Chemogenetics revealed: DREADD occupancy and activation via converted clozapine

Juan L. Gomez(National Institute on Drug Abuse), Jordi Bonaventura(National Institute on Drug Abuse), Wojciech G. Lesniak(Johns Hopkins University), William B. Mathews(Johns Hopkins University), Polina Sysa‐Shah(Johns Hopkins University), Lionel A. Rodriguez(National Institute on Drug Abuse), Randall J. Ellis(National Institute on Drug Abuse), Christopher T. Richie(Immungenetics (Germany)), Brandon K. Harvey(Immungenetics (Germany)), Robert F. Dannals(Johns Hopkins University), Martin G. Pomper(Johns Hopkins University), Antonello Bonci(Synaptic Research (United States)), Michael Michaelides(National Institute on Drug Abuse)
Science
August 3, 2017
Cited by 1,025Open Access
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Abstract

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.


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