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Article type: Short Communication
Authors: Cavallaro, Rosaria A.a | Fuso, Andreaa; b | Nicolia, Vincenzinaa; b | Scarpa, Sigfridoa; b; *
Affiliations: [a] Department of Surgery “Pietro Valdoni”, “Sapienza” University of Rome, Rome, Italy | [b] Center for Research in Neurobiology “Daniel Bovet”, “Sapienza” University of Rome, Rome, Italy
Correspondence: [*] Correspondence to: Sigfrido Scarpa, Via A. Scarpa, 14, 00161 Roma, Italy. Tel.: +39 0649766600; Fax: +39 0649766600; E-mail: sigfrido.scarpa@uniroma1.it.
Note: [] Handling Associate Editor: Othman Ghribi
Abstract: Oxidative stress, altered glutathione levels, and hyperhomocysteinemia play critical roles in Alzheimer's disease. We studied the relationships between hyperhomocysteinemia, glutathione, and oxidative stress in TgCRND8 mice maintained in conditions of folate, B12, and B6 deficiency and the effect of S-adenosylmethionine supplementation. We found that hyperhomocysteinemia was correlated with increased reduced/oxidized brain glutathione ratio, with decreased glutathione S-transferase activity and increased lipid peroxidation. S-adenosylmethionine potentiated superoxide dismutase and glutathione S-transferase activity and restored altered brain glutathione and erythrocytes lipid peroxidation. These results underline the importance of S-adenosylmethionine as neuroprotective compound, acting both on methylation and oxidation metabolism.
Keywords: Amyloid-β, glutathione, homocysteine, oxidative stress, S-adenosylmethionine
DOI: 10.3233/JAD-2010-091666
Journal: Journal of Alzheimer's Disease, vol. 20, no. 4, pp. 997-1002, 2010
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