Glucocorticoid Regulation of GLT-1 Glutamate Transporter Isoform Expression in the Rat Hippocampus

被引:39
|
作者
Autry, Anita E. [1 ]
Grillo, Claudia A. [1 ,3 ]
Piroli, Gerardo G. [1 ,3 ]
Rothstein, Jeffrey D. [2 ]
McEwen, Bruce S. [3 ]
Reagan, Lawrence P. [1 ,3 ]
机构
[1] Univ S Carolina, Sch Med, Dept Pharmacol Physiol & Neurosci, Columbia, SC 29208 USA
[2] Johns Hopkins Univ, Dept Neurol & Neurosci, Baltimore, MD USA
[3] Rockefeller Univ, Harold & Margaret Milliken Hatch Lab Neuroendocri, New York, NY 10021 USA
关键词
Glucocorticoid; Adrenalectomy; Hippocampus; Glutamate; Hybridization; in situ; Radioimmunocytochemistry;
D O I
10.1159/000096092
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In the rat hippocampus, the predominate glutamate transporters are GLT-1 and its recently identified isoform, GLT-1b. Chronic restraint stress increases GLT-1b expression throughout the hippocampus while more selectively increasing GLT-1 expression in the CA3 region. These studies suggest that GLT-1b expression is regulated by stress levels of glucocorticoids (GCs) and GLT-1 expression is regulated by stress-induced increases in extracellular glutamate levels in the CA3 region. Methods: In order to differentiate between the actions of GCs and glutamate, we examined GLT-1 isoform expression in adrenalectomized (ADX) rats and rats exposed to stress levels of GCs. Results: ADX rats revealed no significant differences in GLT-1b mRNA or protein levels compared to sham-operated controls or ADX rats given GC replacement. However, rats exposed to stress levels of GCs exhibited increases in GLT-1b protein expression in the CA3 region and the dentate gyrus. GLT-1 mRNA expression was increased by ADX, increases that were inhibited by GC replacement. Similarly, stress levels of GCs increased GLT-1 protein expression throughout the hippocampus. Conclusions: Taken together, these data indicate that GLT-1b protein expression is regulated by stress levels of GCs while the regulation of GLT-1 mRNA and protein expression provides another example of the biphasic actions of GCs in the central nervous system. Copyright (C) 2006 S. Karger AG, Basel
引用
收藏
页码:371 / 379
页数:9
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