| Literature DB >> 25003554 |
Abstract
Inflammatory cytokines can sometimes trigger depression in humans, are often associated with depression, and can elicit some behaviors in animals that are homologous to major depression. Moreover, these cytokines can affect monoaminergic and glutamatergic systems, supporting an overlapping pathoetiology with major depression. This suggests that there could be a specific major depression subtype, inflammatory cytokine-associated depression (ICAD), which may require different therapeutic approaches. However, most people do not develop depression, even when exposed to sustained elevations in inflammatory cytokines. Thus several vulnerabilities and sources of resilience to inflammation-associated depression have been identified. These range from genetic differences in neurotrophic and serotonergic systems to sleep quality and omega-3 fatty acid levels. Replicating these sources of resilience as treatments could be one approach for preventing "ICAD". This article is part of a Special Issue entitled SI: Neuroimmunology in Health And Disease.Entities:
Keywords: Cytokine; Depression; Interferon; Interleukin; Mood; Vulnerability
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Year: 2014 PMID: 25003554 PMCID: PMC4284141 DOI: 10.1016/j.brainres.2014.06.032
Source DB: PubMed Journal: Brain Res ISSN: 0006-8993 Impact factor: 3.252