Olanzapine: A potent agonist at the hM4D(Gi) DREADD amenable to clinical translation of chemogenetics.


Journal

Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440

Informations de publication

Date de publication:
04 2019
Historique:
received: 22 11 2018
accepted: 05 03 2019
entrez: 20 4 2019
pubmed: 20 4 2019
medline: 6 5 2020
Statut: epublish

Résumé

Designer receptors exclusively activated by designer drugs (DREADDs) derived from muscarinic receptors not only are a powerful tool to test causality in basic neuroscience but also are potentially amenable to clinical translation. A major obstacle, however, is that the widely used agonist clozapine

Identifiants

pubmed: 31001591
doi: 10.1126/sciadv.aaw1567
pii: aaw1567
pmc: PMC6469940
doi:

Substances chimiques

Designer Drugs 0
Receptor, Muscarinic M4 0
Serotonin Uptake Inhibitors 0
Olanzapine N7U69T4SZR

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

eaaw1567

Subventions

Organisme : Medical Research Council
ID : G0802158
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0900613
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0501424
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L01095X/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0400136
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0600368
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0400627
Pays : United Kingdom
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : G116/147
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0601440
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 209807/Z/17/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 212285/Z/18/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : G9805989
Pays : United Kingdom

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Auteurs

Mikail Weston (M)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London, UK.

Teresa Kaserer (T)

Cancer Research UK Cancer Therapeutics Unit, The Institute of Cancer Research, London SM2 5NG, UK.

Angela Wu (A)

Department of Pharmacology & Clinical Pharmacology, The University of Auckland, Auckland, New Zealand.

Alexandre Mouravlev (A)

Department of Pharmacology & Clinical Pharmacology, The University of Auckland, Auckland, New Zealand.

Jenna C Carpenter (JC)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London, UK.

Albert Snowball (A)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London, UK.

Samuel Knauss (S)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London, UK.

Melanie von Schimmelmann (M)

Ovid Therapeutics, Inc., 1460 Broadway, New York, NY 10036, USA.

Matthew J During (MJ)

Ovid Therapeutics, Inc., 1460 Broadway, New York, NY 10036, USA.

Gabriele Lignani (G)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London, UK.

Stephanie Schorge (S)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London, UK.

Deborah Young (D)

Department of Pharmacology & Clinical Pharmacology, The University of Auckland, Auckland, New Zealand.

Dimitri M Kullmann (DM)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London, UK.

Andreas Lieb (A)

Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London, UK.

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Classifications MeSH