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Glutamatergic signaling by mesolimbic dopamine neurons in the nucleus accumbens.中脑边缘多巴胺神经元在伏隔核中的谷氨酸能信号传递。
J Neurosci. 2010 May 19;30(20):7105-10. doi: 10.1523/JNEUROSCI.0265-10.2010.
2
Activity-dependent regulation of synapses by retrograde messengers.逆行信使对突触的活动依赖性调节。
Neuron. 2009 Jul 30;63(2):154-70. doi: 10.1016/j.neuron.2009.06.021.
3
Metaplasticity of hypothalamic synapses following in vivo challenge.体内刺激后下丘脑突触的元可塑性
Neuron. 2009 Jun 25;62(6):839-49. doi: 10.1016/j.neuron.2009.05.027.
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Retrograde opioid signaling regulates glutamatergic transmission in the hypothalamus.逆向阿片类信号传导调节下丘脑的谷氨酸能传递。
J Neurosci. 2009 Jun 3;29(22):7349-58. doi: 10.1523/JNEUROSCI.0381-09.2009.
5
Noradrenergic control of associative synaptic plasticity by selective modulation of instructive signals.通过对指导性信号的选择性调节实现去甲肾上腺素能对联合突触可塑性的控制。
Neuron. 2009 Apr 16;62(1):112-22. doi: 10.1016/j.neuron.2009.02.022.
6
Glucocorticoids regulate glutamate and GABA synapse-specific retrograde transmission via divergent nongenomic signaling pathways.糖皮质激素通过不同的非基因组信号通路调节谷氨酸和γ-氨基丁酸突触特异性逆行传递。
J Neurosci. 2009 Jan 14;29(2):393-401. doi: 10.1523/JNEUROSCI.4546-08.2009.
7
Glycinergic transmission shaped by the corelease of GABA in a mammalian auditory synapse.在哺乳动物听觉突触中,由γ-氨基丁酸(GABA)共释放所塑造的甘氨酸能传递。
Neuron. 2008 Feb 28;57(4):524-35. doi: 10.1016/j.neuron.2007.12.010.
8
Functional blockage of the cannabinoid receptor type 1 evokes a kappa-opiate-dependent analgesia.功能性阻断大麻素受体 1 可引起κ阿片依赖的镇痛。
J Neurochem. 2007 Dec;103(6):2629-39. doi: 10.1111/j.1471-4159.2007.05000.x.
9
Integration of asynchronously released quanta prolongs the postsynaptic spike window.异步释放量子的整合延长了突触后尖峰窗口。
J Neurosci. 2007 Jun 20;27(25):6684-91. doi: 10.1523/JNEUROSCI.0934-07.2007.
10
Dendritic release of retrograde messengers controls synaptic transmission in local neocortical networks.树突释放逆行信使控制局部新皮层网络中的突触传递。
Neuroscientist. 2005 Aug;11(4):334-44. doi: 10.1177/1073858405275827.

内源性大麻素对顺行和逆行传递的双重调节。

Dual regulation of anterograde and retrograde transmission by endocannabinoids.

机构信息

Hotchkiss Brain Institute and the Department of Physiology and Pharmacology, University of Calgary, Calgary, Alberta T2N 4N1, Canada.

出版信息

J Neurosci. 2011 Aug 17;31(33):12011-20. doi: 10.1523/JNEUROSCI.2925-11.2011.

DOI:10.1523/JNEUROSCI.2925-11.2011
PMID:21849561
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6623194/
Abstract

Endocannabinoids (eCBs) are feedback messengers in the nervous system that act at the presynaptic nerve terminal to inhibit transmitter release. Here we report that in brain slices from rat, eCBs are released from vasopressin (VP) neurons in the paraventricular nucleus of the hypothalamus following coincident bursts of presynaptic and postsynaptic spiking. eCBs transiently depress glutamate release from excitatory terminals and, in doing so, prevent the synapses from undergoing long-term depression (LTD). Specifically, we show that blockade of CB1 receptors unmasks LTD following coincident presynaptic and postsynaptic activity. This LTD is presynaptic in nature, but requires the release of the opioid peptide dynorphin from the postsynaptic neuron. Dynorphin release and subsequent LTD require the activation of postsynaptic metabotropic glutamate receptors (mGluRs). Our findings indicate that eCBs, by transiently depressing glutamate release, limit mGluR activation and indirectly gate release of dynorphin from the postsynaptic neuron. We propose that eCBs, in addition to their well described role in the rapid modulation of transmitter release from the nerve terminal, also regulate the release of other retrograde transmitters and thus encode for multiple temporal windows of synaptic plasticity.

摘要

内源性大麻素 (eCBs) 是神经系统中的反馈信使,作用于突触前神经末梢以抑制递质释放。在这里,我们报告在大鼠脑片中,在下丘脑室旁核的加压素 (VP) 神经元中,在突触前和突触后放电的同时爆发会释放 eCBs。eCBs 会短暂抑制谷氨酸从兴奋性末梢释放,并由此防止突触发生长时程抑制 (LTD)。具体而言,我们发现阻断 CB1 受体可在突触前和突触后活动同时发生时揭示 LTD。这种 LTD 本质上是突触前的,但需要从突触后神经元释放阿片肽 dynorphin。dynorphin 释放和随后的 LTD 需要激活突触后代谢型谷氨酸受体 (mGluRs)。我们的研究结果表明,eCBs 通过短暂抑制谷氨酸释放,限制 mGluR 的激活,并间接控制 dynorphin 从突触后神经元的释放。我们提出,eCBs 除了在快速调节神经末梢递质释放方面的作用外,还调节其他逆行递质的释放,从而编码多个突触可塑性的时间窗口。