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Article (Scientific journals)
Molecular mechanisms and therapeutic application of NSAIDs and derived compounds in Alzheimer's disease.
HENEKA, Michael; Kummer, M P; Weggen, S et al.
2011In Current Alzheimer Research, 8 (2), p. 115 - 131
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Keywords :
Anti-Inflammatory Agents, Non-Steroidal; PPAR gamma; Amyloid Precursor Protein Secretases; Alzheimer Disease/drug therapy; Alzheimer Disease/metabolism; Alzheimer Disease/pathology; Amyloid Precursor Protein Secretases/metabolism; Anti-Inflammatory Agents, Non-Steroidal/pharmacology; Blood-Brain Barrier/metabolism; Brain/drug effects; Brain/metabolism; Humans; PPAR gamma/metabolism; ABC transporter; Alzheimer's disease; Amyloid-β; Blood-brain barrier; Clearance; Nonsteroidal anti-inflammatory drug; Nuclear hormone receptor; Peroxisome proliferator activated receptor; Transmembrane receptor; γ-secretase modulation; Neurology; Neurology (clinical)
Abstract :
[en] Alzheimer's disease (AD) is the most common form of neurodegenerative dementias worldwide. Amyloid-β deposition, neurofibrillary tangle formation and Neuroinflammation are the major pathogenetic mechanisms that in concert lead to memory dysfunction and decline of cognition. To date, there is no curative treatment for AD. Epidemiological analysis support the notion that sustained intake of non-steroidal anti-inflammatory drugs (NSAIDs) reduce the risk and delay the onset of AD. In contrast, therapeutic studies testing NSAID efficacy in AD patients have not yielded positive results. This suggests that either the investigated drugs have not addressed the mechanism of action required for mediating beneficial effects or that NSAIDs are effective at stages way before clinical onset of symptoms. The NSAIDs concerned are pleiotrophic in nature and interact with more than one pathomechanism. Therefore evidence for more than one neuroprotective action of NSAIDs has been put forward and it seems likely that some of the drugs act at multiple levels through more than one molecular mechanism. Some, even may not only be beneficial, but negative actions may be overruled by protective effects. Within these mechanisms, modulation of γ-secretase activity, the activation of the peroxisome proliferator-activated receptor-γ, binding to prostaglandin receptors or interactions at the blood-brain barrier may account for the observed protection from AD. This article reviews the current knowledge and views on the above mechanisms and critically discusses current obstacles and the potential as future AD therapeutics.
Disciplines :
Neurology
Author, co-author :
HENEKA, Michael  ;  Department of Neurology, Clinical Neurosciences, Unversity of Bonn, Sigmund-Freud-Str. 25, 53127 Bonn, Germany. michael.heneka@ukb.uni-bonn.de
Kummer, M P;  Clinical Neurosciences, Department of Neurology, Unversity of Bonn, D-53127 Bonn, Germany
Weggen, S;  Molecular Neuropathology Group, Department of Neuropathology, Heinrich-Heine-University, D-40225 Duesseldorf, Germany
Bulic, B;  Research Group Chemical Biology of Neurodegenerative Diseases, Center of Advanced European Studies and Research, D-53175 Bonn, Germany
Multhaup, G;  Institute of Chemistry and Biochemistry, Free University of Berlin, D-14195 Berlin, Germany
Münter, L;  Institute of Chemistry and Biochemistry, Free University of Berlin, D-14195 Berlin, Germany
Hüll, M;  Center of Geriatric Medicine and Gerontology, University of Freiburg, D-79106 Freiburg im Breisgau, Germany
Pflanzner, T;  Institute of Pathobiochemistry, Molecular Neurodegeneration, University Medical Center of the Johannes Gutenberg University Mainz, 55099 Mainz, Germany
Pietrzik, C U;  Institute of Pathobiochemistry, Molecular Neurodegeneration, University Medical Center of the Johannes Gutenberg University Mainz, 55099 Mainz, Germany
External co-authors :
yes
Language :
English
Title :
Molecular mechanisms and therapeutic application of NSAIDs and derived compounds in Alzheimer's disease.
Publication date :
March 2011
Journal title :
Current Alzheimer Research
ISSN :
1567-2050
Publisher :
Bentham Science Publishers, United Arab Emirates
Volume :
8
Issue :
2
Pages :
115 - 131
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBilu :
since 07 May 2024

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