Gomez Juan L, Bonaventura Jordi, Lesniak Wojciech, Mathews William B, Sysa-Shah Polina, Rodriguez Lionel A, Ellis Randall J, Richie Christopher T, Harvey Brandon K, Dannals Robert F, Pomper Martin G, Bonci Antonello, Michaelides Michael
Biobehavioral Imaging and Molecular Neuropsychopharmacology Unit, National Institute on Drug Abuse (NIDA) Intramural Research Program, Baltimore, MD 21224, USA.
Department of Radiology, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
Science. 2017 Aug 4;357(6350):503-507. doi: 10.1126/science.aan2475.
The chemogenetic technology DREADD (designer receptors exclusively activated by designer drugs) is widely used for remote manipulation of neuronal activity in freely moving animals. DREADD technology posits the use of "designer receptors," which are exclusively activated by the "designer drug" clozapine N-oxide (CNO). Nevertheless, the in vivo mechanism of action of CNO at DREADDs has never been confirmed. CNO does not enter the brain after systemic drug injections and shows low affinity for DREADDs. Clozapine, to which CNO rapidly converts in vivo, shows high DREADD affinity and potency. Upon systemic CNO injections, converted clozapine readily enters the brain and occupies central nervous system-expressed DREADDs, whereas systemic subthreshold clozapine injections induce preferential DREADD-mediated behaviors.
化学遗传技术DREADD(仅由设计药物激活的设计受体)被广泛用于对自由活动动物的神经元活动进行远程操控。DREADD技术假定使用“设计受体”,这些受体仅由“设计药物”氯氮平N-氧化物(CNO)激活。然而,CNO在DREADD上的体内作用机制从未得到证实。全身注射药物后,CNO不会进入大脑,并且对DREADD的亲和力较低。CNO在体内迅速转化为氯氮平,氯氮平对DREADD具有高亲和力和效力。全身注射CNO后,转化后的氯氮平很容易进入大脑并占据中枢神经系统表达的DREADD,而全身注射亚阈值剂量的氯氮平会诱导优先的DREADD介导的行为。