4.5 Article

Glucocorticoid status affects antidepressant regulation of locus coeruleus tyrosine hydroxylase and dorsal raphe tryptophan hydroxylase gene expression

期刊

BRAIN RESEARCH
卷 1288, 期 -, 页码 69-78

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ELSEVIER
DOI: 10.1016/j.brainres.2009.06.082

关键词

Glucocorticoid; Tricyclic antidepressant; Monoamine oxidase inhibitor; HPA axis; Glucocorticoid receptor; Mineralocorticoid receptor; Norepinephrine; Serotonin

资金

  1. National Alliance for Research on Schizophrenia and Depression (NARSAD)
  2. Albany Medical College [RO1 MH80394]

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Brainstem monoaminergic nuclei express glucocorticoid receptors (GR), and glucocorticoids have been shown to inhibit expression of enzymes involved in monoamine synthesis. Monoamine deficits have been implicated in depression pathology. However, it is unknown if antidepressants regulate brainstem GR, and if glucocorticoids might influence antidepressant effects on monoamine-synthesizing enzymes. Our lab has found opposing effects of the monoamine oxidase inhibitor phenelzine and the tricyclic antidepressant imipramine on HPA activity and forebrain GR gene expression. We therefore hypothesized that phenelzine and imipramine would also affect brainstem GR gene expression differentially, and that antidepressant-induced changes in GR expression would correlate with effects on monoamine-synthesizing enzyme expression. Using in situ hybridization, we measured effects of chronic antidepressant treatment on brainstem GR, locus coeruleus and ventral tegmental area (VTA) tyrosine hydroxylase (TH), and dorsal raphe tryptophan hydroxylase (TPH2) gene expression in male CS7BL/6 mice that were adrenalectomized and replaced with defined levels of corticosterone. GR expression was decreased by phenelzine in the locus coeruleus and decreased by imipramine in the dorsal raphe. Phenelzine increased locus coeruleus TH and imipramine increased dorsal raphe TPH2 gene expression in a glucocorticoid-dependent manner, suggesting that increases in these enzymes were due to relief of inhibitory glucocorticoid signaling. We did not find antidepressant effects on GR or TH expression in the VTA or on mineralocorticoid receptor (MR) expression in any of the nuclei examined. Our findings represent a potential mechanism through which antidepressants and glucocorticoids could alter both HPA activity and mood via effects on brainstem, GR, norepinephrine, and serotonin. (C) 2009 Elsevier B.V. All rights reserved.

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