Campbell Erin J, Marchant Nathan J
The Florey Institute of Neuroscience and Mental Health, Florey Department of Neuroscience and Mental Health, The University of Melbourne, Parkville, VIC, Australia.
Department of Anatomy & Neurosciences, VU University Medical Center, Amsterdam, The Netherlands.
Br J Pharmacol. 2018 Apr;175(7):994-1003. doi: 10.1111/bph.14146. Epub 2018 Feb 26.
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.
在过去十年中,神经科学工具取得了重大进展,使我们能够在自由活动的动物中选择性地调节细胞通路。诸如仅由设计药物激活的设计受体(DREADDs)等化学遗传学方法,可通过全身给药实现对神经元功能的远程控制。这些方法极大地推进了我们对行为神经控制的理解。在这里,我们回顾了可用于将化学遗传学受体限制在特定神经元群体的不同技术和遗传方法。我们强调了使用双病毒方法靶向特定神经回路以及设计药物不同给药途径的有效性。最后,我们讨论了与DREADDs相关的潜在问题,包括设计药物的脱靶效应、慢性化学遗传学受体激活的影响以及与DREADD激活和抑制相关的侧支投射问题。