Putative neuroprotective agents in neuropsychiatric disorders

In many individuals with major neuropsychiatric disorders including depression, bipolar disorder and schizophrenia, their disease characteristics are consistent with a neuroprogressive illness. This includes progressive structural brain changes, cognitive and functional decline, poorer treatment res...

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Veröffentlicht in:Progress in neuro-psychopharmacology & biological psychiatry 2013-04, Vol.42, p.135-145
Hauptverfasser: Dodd, Seetal, Maes, Michael, Anderson, George, Dean, Olivia M., Moylan, Steven, Berk, Michael
Format: Artikel
Sprache:eng
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Zusammenfassung:In many individuals with major neuropsychiatric disorders including depression, bipolar disorder and schizophrenia, their disease characteristics are consistent with a neuroprogressive illness. This includes progressive structural brain changes, cognitive and functional decline, poorer treatment response and an increasing vulnerability to relapse with chronicity. The underlying molecular mechanisms of neuroprogression are thought to include neurotrophins and regulation of neurogenesis and apoptosis, neurotransmitters, inflammatory, oxidative and nitrosative stress, mitochondrial dysfunction, cortisol and the hypothalamic-pituitary-adrenal axis, and epigenetic influences. Knowledge of the involvement of each of these pathways implies that specific agents that act on some or multiple of these pathways may thus block this cascade and have neuroprotective properties. This paper reviews the potential of the most promising of these agents, including lithium and other known psychotropics, aspirin, minocycline, statins, N-acetylcysteine, leptin and melatonin. These agents are putative neuroprotective agents for schizophrenia and mood disorders. ► In many individuals major neuropsychiatric disorders are a neuroprogressive illness ► Structural brain changes, cognitive and functional decline and poor treatment response may occur ► Some treatments may have neuroprotective properties
ISSN:0278-5846
1878-4216
DOI:10.1016/j.pnpbp.2012.11.007