Could Alcohol-Related Cognitive Decline Be the Result of Iron-Induced Neuroinflammation?
Thomas D W WilcocksonSankanika RoyPublished in: Brain sciences (2024)
Excessive and prolonged alcohol use can have long-term severe neurological consequences. The mechanisms involved may be complicated; however, new evidence seems to indicate the involvement of iron accumulation and neuroinflammation. Prolonged alcohol consumption has been linked to the accumulation of iron in specific regions of the brain. Evidence suggests that excess iron in the brain can trigger microglia activation in response. This activation leads to the release of pro-inflammatory cytokines and reactive oxygen species, which can cause damage to neurons and surrounding brain tissue. Additionally, iron-induced oxidative stress and inflammation can disrupt the blood-brain barrier, allowing immune cells from the periphery to infiltrate the brain. This infiltration can lead to further neuroinflammatory responses. Inflammation in the brain subsequently disrupts neuronal networks, impairs synaptic plasticity, and accelerates neuronal cell death. Consequently, cognitive functions such as memory, attention, and decision-making are compromised. Additionally, chronic neuroinflammation can hasten the development and progression of neurodegenerative diseases, further exacerbating cognitive impairment. Therefore, alcohol could act as a trigger for iron-induced neuroinflammation and cognitive decline. Overall, the mechanisms at play here seem to strongly link alcohol with cognitive decline, with neuroinflammation resulting from alcohol-induced iron accumulation playing a pivotal role.
Keyphrases
- cognitive decline
- cerebral ischemia
- alcohol consumption
- cognitive impairment
- mild cognitive impairment
- iron deficiency
- resting state
- subarachnoid hemorrhage
- white matter
- lipopolysaccharide induced
- traumatic brain injury
- blood brain barrier
- oxidative stress
- cell death
- diabetic rats
- lps induced
- brain injury
- high glucose
- drug induced
- reactive oxygen species
- inflammatory response
- functional connectivity
- multiple sclerosis
- signaling pathway
- early onset
- hydrogen peroxide
- body mass index
- cell proliferation