Minocycline As a Candidate Treatment
Behavioural Brain Research 235 (2012) 302–317 Contents lists available at SciVerse ScienceDirect Behavioural Brain Research j ournal homepage: www.elsevier.com/locate/bbr Review Novel therapeutic targets in depression: Minocycline as a candidate treatment a,b c,d c,d f,g Joanna K. Soczynska , Rodrigo B. Mansur , Elisa Brietzke , Walter Swardfager , a,b,e b b Sidney H. Kennedy , Hanna O. Woldeyohannes , Alissa M. Powell , b a,b,e,f,∗ Marena S. Manierka , Roger S. McIntyre a Institute of Medical Science, University of Toronto, Toronto, Canada b Mood Disorders Psychopharmacology Unit, University Health Network, Toronto, Canada c Program of Recognition and Intervention in Individuals in at Risk Mental States (PRISMA), Department of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil d Interdisciplinary Laboratory of Clinical Neurosciences (LINC), Department of Psychiatry, Universidade Federal de São Paulo, São Paulo, Brazil e Department of Psychiatry, University of Toronto, Toronto, Canada f Departments of Pharmacology and Toxicology, University of Toronto, Toronto, Canada g Neuropsychopharmacology Research Group, Sunnybrook Health Sciences Centre, Toronto, Canada h i g h l i g h t s Regional cell loss and brain atrophy in mood disorders may be a consequence of impaired neuroplasticity. Neuroplasticity is regulated by neurotrophic, inflammatory, oxidative, glutamatergic pathways. Abnormalities in these systems are implicated in the pathophysiology of mood disorders. Minocycline exerts effects on neuroplasticity and targets these interacting systems. Evidence indicates that minocycline may be a viable treatment option for mood disorders. a r t i c l e i n f o a b s t r a c t Article history: Mood disorders are marked by high rates of non-recovery, recurrence, and chronicity, which are insuf- Received 1 December 2011 ficiently addressed by current therapies.
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