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作者单位:Erica M. Richards (1) Daniel C. Mathews (1) (3) David A. Luckenbaugh (1) Dawn F. Ionescu (1) (4) Rodrigo Machado-Vieira (1) Mark J. Niciu (1) Wallace C. Duncan (1) Neal M. Nolan (1) Jose A. Franco-Chaves (1) (5) Thomas Hudzik (2) (6) Carla Maciag (2) (7) Shuang Li (2) Alan Cross (2) Mark A. Smith (2) Carlos A. Zarate Jr. (1)
1. Experimental Therapeutics and Pathophysiology Branch, Department of Health and Human Services, National Institute of Mental Health, National Institutes of Health, 10 Center Drive CRC, Room 7-5545, Bethesda, MD, 20892, USA 3. Lundbeck LLC, Chicago, IL, USA 4. Massachusetts General Hospital, Boston, MA, USA 5. Veteran Affairs Caribbean Healthcare System, San Juan, Puerto Rico 2. AstraZeneca Neuroscience Innovative Medicines, Cambridge, MA, USA 6. AbbVie, Chicago, IL, USA 7. Sage Therapeutics, Cambridge, MA, USA
刊物类别:Biomedical and Life Sciences
刊物主题:Biomedicine Pharmacology and Toxicology Psychiatry
出版者:Springer Berlin / Heidelberg
ISSN:1432-2072
文摘
Rationale Patients with anxious major depressive disorder (AMDD) have more severe symptoms and poorer treatment response than patients with non-AMDD. Increasing evidence implicates the endogenous opioid system in the pathophysiology of depression. AZD2327 is a selective delta opioid receptor (DOR) agonist with anxiolytic and antidepressant activity in animal models.