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  Glycation in Parkinson's disease and Alzheimer's disease

Miranda, H. V., El-Agnaf, O. M. A., & Outeiro, T. F. (2016). Glycation in Parkinson's disease and Alzheimer's disease. Movement Disorders, 31(6), 782-790. doi:10.1002/mds.26566.

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Movement Disorders - 2016 - Vicente Miranda.pdf (Publisher version), 504KB
 
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Movement Disorders - 2016 - Vicente Miranda.pdf
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2016-03-04
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 Creators:
Miranda, Hugo Vicente, Author
El-Agnaf, Omar M. A., Author
Outeiro, Tiago F.1, Author           
Affiliations:
1Experimental Neurodegeneration, Max Planck Institute of Experimental Medicine, Max Planck Society, ou_3398149              

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Free keywords: Glycation; Neurodegenerative diseases; Alzheimer's disease; Parkinson's disease
 Abstract: Glycation is a spontaneous age-dependent posttranslational modification that can impact the structure and function of several proteins. Interestingly, glycation can be detected at the periphery of Lewy bodies in the brain in Parkinson's disease. Moreover, α-synuclein can be glycated, at least under experimental conditions. In Alzheimer's disease, glycation of amyloid β peptide exacerbates its toxicity and contributes to neurodegeneration. Recent studies establish diabetes mellitus as a risk factor for several neurodegenerative disorders, including Parkinson's and Alzheimer's diseases. However, the mechanisms underlying this connection remain unclear. We hypothesize that hyperglycemia might play an important role in the development of these disorders, possibly by also inducing protein glycation and thereby dysfunction, aggregation, and deposition. Here, we explore protein glycation as a common player in Parkinson's and Alzheimer's diseases and propose it may constitute a novel target for the development of strategies for neuroprotective therapeutic interventions. © 2016 International Parkinson and Movement Disorder Society

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Language(s): eng - English
 Dates: 2016-03-042016-06
 Publication Status: Issued
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/mds.26566
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Title: Movement Disorders
Source Genre: Journal
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Publ. Info: New York, NY : John Wiley & Sons
Pages: - Volume / Issue: 31 (6) Sequence Number: - Start / End Page: 782 - 790 Identifier: ISSN: 0885-3185
CoNE: https://pure.mpg.de/cone/journals/resource/954925551353