regulation of kainate receptor subunit mrna by stress and corticosteroids in the rat hippocampuskainate监管压力和糖皮质激素受体亚基mrna的鼠海马.pdfVIP
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regulation of kainate receptor subunit mrna by stress and corticosteroids in the rat hippocampuskainate监管压力和糖皮质激素受体亚基mrna的鼠海马
Regulation of Kainate Receptor Subunit mRNA by Stress
and Corticosteroids in the Rat Hippocampus
Richard G. Hunter*, Rudy Bellani, Erik Bloss, Ana Costa, Katharine McCarthy, Bruce S. McEwen
Laboratory of Neuroendocrinology, The Rockefeller University, New York, New York, United States of America
Abstract
Kainate receptors are a class of ionotropic glutamate receptors that have a role in the modulation of glutamate release and
synaptic plasticity in the hippocampal formation. Previous studies have implicated corticosteroids in the regulation of these
receptors and recent clinical work has shown that polymorphisms in kainate receptor subunit genes are associated with
susceptibility to major depression and response to anti-depressant treatment. In the present study we sought to examine
the effects of chronic stress and corticosteroid treatments upon the expression of the mRNA of kainate receptor subunits
GluR5-7 and KA1-2. Our results show that, after 7 days, adrenalectomy results in increased expression of hippocampal KA1,
GluR6 and GluR7 mRNAs, an effect which is reversed by treatment with corticosterone in the case of KA1 and GluR7 and by
aldosterone treatment in the case of GluR6. 21 days of chronic restraint stress (CRS) elevated the expression of the KA1
subunit, but had no effect on the expression of the other subunits. Similarly, 21 days of treatment with a moderate dose of
corticosterone also increased KA1 mRNA in the dentate gyrus, whereas a high corticosterone dose has no effect. Our results
suggest an interaction between hippocampal kainate receptor composition and the hypothalamic-pituitary-adrenal (HPA)
axis and show a selective chronic stress induced modulation of the KA1 subunit in the dentate gyrus and CA3 that has
implications for stress-induced adaptive structural plasticity.
Citation: Hunter RG, Bellani R, Bloss E, Costa A, McCarthy K, et al. (2009) Regulati
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