Neural mechanisms of ageing and cognitive decline
By Nicholas A. Bishop, Tao Lu, B. Yankner. Nature, 2010
1,288 citations recorded by the source corpus.
During the past century, treatments for the diseases of youth and middle age have helped raise life expectancy significantly. However, cognitive decline has emerged as one of the greatest health threats of old age, with nearly 50% of adults over the age of 85 afflicted with Alzheimer's disease. Developing therapeutic interventions for such conditions demands a greater understanding of the processes underlying normal and pathological brain ageing. Recent advances in the biology of ageing in model organisms, together with molecular and systems-level studies of the brain, are beginning to shed light on these mechanisms and their potential roles in cognitive decline.
Subfields: Aging, Molecular Biology, Physiology
View Paper: https://www.semanticscholar.org/paper/a19204eb07fad92d7cad4384ad1718389537de4e
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Citations in the corpus
- Ageing as a risk factor for disease. (2012, background): “Transcription of genes encoding mitochondrial proteins declines with age [42], and impaired mitochondrial fission leads to disorganized mitochondrial morphology [61].”
- Decoding Alzheimer's disease from perturbed cerebral glucose metabolism: implications for diagnostic and therapeutic strategies. (2013, background): “Under genetic background and pathophysiological condition of AD, oxidative stress and this vicious circle are more prone to take place and have been demonstrated as an early event occurring before the appearance of senile plaques and onset of clinical manifestations (Bishop et al., 2010; Bonilla et ”
- Fasting: Molecular Mechanisms and Clinical Applications (2014, background): “Major factors implicated in aging whose generation are accelerated by gluttonous lifestyles and slowed by energy restriction in humans include the following: (1) oxidative damage to proteins, DNA, and lipids; (2) inflammation; (3) accumulation of dysfunctional proteins and organelles; and (4) elevat”
- SIRTUIN 1 AND SIRTUIN 3: PHYSIOLOGICAL MODULATORS OF METABOLISM (2012, background): “Moreover, Sir2 has no effect on yeast survival under starvation (97) or in worms under CR (41).”