Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6271754 | Neuroscience | 2015 | 16 Pages |
Abstract
A consequence of normal aging is a greater susceptibility to memory impairments following an immune challenge such as infection, surgery, or traumatic brain injury. The neuroinflammatory response, produced by these challenges results in increased and prolonged production of pro-inflammatory cytokines in the otherwise healthy aged brain. Here we discuss the mechanisms by which long-lasting elevations in pro-inflammatory cytokines in the hippocampus produce memory impairments. Sensitized microglia are a primary source of this exaggerated neuroinflammatory response and appear to be a hallmark of the normal aging brain. We review the current understanding of the causes and effects of normal aging-induced microglial sensitization, including dysregulations of the neuroendocrine system, potentiation of neuroinflammatory responses following an immune challenge, and the impairment of memories. We end with a discussion of therapeutic approaches to prevent these deleterious effects.
Keywords
ERKIL-1RACCICD11BIL-1βICMPOCD11β-HSD1NLRP3MHC IITBI11β-hydroxysteroid dehydrogenase type 1LPSIL-6JnkBDNFc-Jun N-terminal kinaseGLT1ROSTraumatic brain injuryIL-1 receptor antagonistMemory impairmentsmajor histocompatibility complex IINeuroinflammationinterleukin-6Interleukin-1 betalong-term potentiationLTPtumor necrosis factor-alphaDanger signalsBrain-derived neurotrophic factorTNF-αlipopolysaccharidemapmitogen-activated proteinExtracellular signal-regulated protein kinaseNormal agingcontrolled cortical impactCORTCorticosteroneGlucocorticoidReactive oxygen speciesComplement receptor 3glucocorticoid receptor
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Authors
R.M. Barrientos, M.M. Kitt, L.R. Watkins, S.F. Maier,