic depression: role for a postsynaptic leaky integrator.小脑长期突触抑制对钙离子的需求:突触后漏电积分器的作用
Neuron. 2007 Jun 7;54(5):787-800. doi: 10.1016/j.neuron.2007.05.014.
8
Biophysical model of AMPA receptor trafficking and its regulation during long-term potentiation/long-term depression.AMPA受体转运的生物物理模型及其在长时程增强/长时程抑制过程中的调控
J Neurosci. 2006 Nov 22;26(47):12362-73. doi: 10.1523/JNEUROSCI.3601-06.2006.
9
Bidirectional trafficking of prostaglandin E2 receptors involved in long-term potentiation in visual cortex.参与视觉皮层长时程增强的前列腺素E2受体的双向运输
J Neurosci. 2006 Oct 4;26(40):10209-21. doi: 10.1523/JNEUROSCI.3028-06.2006.
10
ERK1/2 but not p38 MAP kinase is essential for the long-term depression in mouse cerebellar slices.细胞外信号调节激酶1/2而非p38丝裂原活化蛋白激酶对小鼠小脑切片中的长时程抑制至关重要。
Eur J Neurosci. 2006 Sep;24(6):1617-22. doi: 10.1111/j.1460-9568.2006.05055.x.

细胞质型磷脂酶 A2α-环氧化酶-2 级联中的脂质信号转导调节小脑长时程抑制和运动学习。

Lipid signaling in cytosolic phospholipase A2alpha-cyclooxygenase-2 cascade mediates cerebellar long-term depression and motor learning.

机构信息

Ito Laboratory and Nagao Laboratory, RIKEN Brain Science Institute, Saitama 351-0198, Japan.

出版信息

Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):3198-203. doi: 10.1073/pnas.0915020107. Epub 2010 Jan 28.

DOI:10.1073/pnas.0915020107
PMID:20133605
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2840314/
Abstract

In this study, we show the crucial roles of lipid signaling in long-term depression (LTD), that is, synaptic plasticity prevailing in cerebellar Purkinje cells. In mouse brain slices, we found that cPLA(2)alpha knockout blocked LTD induction, which was rescued by replenishing arachidonic acid (AA) or prostaglandin (PG) D(2) or E(2). Moreover, cyclooxygenase (COX)-2 inhibitors block LTD, which is rescued by supplementing PGD(2)/E(2). The blockade or rescue occurs when these reagents are applied within a time window of 5-15 min following the onset of LTD-inducing stimulation. Furthermore, PGD(2)/E(2) facilitates the chemical induction of LTD by a PKC activator but is unable to rescue the LTD blocked by a PKC inhibitor. We conclude that PGD(2)/E(2) mediates LTD jointly with PKC, and suggest possible pathways for their interaction. Finally, we demonstrate in awake mice that cPLA(2)alpha deficiency or COX-2 inhibition attenuates short-term adaptation of optokinetic eye movements, supporting the view that LTD underlies motor learning.

摘要

在这项研究中,我们展示了脂质信号在长时程抑制(LTD)中的关键作用,即小脑浦肯野细胞中占主导地位的突触可塑性。在小鼠脑切片中,我们发现 cPLA2α 敲除阻止了 LTD 的诱导,而补充花生四烯酸(AA)或前列腺素(PG)D2 或 E2 则可以挽救。此外,环氧化酶(COX)-2 抑制剂阻断 LTD,而补充 PGD2/E2 则可以挽救。这些试剂在 LTD 诱导刺激开始后的 5-15 分钟时间窗口内应用时会发生阻断或挽救。此外,PGD2/E2 通过 PKC 激活剂促进 LTD 的化学诱导,但不能挽救 PKC 抑制剂阻断的 LTD。我们得出结论,PGD2/E2 与 PKC 共同介导 LTD,并提出了它们相互作用的可能途径。最后,我们在清醒的小鼠中证明,cPLA2α 缺失或 COX-2 抑制减弱了光运动眼球运动的短期适应,支持 LTD 是运动学习的基础这一观点。