Literature DB >> 14615005

Opposing effects of ethanol and nicotine on hippocampal calbindin-D28k expression.

Patrick J Mulholland1, Barton R Harris, Lincoln H Wilkins, Rachel L Self, John A Blanchard, Robert C Holley, John M Littleton, Mark A Prendergast.   

Abstract

Long-term ethanol exposure produces multiple neuroadaptations that likely contribute to dysregulation of Ca(2+) balance and neurotoxicity during ethanol withdrawal. Conversely, nicotine exposure may reduce the neurotoxic consequences of Ca(2+) dysregulation, putatively through up-regulation of the Ca(2+)-buffering protein calbindin-D(28k). The current studies were designed to examine the extent to which 10-day ethanol exposure and withdrawal altered calbindin-D(28k) expression in rat hippocampus. Further, in these studies, we examined the ability of nicotine, through action at alpha(7)(*)-bearing nicotinic acetylcholine receptors (nAChRs), to antagonize the effects of ethanol exposure on calbindin-D(28k) expression. Organotypic cultures of rat hippocampus were exposed to ethanol (50-100 mM) for 10 days. Additional cultures were exposed to 500 nM (-)-nicotine with or without the addition of 50 mM ethanol, 100 nM methyllycaconitine (an alpha(7)*-bearing nAChR antagonist), or both. Prolonged exposure to ethanol (>/=50 mM) produced significant reductions of calbindin-D(28k) immunolabeling in all regions of the hippocampal formation, even at nontoxic concentrations of ethanol. Calbindin-D(28k) expression levels returned to near-control levels after 72 h of withdrawal from 10-day ethanol exposure. Extended (-)-nicotine exposure produced significant elevations in calbindin-D(28k) expression levels that were prevented by methyllycaconitine co-exposure. Co-exposure of cultures to (-)-nicotine with ethanol resulted in an attenuation of ethanol-induced reductions in calbindin-D(28k) expression levels. These findings support the suggestion that long-term ethanol exposure reduces the neuronal capacity to buffer accumulated Ca(2+) in a reversible manner, an effect that likely contributes to withdrawal-induced neurotoxicity. Further, long-term exposure to (-)-nicotine enhances calbindin-D(28k) expression in an alpha(7)* nAChR-dependent manner and antagonizes the effects of ethanol on calbindin-D(28k) expression.

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Year:  2003        PMID: 14615005     DOI: 10.1016/j.alcohol.2003.09.001

Source DB:  PubMed          Journal:  Alcohol        ISSN: 0741-8329            Impact factor:   2.405


  4 in total

1.  Loss of calcium and increased apoptosis within the same neuron.

Authors:  C P Turner; J Connell; K Blackstone; S L Ringler
Journal:  Brain Res       Date:  2006-11-22       Impact factor: 3.252

2.  Inositol 1,4,5 trisphosphate receptor and chromogranin B are concentrated in different regions of the hippocampus.

Authors:  Nils H Nicolay; Daniel Hertle; Wolfgang Boehmerle; Felix M Heidrich; Mark Yeckel; Barbara E Ehrlich
Journal:  J Neurosci Res       Date:  2007-07       Impact factor: 4.164

3.  A Novel Sulfonamide, 4-FS, Reduces Ethanol Drinking and Physical Withdrawal Associated With Ethanol Dependence.

Authors:  Muhammad Sona Khan; Wulfran Trenet; Nancy Xing; Britta Sibley; Muzaffar Abbas; Mariya Al-Rashida; Khalid Rauf; Chitra D Mandyam
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4.  The Interplay between the Hippocampus and Amygdala in Regulating Aberrant Hippocampal Neurogenesis during Protracted Abstinence from Alcohol Dependence.

Authors:  Chitra D Mandyam
Journal:  Front Psychiatry       Date:  2013-06-27       Impact factor: 4.157

  4 in total

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