Aging brain

Aging of the brain is a process of transformation of the brain in older age, including changes all individuals experience and those of illness (including unrecognised illness). Usually this refers to humans.

Since life extension is only pertinent if accompanied by health span extension, and, more importantly, by preserving brain health and cognition, finding rejuvenating approaches that act simultaneously in peripheral tissues and in brain function is a key strategy for development of rejuvenating technology.[1]

Aging is a major risk factor for most common neurodegenerative diseases, including mild cognitive impairment, dementias including Alzheimer's disease, cerebrovascular disease, Parkinson's disease, and Lou Gehrig's disease.[2][3] While much research has focused on diseases of aging, there are few informative studies on the molecular biology of the aging brain (usually spelled ageing brain in British English) in the absence of neurodegenerative disease or the neuropsychological profile of healthy older adults. However, research suggests that the aging process is associated with several structural, chemical, and functional changes in the brain as well as a host of neurocognitive changes. Recent reports in model organisms suggest that as organisms age, there are distinct changes in the expression of genes at the single neuron level.[4] This page is an overview of the changes associated with human brain aging, including aging without concomitant diseases.

  1. ^ Gaspar-Silva, Filipa; Trigo, Diogo; Magalhaes, Joana (24 June 2023). "Ageing in the brain: mechanisms and rejuvenating strategies". Cellular and Molecular Life Sciences. 80 (7): 190. doi:10.1007/s00018-023-04832-6. PMC 10290611. PMID 37354261.
  2. ^ Cummings, Jeffrey L. (2002-05-08). "Alzheimer Disease". JAMA. 287 (18): 2335–2338. doi:10.1001/jama.287.18.2335. ISSN 0098-7484. PMID 11988038.
  3. ^ Winder, Nick R.; Reeve, Emily H.; Walker, Ashley E. (2021-01-01). "Large artery stiffness and brain health: insights from animal models". American Journal of Physiology. Heart and Circulatory Physiology. 320 (1): H424–H431. doi:10.1152/ajpheart.00696.2020. ISSN 0363-6135. PMC 7847068. PMID 33164578.
  4. ^ Kadakkuzha, Beena M; Akhmedov, Komolitdin (2013-12-14). "Age-associated bidirectional modulation of gene expression in single identified R15 neuron of Aplysia". BMC Genomics. 14 (1): 880. doi:10.1186/1471-2164-14-880. PMC 3909179. PMID 24330282.

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