Neuroinflammation: A Potential Risk for Dementia.
Md Afroz AhmadOzaifa KareemMohammad KhushtarMd AkbarMd Rafiul HaqueAshif IqubalMd Faheem HaiderFaheem Hyder PottooFatima S AbdullaMahia B Al-HaidarNoora AlhajriPublished in: International journal of molecular sciences (2022)
Dementia is a neurodegenerative condition that is considered a major factor contributing to cognitive decline that reduces independent function. Pathophysiological pathways are not well defined for neurodegenerative diseases such as dementia; however, published evidence has shown the role of numerous inflammatory processes in the brain contributing toward their pathology. Microglia of the central nervous system (CNS) are the principal components of the brain's immune defence system and can detect harmful or external pathogens. When stimulated, the cells trigger neuroinflammatory responses by releasing proinflammatory chemokines, cytokines, reactive oxygen species, and nitrogen species in order to preserve the cell's microenvironment. These proinflammatory markers include cytokines such as IL-1, IL-6, and TNFα chemokines such as CCR3 and CCL2 and CCR5. Microglial cells may produce a prolonged inflammatory response that, in some circumstances, is indicated in the promotion of neurodegenerative diseases. The present review is focused on the involvement of microglial cell activation throughout neurodegenerative conditions and the link between neuroinflammatory processes and dementia.
Keyphrases
- mild cognitive impairment
- cognitive decline
- inflammatory response
- lipopolysaccharide induced
- cognitive impairment
- induced apoptosis
- lps induced
- reactive oxygen species
- cell cycle arrest
- single cell
- stem cells
- dendritic cells
- rheumatoid arthritis
- cell therapy
- cerebral ischemia
- traumatic brain injury
- resting state
- endoplasmic reticulum stress
- systematic review
- spinal cord injury
- regulatory t cells
- randomized controlled trial
- blood brain barrier
- signaling pathway
- cell death
- multiple sclerosis
- immune response
- spinal cord
- cerebrospinal fluid
- risk assessment
- subarachnoid hemorrhage
- mesenchymal stem cells
- amino acid
- gram negative
- meta analyses