Journal
CURRENT ALZHEIMER RESEARCH
Volume 15, Issue 4, Pages 345-354Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1567205014666170505094549
Keywords
Alzheimer's disease; peroxisome proliferator activated receptors; beta-amyloid; oxidative stress; neuroinflammation; energy metabolism; PEA; fibrates
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Background: The molecular mechanisms underlying Alzheimer's disease (AD) are yet to be fully elucidated. The so-called amyloid cascade hypothesis has long been the prevailing paradigm for causation of disease, and is today being revisited in relation to other pathogenic pathways, such as oxidative stress, neuroinflammation and energy dysmetabolism. The peroxisome proliferator-activated receptors (PPARs) are expressed in the central nervous system (CNS) and regulate many physiological processes, such as energy metabolism, neurotransmission, redox homeostasis, autophagy and cell cycle. Among the three isotypes (alpha, beta/delta, gamma), PPAR gamma role is the most extensively studied, while information on alpha and beta/delta are still scanty. However, recent in vitro and in vivo evidence point to PPAR alpha as a promising therapeutic target in AD. Conclusion: This review provides an update on this topic, focussing on the effects of natural or synthetic agonists in modulating pathogenetic mechanisms at AD onset and during its progression. Ligand-activated PPAR alpha inihibits amyloidogenic pathway, Tau hyperphosphorylation and neuroinflammation. Concomitantly, the receptor elicits an enzymatic antioxidant response to oxidative stress, ameliorates glucose and lipid dysmetabolism, and stimulates autophagy.
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