The use of chemogenetics in behavioural neuroscience: receptor variants, targeting approaches and caveats

被引:85
作者
Campbell, Erin J. [1 ]
Marchant, Nathan J. [1 ,2 ]
机构
[1] Univ Melbourne, Florey Dept Neurosci & Mental Hlth, Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia
[2] Vrije Univ Amsterdam, Med Ctr, Dept Anat & Neurosci, Amsterdam, Netherlands
基金
英国医学研究理事会;
关键词
PROTEIN-COUPLED RECEPTORS; CANINE ADENOVIRUS VECTORS; CLOZAPINE-N-OXIDE; CONCISE GUIDE; MAMMALIAN NEURONS; DESIGNER DRUGS; GENE-TRANSFER; IN-VIVO; AMYGDALA; CORTEX;
D O I
10.1111/bph.14146
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The last decade has seen major advances in neuroscience tools allowing us to selectively modulate cellular pathways in freely moving animals. Chemogenetic approaches such as designer receptors exclusively activated by designer drugs (DREADDs) permit the remote control of neuronal function by systemic drug administration. These approaches have dramatically advanced our understanding of the neural control of behaviour. Here, we review the different techniques and genetic approaches available for the restriction of chemogenetic receptors to defined neuronal populations. We highlight the use of a dual virus approach to target specific circuitries and the effectiveness of different routes of administration of designer drugs. Finally, we discuss the potential caveats associated with DREADDs including off-target effects of designer drugs, the effects of chronic chemogenetic receptor activation and the issue of collateral projections associated with DREADD activation and inhibition.
引用
收藏
页码:994 / 1003
页数:10
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