Literature DB >> 10822141

Prenatal and postnatal exposure to ethanol induces changes in the shape of the dendritic spines from hippocampal CA1 pyramidal neurons of the rat.

L Tarelo-Acuña1, E Olvera-Cortés, I González-Burgos.   

Abstract

20%-ethanol was provided to adult female rats since a pregestational stage until weaning of the pups, and percentage proportion of thin, mushroom-shaped, stubby, or wide spines from the apical dendrite of hippocampal CA1 pyramidal cells, was counted at 15, 21, 40, and 90 days of age. By-kind-of-spine analysis revealed higher fluctuation of experimental spines, and less percentage of thin spines was observed in the ethanol-intoxicated rats concomitantly with a higher proportion of stubby or wide spines; through development. Because thin spines may propagate the synaptic potentials more efficiently than stubby or wide spines, this findings suggest that the electrical excitability and thereafter the firing pattern of those cells may be altered, due to the toxic effects of chronic ethanol ingestion.

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Year:  2000        PMID: 10822141     DOI: 10.1016/s0304-3940(00)01075-2

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  18 in total

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Review 4.  Neurochemical and neurostructural plasticity in alcoholism.

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5.  The Impact of Prenatal Ethanol Exposure on Neuroanatomical and Behavioral Development in Mice.

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Journal:  Alcohol Clin Exp Res       Date:  2016-01       Impact factor: 3.455

6.  Alcohol exposure during development: Impact on the epigenome.

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7.  Chronic alcohol alters dendritic spine development in neurons in primary culture.

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Review 8.  New insights on neurobiological mechanisms underlying alcohol addiction.

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9.  Transgenic expression of Glud1 (glutamate dehydrogenase 1) in neurons: in vivo model of enhanced glutamate release, altered synaptic plasticity, and selective neuronal vulnerability.

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10.  Pre-administration of G9a/GLP inhibitor during synaptogenesis prevents postnatal ethanol-induced LTP deficits and neurobehavioral abnormalities in adult mice.

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