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干扰皮层网络:使用去氯氯氮平进行全神经元化学遗传操作的电生理后果

Perturbing cortical networks: electrophysiological consequences of pan-neuronal chemogenetic manipulations using deschloroclozapine.

作者信息

Kovács Péter, Beloate Lauren N, Zhang Nanyin

机构信息

Department of Biomedical Engineering, Pennsylvania State University, University Park, PA, United States.

Huck Institutes of the Life Sciences, Pennsylvania State University, University Park, PA, United States.

出版信息

Front Neurosci. 2024 Apr 25;18:1396978. doi: 10.3389/fnins.2024.1396978. eCollection 2024.

Abstract

INTRODUCTION

Chemogenetic techniques, specifically the use of Designer Receptors Exclusively Activated by Designer Drugs (DREADDs), have become invaluable tools in neuroscience research. Yet, the understanding of how Gq- and Gicoupled DREADDs alter local field potential (LFP) oscillations in vivo remains incomplete.

METHODS

This study investigates the in vivo electrophysiological effects of DREADD actuation by deschloroclozapine, on spontaneous firing rate and LFP oscillations recorded from the anterior cingulate cortex in lightly anesthetized male rats.

RESULTS

Unexpectedly, in response to the administration of deschloroclozapine, we observed inhibitory effects with pan-neuronal hM3D(Gq) stimulation, and excitatory effects with pan-neuronal hM4D(Gi) stimulation in a significant portion of neurons. These results emphasize the need to account for indirect perturbation effects at the local neuronal network level in vivo, particularly when not all neurons express the chemogenetic receptors uniformly. In the current study, for instance, the majority of cells that were transduced with both hM3D(Gq) and hM4D(Gi) were GABAergic. Moreover, we found that panneuronal cortical chemogenetic modulation can profoundly alter oscillatory neuronal activity, presenting a potential research tool or therapeutic strategy in several neuropsychiatric models and diseases.

DISCUSSION

These findings help to optimize the use of chemogenetic techniques in neuroscience research and open new possibilities for novel therapeutic strategies.

摘要

引言

化学遗传学技术,特别是仅由设计药物激活的设计受体(DREADDs)的使用,已成为神经科学研究中非常有价值的工具。然而,对于Gq和Gi偶联的DREADDs如何在体内改变局部场电位(LFP)振荡的理解仍不完整。

方法

本研究调查了在轻度麻醉的雄性大鼠中,去氯氯氮平激活DREADD对前扣带回皮质记录的自发放电率和LFP振荡的体内电生理效应。

结果

出乎意料的是,在给予去氯氯氮平后,我们观察到在大部分神经元中,泛神经元hM3D(Gq)刺激产生抑制作用,而泛神经元hM4D(Gi)刺激产生兴奋作用。这些结果强调了在体内局部神经元网络水平上考虑间接扰动效应的必要性,特别是当并非所有神经元都均匀表达化学遗传受体时。例如,在本研究中,同时转导hM3D(Gq)和hM4D(Gi)的大多数细胞是GABA能的。此外,我们发现泛神经元皮质化学遗传调制可深刻改变振荡性神经元活动,为几种神经精神疾病模型和疾病提供了潜在的研究工具或治疗策略。

讨论

这些发现有助于优化化学遗传学技术在神经科学研究中的应用,并为新的治疗策略开辟了新的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8768/11079238/f6d939baa028/fnins-18-1396978-g001.jpg

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