4.6 Review

Impairments in Brain Bioenergetics in Aging and Tau Pathology: A Chicken and Egg Situation?

Journal

CELLS
Volume 10, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/cells10102531

Keywords

tau protein; bioenergetics; brain glucose metabolism; mitochondria; tauopathy; Alzheimer's disease; lifestyle factors; diet; exercise; cognitive stimulation

Categories

Funding

  1. Synapsis Foundation, Alzheimer Research Switzerland [2017-CDA02]
  2. Universitaet Basel Forschungsfonds [3PE1050]

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The brain is the most energy-consuming organ and impairments in brain energy metabolism affect neuronal functionality and viability. There is a link between brain aging and tau pathology, with age-related bioenergetic defects potentially triggering abnormal tau phosphorylation/aggregation and cognitive impairments.
The brain is the most energy-consuming organ of the body and impairments in brain energy metabolism will affect neuronal functionality and viability. Brain aging is marked by defects in energetic metabolism. Abnormal tau protein is a hallmark of tauopathies, including Alzheimer's disease (AD). Pathological tau was shown to induce bioenergetic impairments by affecting mitochondrial function. Although it is now clear that mutations in the tau-coding gene lead to tau pathology, the causes of abnormal tau phosphorylation and aggregation in non-familial tauopathies, such as sporadic AD, remain elusive. Strikingly, both tau pathology and brain hypometabolism correlate with cognitive impairments in AD. The aim of this review is to discuss the link between age-related decrease in brain metabolism and tau pathology. In particular, the following points will be discussed: (i) the common bioenergetic features observed during brain aging and tauopathies; (ii) how age-related bioenergetic defects affect tau pathology; (iii) the influence of lifestyle factors known to modulate brain bioenergetics on tau pathology. The findings compiled here suggest that age-related bioenergetic defects may trigger abnormal tau phosphorylation/aggregation and cognitive impairments after passing a pathological threshold. Understanding the effects of aging on brain metabolism may therefore help to identify disease-modifying strategies against tau-induced neurodegeneration.

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