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通过仅由设计药物特异性激活的化学遗传设计受体来解析行为输出。

Resolving Behavioral Output via Chemogenetic Designer Receptors Exclusively Activated by Designer Drugs.

作者信息

Burnett C Joseph, Krashes Michael J

机构信息

Diabetes, Endocrinology and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland 21224, and Brown University-National Institutes of Health Graduate Partnerships Program, Providence, Rhode Island 02912.

Diabetes, Endocrinology and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland 21224, and

出版信息

J Neurosci. 2016 Sep 7;36(36):9268-82. doi: 10.1523/JNEUROSCI.1333-16.2016.

Abstract

Designer receptors exclusively activated by designer drugs (DREADDs) have proven to be highly effective neuromodulatory tools for the investigation of neural circuits underlying behavioral outputs. They exhibit a number of advantages: they rely on cell-specific manipulations through canonical intracellular signaling pathways, they are easy and cost-effective to implement in a laboratory setting, and they are easily scalable for single-region or full-brain manipulations. On the other hand, DREADDs rely on ligand-G-protein-coupled receptor interactions, leading to coarse temporal dynamics. In this review we will provide a brief overview of DREADDs, their implementation, and the advantages and disadvantages of their use in animal systems. We also will provide numerous examples of their use across a broad variety of biomedical research fields.

摘要

仅由设计药物激活的设计受体(DREADDs)已被证明是研究行为输出背后神经回路的高效神经调节工具。它们具有许多优点:通过经典细胞内信号通路依赖于细胞特异性操作,在实验室环境中易于实施且成本效益高,并且易于扩展用于单区域或全脑操作。另一方面,DREADDs依赖于配体 - G蛋白偶联受体相互作用,导致时间动态较为粗糙。在本综述中,我们将简要概述DREADDs、它们的实施方法以及在动物系统中使用它们的优缺点。我们还将提供它们在广泛的生物医学研究领域中使用的大量示例。

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