Literature DB >> 1755879

Brain aging and Alzheimer's disease, "wear and tear" versus "use it or lose it".

D F Swaab1.   

Abstract

In organs other than the brain, cell activation seems to increase "wear and tear," e.g., by increased free-radical formation, and so to cause an increased rate of aging. However, activation of nerve cells within the physiological range seems to lead to maintenance of neurons during aging and in Alzheimer's disease, possibly by preferentially stimulating the action of protective mechanisms such as DNA repair. This "use it or lose it" principle might explain why certain neurons degenerate in aging or Alzheimer's disease while others do not, and why recovery of various neuronal systems during aging has been obtained by restoration of the missing stimulus. Consequently, neuronal activation might provide a means of prolonging its optimal function for the full length of our natural life span.

Entities:  

Mesh:

Year:  1991        PMID: 1755879     DOI: 10.1016/0197-4580(91)90008-8

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   4.673


  25 in total

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5.  Axonal tract tracing for delineating interacting brain regions: implications for Alzheimer's disease-associated memory.

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6.  Education and dementia.

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8.  A life course model of cognitive activities, socioeconomic status, education, reading ability, and cognition.

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9.  Neurotrophin receptor p75 mediates the uptake of the amyloid beta (Aβ) peptide, guiding it to lysosomes for degradation in basal forebrain cholinergic neurons.

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Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-06       Impact factor: 11.205

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