Mood and memory deficits in a model of Gulf War illness are linked with reduced neurogenesis, partial neuron loss, and mild inflammation in the hippocampus

Neuropsychopharmacology. 2013 Nov;38(12):2348-62. doi: 10.1038/npp.2013.158. Epub 2013 Jun 28.

Abstract

Impairments in mood and cognitive function are the key brain abnormalities observed in Gulf war illness (GWI), a chronic multisymptom health problem afflicting ∼25% of veterans who served in the Persian Gulf War-1. Although the precise cause of GWI is still unknown, combined exposure to a nerve gas prophylaxis drug pyridostigmine bromide (PB) and pesticides DEET and permethrin during the war has been proposed as one of the foremost causes of GWI. We investigated the effect of 4 weeks of exposure to Gulf war illness-related (GWIR) chemicals in the absence or presence of mild stress on mood and cognitive function, dentate gyrus neurogenesis, and neurons, microglia, and astrocytes in the hippocampus. Combined exposure to low doses of GWIR chemicals PB, DEET, and permethrin induced depressive- and anxiety-like behavior and spatial learning and memory dysfunction. Application of mild stress in the period of exposure to chemicals exacerbated the extent of mood and cognitive dysfunction. Furthermore, these behavioral impairments were associated with reduced hippocampal volume and multiple cellular alterations such as chronic reductions in neural stem cell activity and neurogenesis, partial loss of principal neurons, and mild inflammation comprising sporadic occurrence of activated microglia and significant hypertrophy of astrocytes. The results show the first evidence of an association between mood and cognitive dysfunction and hippocampal pathology epitomized by decreased neurogenesis, partial loss of principal neurons, and mild inflammation in a model of GWI. Hence, treatment strategies that are efficacious for enhancing neurogenesis and suppressing inflammation may be helpful for alleviation of mood and cognitive dysfunction observed in GWI.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Anxiety / chemically induced
  • Cell Death
  • Cholinesterase Inhibitors / toxicity
  • DEET / toxicity
  • Depression / chemically induced
  • Disease Models, Animal
  • Hippocampus / drug effects*
  • Hippocampus / pathology
  • Inflammation / chemically induced
  • Insect Repellents / toxicity
  • Insecticides / toxicity
  • Memory Disorders / chemically induced*
  • Memory Disorders / pathology
  • Memory Disorders / physiopathology
  • Mood Disorders / chemically induced*
  • Mood Disorders / pathology
  • Mood Disorders / physiopathology
  • Neurogenesis / drug effects*
  • Neurons / pathology
  • Permethrin / toxicity
  • Persian Gulf Syndrome / chemically induced*
  • Persian Gulf Syndrome / pathology
  • Persian Gulf Syndrome / physiopathology
  • Pyridostigmine Bromide / toxicity
  • Rats
  • Rats, Sprague-Dawley
  • Stress, Psychological / pathology
  • Stress, Psychological / physiopathology*
  • Swimming / psychology

Substances

  • Cholinesterase Inhibitors
  • Insect Repellents
  • Insecticides
  • DEET
  • Permethrin
  • Pyridostigmine Bromide