Current Neuropharmacology

T.E. Salt
University College London
Institute of Ophthalmology
London EC1V 9EL


Impact and Therapeutic Potential of PPARs in Alzheimers Disease

Author(s): Michael T. Heneka, Elisabet Reyes-Irisarri, Michael Hull and Markus P. Kummer

Affiliation: University of Bonn, Department of Neurology, Clinical Neurosciences, Bonn, Germany.

Keywords: Neuroinflammation, alzheimer's disease, thiazolidinediones, PPAR, Therapeutic Potential, activated receptors (PPARs), Non-steroidal anti-inflammatory drugs, PPAR activation, retinoid-X-receptors (RXRs)


Peroxisome proliferator activated receptors (PPARs) are well studied for their role of peripheral metabolism, but they also may be involved in the pathogenesis of various disorders of the central nervous system (CNS) including multiple sclerosis, amyotrophic lateral sclerosis, Alzheimers and, Parkinsons disease. The observation that PPARs are able to suppress the inflammatory response in peripheral macrophages and in several models of human autoimmune diseases, lead to the idea that PPARs might be beneficial for CNS disorders possessing an inflammatory component. The neuroinflammatory response during the course of Alzheimers disease (AD) is triggered by the deposition of the β-amyloid peptide in extracellular plaques and ongoing neurodegeneration. Non-steroidal anti-inflammatory drugs (NSAIDs) have been considered to delay the onset and reduce the risk to develop Alzheimers disease, while they also directly activate PPARγ. This led to the hypothesis that NSAID protection in AD may be partly mediated by PPARγ. Several lines of evidence have supported this hypothesis, using AD related transgenic cellular and animal models. Stimulation of PPARγ by synthetic agonist (thiazolidinediones) inducing anti-inflammatory, anti-amyloidogenic and insulin sensitizing effects may account for the observed effects. Several clinical trials already revealed promising results using PPARγ agonists, therefore PPARγ represents an attractive therapeutic target for the treatment of AD.

Order Reprints Order Eprints Rights & PermissionsPrintExport

Article Details

Page: [643 - 650]
Pages: 8
DOI: 10.2174/157015911798376325