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Gulf War Illness: Mechanisms Underlying Brain Dysfunction and Promising Therapeutic Strategies

Journal

PHARMACOLOGY & THERAPEUTICS
Volume 220, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pharmthera.2020.107716

Keywords

Chemical exposures; Cognitive dysfunction; Coenzyme Q10; Curcumin; DNA methylation; Depression; Microbiota; Mitochondrial dysfunction; Neuroinflammation; Oxidative Stress

Funding

  1. Department of Defense [W81XWH-14-1-0572, W81XWH-16-1-0480, W81XWH-17-1-0447]
  2. National Institutes of Health - National Institute of Neurological Disorders and Stroke [NIH-NINDS R01NS106907-01]
  3. Texas A&M College of Medicine

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Gulf War Illness (GWI) is a chronic multisymptom health problem affecting about 30% of veterans from the first Gulf War. Impaired brain function is a significant symptom of GWI, with studies in both animal models and veterans pointing to mechanisms such as oxidative stress, inflammation, altered lipid metabolism, and mitochondrial dysfunction. Promising therapeutic strategies are being explored, including antioxidants and anti-inflammatory compounds, although more research is needed to validate these findings.
Gulf War Illness (GWI), a chronic multisymptom health problem, afflicts similar to 30% of veterans served in the first GW. Impaired brain function is among the most significant symptoms of GWI, which is typified by persistent cognitive and mood impairments, concentration problems, headaches, chronic fatigue, and musculoskeletal pain. This review aims to discuss findings from animal prototypes and veterans with GWI on mechanisms underlying its pathophysiology and emerging therapeutic strategies for alleviating brain dysfunction in GWI. Animal model studies have linked brain impairments to incessantly elevated oxidative stress, chronic inflammation, inhibitory interneuron loss, altered lipid metabolism and peroxisomes, mitochondrial dysfunction, modified expression of genes relevant to cognitive function, and waned hippocampal neurogenesis. Furthermore, the involvement of systemic alterations such as the increased intensity of reactive oxygen species and proinflammatory cytokines in the blood, transformed gut microbiome, and activation of the adaptive immune response have received consideration. Investigations in veterans have suggested that brain dysfunction in GWI is linked to chronic activation of the executive control network, impaired functional connectivity, altered blood flow, persistent inflammation, and changes in miRNA levels. Lack of protective alleles from Class II HLA genes, the altered concentration of phospholipid species and proinflammatory factors in the circulating blood have also been suggested as other aiding factors. While some drugs or combination therapies have shown promise for alleviating symptoms in clinical trials, larger double-blind, placebo-controlled trials are needed to validate such findings. Based on improvements seen in animal models of GWI, several antioxidants and anti-inflammatory compounds are currently being tested in clinical trials. However, reliable blood biomarkers that facilitate an appropriate screening of veterans for brain pathology need to be discovered. A liquid biopsy approach involving analysis of brain-derived extracellular vesicles in the blood appears efficient for discerning the extent of neuropathology both before and during clinical trials. Published by Elsevier Inc.

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