Inflammatory factors contribute to depression and its comorbid conditions

Sci Signal. 2012 Oct 2;5(244):pe45. doi: 10.1126/scisignal.2003579.

Abstract

New perspectives have emerged regarding the processes associated with depressive disorders and their many comorbid conditions. Particular attention has been paid to the potential role of inflammatory factors in promoting these illnesses. These inflammatory responses include those elicited by pathogenic stimuli, as well as sterile inflammatory processes, such as those related to severe or chronic stress. These diverse challenges may activate common processes in which cytokines, which are inflammatory signaling molecules, provoke the dysregulation of several growth factors, including brain-derived neurotrophic factor, fibroblast growth factor-2, macrophage migration inhibitory factor, and erythropoietin. The result of such dysregulation favors the development of depressive disorders and their comorbid illnesses, such as heart disease, diabetes, autoimmune conditions, and poststroke depression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain-Derived Neurotrophic Factor / metabolism
  • Comorbidity
  • Cytokines / metabolism*
  • Depressive Disorder / epidemiology
  • Depressive Disorder / metabolism*
  • Depressive Disorder / psychology
  • Diabetes Mellitus / epidemiology
  • Diabetes Mellitus / metabolism*
  • Erythropoietin / metabolism
  • Fibroblast Growth Factor 2 / metabolism
  • Heart Diseases / epidemiology
  • Heart Diseases / metabolism*
  • Humans
  • Inflammation Mediators / metabolism*
  • Interleukin-6 / metabolism
  • Macrophage Migration-Inhibitory Factors / metabolism
  • Models, Biological
  • Models, Psychological
  • Signal Transduction
  • Stress, Psychological / metabolism
  • Stress, Psychological / psychology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Brain-Derived Neurotrophic Factor
  • Cytokines
  • Inflammation Mediators
  • Interleukin-6
  • Macrophage Migration-Inhibitory Factors
  • Tumor Necrosis Factor-alpha
  • Fibroblast Growth Factor 2
  • Erythropoietin