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      Homocysteine elicits a DNA damage response in neurons that promotes apoptosis and hypersensitivity to excitotoxicity.

      The Journal of neuroscience : the official journal of the Society for Neuroscience
      Animals, Apoptosis, physiology, Benzamides, pharmacology, Calcium, metabolism, Cells, Cultured, DNA, drug effects, DNA Damage, Egtazic Acid, analogs & derivatives, Enzyme Inhibitors, Excitatory Amino Acid Agonists, Hippocampus, cytology, Homocysteine, Intracellular Fluid, Kainic Acid, Membrane Potentials, Mitochondria, NAD, Neurons, Poly(ADP-ribose) Polymerases, antagonists & inhibitors, Rats, Tumor Suppressor Protein p53

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          Abstract

          Elevated plasma levels of the sulfur-containing amino acid homocysteine increase the risk for atherosclerosis, stroke, and possibly Alzheimer's disease, but the underlying mechanisms are unknown. We now report that homocysteine induces apoptosis in rat hippocampal neurons. DNA strand breaks and associated activation of poly-ADP-ribose polymerase (PARP) and NAD depletion occur rapidly after exposure to homocysteine and precede mitochondrial dysfunction, oxidative stress, and caspase activation. The PARP inhibitor 3-aminobenzamide (3AB) protects neurons against homocysteine-induced NAD depletion, loss of mitochondrial transmembrane potential, and cell death, demonstrating a requirement for PARP activation and/or NAD depletion in homocysteine-induced apoptosis. Caspase inhibition accelerates the loss of mitochondrial potential and shifts the mode of cell death to necrosis; inhibition of PARP with 3AB attenuates this effect of caspase inhibition. Homocysteine markedly increases the vulnerability of hippocampal neurons to excitotoxic and oxidative injury in cell culture and in vivo, suggesting a mechanism by which homocysteine may contribute to the pathogenesis of neurodegenerative disorders.

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