Abstract
Cortical cells from embryonic mice (E17) showed a rapid cell-death under the serum-free condition. The addition of nefiracetam at 0.1-10 microM increased the survival activity, while aniracetam at the same concentrations did not. The cell death was characterized to be apoptotic, since dead cells showed nuclear condensation, fragmentation, and TUNEL-positive staining. The nefiracetam-induced anti-apoptotic activity was completely blocked by 1 microM nifedipine or omega-conotoxin GVIA, and partially by 1 microM verapamil. These results suggest that the reported anti-amnesic action of nefiracetam in ischemic animals may be partly attributed to the neuroprotective action.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Apoptosis / drug effects*
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Apoptosis / physiology
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Brain-Derived Neurotrophic Factor / pharmacology*
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Cell Death / drug effects*
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Cell Survival / drug effects*
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Cells, Cultured
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Cerebral Cortex / cytology*
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Cerebral Cortex / embryology
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Cognition / drug effects
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Cognition / physiology
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Culture Media, Serum-Free
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Embryo, Mammalian
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In Situ Nick-End Labeling
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Mice
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Mice, Inbred Strains
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Neurons / cytology*
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Neurons / drug effects
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Nootropic Agents / pharmacology*
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Pyrrolidinones / pharmacology*
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Verapamil / pharmacology
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omega-Conotoxin GVIA / pharmacology
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omega-Conotoxins / pharmacology
Substances
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Brain-Derived Neurotrophic Factor
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Culture Media, Serum-Free
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Nootropic Agents
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Pyrrolidinones
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omega-Conotoxins
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nefiracetam
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omega-Conotoxin GVIA
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Verapamil