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第一组代谢型谷氨酸受体介导的马丁诺蒂细胞激活抑制人类皮层中的局部皮层回路。

Group I mGluR-Mediated Activation of Martinotti Cells Inhibits Local Cortical Circuitry in Human Cortex.

作者信息

Kroon Tim, Dawitz Julia, Kramvis Ioannis, Anink Jasper, Obermayer Joshua, Verhoog Matthijs B, Wilbers René, Goriounova Natalia A, Idema Sander, Baayen Johannes C, Aronica Eleonora, Mansvelder Huibert D, Meredith Rhiannon M

机构信息

Department of Integrative Neurophysiology, Center for Neurogenomics and Cognitive Research, VU University Amsterdam, Amsterdam, Netherlands.

Department of Neuropathology, Amsterdam Neuroscience, Amsterdam UMC, University of Amsterdam, Amsterdam, Netherlands.

出版信息

Front Cell Neurosci. 2019 Jul 11;13:315. doi: 10.3389/fncel.2019.00315. eCollection 2019.

Abstract

Group I metabotropic glutamate receptors (mGluRs) mediate a range of signaling and plasticity processes in the brain and are of growing importance as potential therapeutic targets in clinical trials for neuropsychiatric and neurodevelopmental disorders (NDDs). Fundamental knowledge regarding the functional effects of mGluRs upon pyramidal neurons and interneurons is derived largely from rodent brain, and their effects upon human neurons are predominantly untested. We therefore addressed how group I mGluRs affect microcircuits in human neocortex. We show that activation of group I mGluRs elicits action potential firing in Martinotti cells, which leads to increased synaptic inhibition onto neighboring neurons. Some other interneurons, including fast-spiking interneurons, are depolarized but do not fire action potentials in response to group I mGluR activation. Furthermore, we confirm the existence of group I mGluR-mediated depression of excitatory synapses in human pyramidal neurons. We propose that the strong increase in inhibition and depression of excitatory synapses onto layer 2/3 pyramidal neurons upon group I mGluR activation likely results in a shift in the balance between excitation and inhibition in the human cortical network.

摘要

I 型代谢型谷氨酸受体(mGluRs)介导大脑中的一系列信号传导和可塑性过程,并且作为神经精神疾病和神经发育障碍(NDDs)临床试验中的潜在治疗靶点,其重要性日益增加。关于 mGluRs 对锥体神经元和中间神经元功能影响的基础知识主要来自啮齿动物大脑,而它们对人类神经元的影响大多未经测试。因此,我们研究了 I 型 mGluRs 如何影响人类新皮层中的微电路。我们发现,I 型 mGluRs 的激活引发马丁诺蒂细胞的动作电位发放,这导致对相邻神经元的突触抑制增加。其他一些中间神经元,包括快发放中间神经元,会发生去极化,但对 I 型 mGluR 激活不产生动作电位。此外,我们证实了人类锥体神经元中存在 I 型 mGluR 介导的兴奋性突触抑制。我们提出,I 型 mGluR 激活后,对第 2/3 层锥体神经元的兴奋性突触抑制和抑制作用的强烈增加可能导致人类皮质网络中兴奋与抑制平衡的转变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3698/6637283/2e4cd208d4d2/fncel-13-00315-g001.jpg

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