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乙醇和尼古丁对海马钙结合蛋白-D28k表达的相反作用。

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

作者信息

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

机构信息

Department of Psychology, University of Kentucky, 115 Kastle Hall, Lexington, KY 40506-0044, USA.

出版信息

Alcohol. 2003 Aug-Oct;31(1-2):1-10. doi: 10.1016/j.alcohol.2003.09.001.

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.

摘要

长期接触乙醇会产生多种神经适应性变化,这可能导致乙醇戒断期间钙(Ca(2+))平衡失调和神经毒性。相反,接触尼古丁可能会减轻钙(Ca(2+))失调的神经毒性后果,推测是通过上调钙缓冲蛋白钙结合蛋白-D(28k)来实现的。当前的研究旨在探究10天的乙醇暴露和戒断对大鼠海马体中钙结合蛋白-D(28k)表达的影响程度。此外,在这些研究中,我们研究了尼古丁通过作用于含α(7)*的烟碱型乙酰胆碱受体(nAChRs)来拮抗乙醇暴露对钙结合蛋白-D(28k)表达的影响的能力。将大鼠海马体的器官型培养物暴露于乙醇(50 - 100 mM)中10天。另外的培养物暴露于500 nM(-)-尼古丁,同时添加或不添加50 mM乙醇、100 nM甲基lycaconitine(一种含α(7)的nAChR拮抗剂)或两者。长期暴露于乙醇(≥50 mM)会导致海马结构所有区域的钙结合蛋白-D(28k)免疫标记显著减少,即使在无毒浓度的乙醇环境下也是如此。从10天的乙醇暴露中戒断72小时后,钙结合蛋白-D(28k)表达水平恢复到接近对照水平。长期暴露于(-)-尼古丁会使钙结合蛋白-D(28k)表达水平显著升高,而与甲基lycaconitine共同暴露可阻止这种升高。培养物同时暴露于(-)-尼古丁和乙醇会减轻乙醇诱导的钙结合蛋白-D(28k)表达水平降低。这些发现支持了以下观点:长期乙醇暴露以可逆方式降低了神经元缓冲积累钙(Ca(2+))的能力,这种效应可能导致戒断诱导的神经毒性。此外,长期暴露于(-)-尼古丁以α(7) nAChR依赖的方式增强钙结合蛋白-D(28k)表达,并拮抗乙醇对钙结合蛋白-D(28k)表达的影响。

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