articleJournal of NeuroscienceMar 1, 2002BRONZE OA

Folic Acid Deficiency and Homocysteine Impair DNA Repair in Hippocampal Neurons and Sensitize Them to Amyloid Toxicity in Experimental Models of Alzheimer's Disease

Center for Neurosciences · National Institute on Aging · +2 more institutions

PubMed
Indexed incrossrefpubmed

Abstract

Recent epidemiological and clinical data suggest that persons with low folic acid levels and elevated homocysteine levels are at increased risk of Alzheimer's disease (AD), but the underlying mechanism is unknown. We tested the hypothesis that impaired one-carbon metabolism resulting from folic acid deficiency and high homocysteine levels promotes accumulation of DNA damage and sensitizes neurons to amyloid beta-peptide (Abeta) toxicity. Incubation of hippocampal cultures in folic acid-deficient medium or in the presence of methotrexate (an inhibitor of folic acid metabolism) or homocysteine induced cell death and rendered neurons vulnerable to death induced by Abeta. Methyl donor deficiency caused uracil…

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645
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FWCI
27.75
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100%
References
83
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Authors

10

Topics & keywords

Keywords
  • Homocysteine
  • Neurodegeneration
  • DNA damage
  • Toxicity
  • Amyloid precursor protein
  • DNA repair
  • Oxidative stress
  • Neurotoxicity
UN Sustainable Development Goals
  • Good health and well-being
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