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Article type: Review Article
Authors: Piubelli, Luciano; 1; * | Murtas, Giulia1; | Rabattoni, Valentina | Pollegioni, Loredano
Affiliations: Department of Biotechnology and Life Sciences, University of Insubria, Varese, Italy
Correspondence: [*] Correspondence to: Luciano Piubelli, Department of Biotechnology and Life Sciences, University of Insubria, Via J. H. Dunant 3, 21100 Varese, Italy. Tel.: +39 0332 421 308; Fax: +39 0332 421 500; E-mail: luciano.piubelli@uninsubria.it.
Note: [1] These authors contributed equally to this work.
Abstract: Alzheimer’s disease (AD), the main cause of dementia worldwide, is characterized by a complex and multifactorial etiology. In large part, excitatory neurotransmission in the central nervous system is mediated by glutamate and its receptors are involved in synaptic plasticity. The N-methyl-D-aspartate (NMDA) receptors, which require the agonist glutamate and a coagonist such as glycine or the D-enantiomer of serine for activation, play a main role here. A second D-amino acid, D-aspartate, acts as agonist of NMDA receptors. D-amino acids, present in low amounts in nature and long considered to be of bacterial origin, have distinctive functions in mammals. In recent years, alterations in physiological levels of various D-amino acids have been linked to various pathological states, ranging from chronic kidney disease to neurological disorders. Actually, the level of NMDA receptor signaling must be balanced to promote neuronal survival and prevent neurodegeneration: this signaling in AD is affected mainly by glutamate availability and modulation of the receptor’s functions. Here, we report the experimental findings linking D-serine and D-aspartate, through NMDA receptor modulation, to AD and cognitive functions. Interestingly, AD progression has been also associated with the enzymes related to D-amino acid metabolism as well as with glucose and serine metabolism. Furthermore, the D-serine and D-/total serine ratio in serum have been recently proposed as biomarkers of AD progression. A greater understanding of the role of D-amino acids in excitotoxicity related to the pathogenesis of AD will facilitate novel therapeutic treatments to cure the disease and improve life expectancy.
Keywords: Amyloid-β, D-aspartate, D-serine, excitotoxicity, NMDA receptor
DOI: 10.3233/JAD-201217
Journal: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 475-492, 2021
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