Acamprosate, MK-801, and ifenprodil inhibit neurotoxicity and calcium entry induced by ethanol withdrawal in organotypic slice cultures from neonatal rat hippocampus.
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Abstract |
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The antirelapse drug acamprosate has previously been reported to inhibit activating effects of polyamines on -methyl-D-aspartic acid receptor (NMDAR) function. Because increased synthesis of polyamines has been suggested as a mechanism for potentiation of NMDAR function during ethanol withdrawal, we evaluated the effects of acamprosate, MK-801, and ifenprodil in a cell culture model of ethanol withdrawal-induced neurotoxicity. |
Year of Publication |
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2002
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Journal |
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Alcoholism, clinical and experimental research
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Volume |
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26
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Issue |
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10
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Number of Pages |
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1468-78
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ISSN Number |
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0145-6008
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DOI |
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10.1097/01.ALC.0000033261.14548.D2
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Short Title |
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Alcohol Clin Exp Res
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