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本文引用的文献

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Selective activation of striatal fast-spiking interneurons during choice execution.选择执行期间纹状体快速放电中间神经元的选择性激活。
Neuron. 2010 Aug 12;67(3):466-79. doi: 10.1016/j.neuron.2010.06.034.
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Thalamic gating of corticostriatal signaling by cholinergic interneurons.胆碱能中间神经元对皮质纹状体信号的丘脑门控作用。
Neuron. 2010 Jul 29;67(2):294-307. doi: 10.1016/j.neuron.2010.06.017.
3
Distinct roles of synaptic transmission in direct and indirect striatal pathways to reward and aversive behavior.直接和间接纹状体通路在奖励和厌恶行为中的突触传递的不同作用。
Neuron. 2010 Jun 24;66(6):896-907. doi: 10.1016/j.neuron.2010.05.011.
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Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry.通过光遗传学控制基底神经节回路调节帕金森运动行为。
Nature. 2010 Jul 29;466(7306):622-6. doi: 10.1038/nature09159. Epub 2010 Jul 7.
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Competitive regulation of synaptic Ca2+ influx by D2 dopamine and A2A adenosine receptors.D2 多巴胺和 A2A 腺苷受体对突触 Ca2+内流的竞争性调节。
Nat Neurosci. 2010 Aug;13(8):958-66. doi: 10.1038/nn.2592. Epub 2010 Jul 4.
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Different corticostriatal integration in spiny projection neurons from direct and indirect pathways.不同投射神经元的皮质纹状体整合:直接通路和间接通路。
Front Syst Neurosci. 2010 Jun 10;4:15. doi: 10.3389/fnsys.2010.00015. eCollection 2010.
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Neural mechanisms for interacting with a world full of action choices.与充满行为选择的世界进行交互的神经机制。
Annu Rev Neurosci. 2010;33:269-98. doi: 10.1146/annurev.neuro.051508.135409.
8
Dynamics of synaptic transmission between fast-spiking interneurons and striatal projection neurons of the direct and indirect pathways.快速棘突中间神经元和纹状体投射神经元之间的直接和间接通路的突触传递动力学。
J Neurosci. 2010 Mar 3;30(9):3499-507. doi: 10.1523/JNEUROSCI.5139-09.2010.
9
MEF-2 regulates activity-dependent spine loss in striatopallidal medium spiny neurons.MEF-2 调节纹状体苍白球中间神经元中活性依赖的棘突丢失。
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The endocannabinoid 2-arachidonoylglycerol produced by diacylglycerol lipase alpha mediates retrograde suppression of synaptic transmission.二酰基甘油脂肪酶 α 产生的内源性大麻素 2-花生四烯酰甘油介导突触传递的逆行抑制。
Neuron. 2010 Feb 11;65(3):320-7. doi: 10.1016/j.neuron.2010.01.021.

多巴胺对纹状体投射系统的调制。

Modulation of striatal projection systems by dopamine.

机构信息

Laboratory of Systems Neuroscience, National Institute of Mental Health, Bethesda, Maryland 20892, USA.

出版信息

Annu Rev Neurosci. 2011;34:441-66. doi: 10.1146/annurev-neuro-061010-113641.

DOI:10.1146/annurev-neuro-061010-113641
PMID:21469956
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3487690/
Abstract

The basal ganglia are a chain of subcortical nuclei that facilitate action selection. Two striatal projection systems--so-called direct and indirect pathways--form the functional backbone of the basal ganglia circuit. Twenty years ago, investigators proposed that the striatum's ability to use dopamine (DA) rise and fall to control action selection was due to the segregation of D(1) and D(2) DA receptors in direct- and indirect-pathway spiny projection neurons. Although this hypothesis sparked a debate, the evidence that has accumulated since then clearly supports this model. Recent advances in the means of marking neural circuits with optical or molecular reporters have revealed a clear-cut dichotomy between these two cell types at the molecular, anatomical, and physiological levels. The contrast provided by these studies has provided new insights into how the striatum responds to fluctuations in DA signaling and how diseases that alter this signaling change striatal function.

摘要

基底神经节是一连串的皮质下核团,有助于动作选择。两个纹状体投射系统——所谓的直接和间接通路——构成了基底神经节回路的功能主干。二十年前,研究人员提出,纹状体利用多巴胺(DA)的上升和下降来控制动作选择的能力,是由于直接和间接通路棘突投射神经元中 D1 和 D2 DA 受体的分离。尽管这一假设引发了一场争论,但此后积累的证据清楚地支持了这一模型。利用光学或分子报告器标记神经回路的新方法的进展,在分子、解剖和生理水平上揭示了这两种细胞类型之间明显的二分法。这些研究提供的对比为纹状体如何响应 DA 信号波动以及改变这种信号的疾病如何改变纹状体功能提供了新的见解。