4.7 Article

Melatonin improves brain function in a model of chronic Gulf War Illness with modulation of oxidative stress, NLRP3 inflammasomes, and BDNF-ERK-CREB pathway in the hippocampus

期刊

REDOX BIOLOGY
卷 43, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.redox.2021.101973

关键词

Brain-derived neurotrophic factor; cAMP response element-binding protein; Cognitive and mood function; Inflammasomes; Mitochondria; Neuroinflammation; Neurogenesis; Oxidative stress

资金

  1. Department of Defense (GWIRP grants) [W81XWH-17-1-0447, W81XWH-16-1-0480]
  2. National Institutes of Health [R01NS106907-01]

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The study showed that melatonin can improve cognitive and mood function in rats with chronic Gulf War Illness, with higher doses having a better effect. The improvement is mainly achieved through antioxidant and anti-inflammatory effects to alleviate neuroinflammation and mood disorders.
Persistent cognitive and mood dysfunction is the primary CNS symptom in veterans afflicted with Gulf War Illness (GWI). This study investigated the efficacy of melatonin (MEL) for improving cognitive and mood function with antioxidant, antiinflammatory, and pro-cognitive effects in a rat model of chronic GWI. Six months after exposure to GWI-related chemicals and stress, rats were treated with vehicle or MEL (5, 10, 20, 40, and 80 mg/ kg) for eight weeks. Behavioral tests revealed cognitive and mood dysfunction in GWI rats receiving vehicle, which were associated with elevated oxidative stress, reduced NRF2, catalase and mitochondrial complex proteins, astrocyte hypertrophy, activated microglia with NLRP3 inflammasomes, elevated proinflammatory cytokines, waned neurogenesis, and synapse loss in the hippocampus. MEL at 10 mg/kg alleviated simple and associative recognition memory dysfunction and anhedonia, along with reduced oxidative stress, enhanced glutathione and complex III, and reduced NLRP3 inflammasomes, IL-18, TNF-alpha, and IFN-gamma. MEL at 20 mg/kg also normalized NRF2 and catalase and increased microglial ramification. MEL at 40 mg/kg, in addition, reduced astrocyte hypertrophy, activated microglia, NF-kB-NLRP3-caspase-1 signaling, IL-1 beta, MCP-1, and MIP-1 alpha. Moreover, MEL at 80 mg/kg activated the BDNF-ERK-CREB signaling pathway, enhanced neurogenesis and diminished synapse loss in the hippocampus, and improved a more complex hippocampus-dependent cognitive function. Thus, MEL therapy is efficacious for improving cognitive and mood function in a rat model of chronic GWI, and MEL's effect was dose-dependent. The study provides the first evidence of MEL's promise for alleviating neuroinflammation and cognitive and mood impairments in veterans with chronic GWI.

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