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皮质类固醇激素对海马5-羟色胺1a受体的转录调控。

Transcriptional regulation of hippocampal 5-HT1a receptors by corticosteroid hormones.

作者信息

Zhong P, Ciaranello R D

机构信息

Nancy Pritzker Laboratory of Developmental and Molecular Neurobiology, Stanford University Medical Center, CA 94305-5485, USA.

出版信息

Brain Res Mol Brain Res. 1995 Mar;29(1):23-34. doi: 10.1016/0169-328x(94)00225-4.

DOI:10.1016/0169-328x(94)00225-4
PMID:7769998
Abstract

5-HT1a receptors in the hippocampus play a critical role in modulating limbic system output. The activity and level of 5-HT1a receptors are modulated by glucocorticoid levels. The present study was undertaken to test the hypothesis that glucocorticoids attenuate the transcriptional activity of the 5-HT1a receptor gene. Using in situ hybridization and RNase protection assays, we observed a substantial increase in 5-HT1a mRNA expression after adrenalectomy in the same hippocampal regions in which 5-HT1a binding sites are increased. This increase in 5-HT1a mRNA expression occurs as early as 1 h after adrenalectomy and precedes the increase in receptor binding sites. Further in situ hybridization analysis showed that 5-HT1a mRNA is increased within individual hippocampal cells after adrenalectomy. Administration of dexamethasone completely prevents the adrenalectomy-induced elevation in hippocampal 5-HT1a receptor mRNA. Nuclear run-on assays showed that the rate of transcription of 5-HT1a mRNA after adrenalectomy increased 70% above the rate from control preparations and could be reduced to basal levels by the administration of dexamethasone. Adrenalectomy did not cause an increase in functional coupling of 5-HT1a receptors to adenylyl cyclase or phospholipase C. These results suggest that transcription of hippocampal 5-HT1a receptor mRNA is under negative regulation by corticosteroid hormones.

摘要

海马体中的5-羟色胺1a(5-HT1a)受体在调节边缘系统输出方面发挥着关键作用。5-HT1a受体的活性和水平受糖皮质激素水平的调节。本研究旨在验证糖皮质激素会减弱5-HT1a受体基因转录活性这一假设。通过原位杂交和核糖核酸酶保护分析,我们观察到,在5-HT1a结合位点增加的相同海马区,肾上腺切除术后5-HT1a信使核糖核酸(mRNA)表达大幅增加。这种5-HT1a mRNA表达的增加早在肾上腺切除术后1小时就出现了,且先于受体结合位点的增加。进一步的原位杂交分析表明,肾上腺切除术后单个海马细胞内的5-HT1a mRNA增加。地塞米松给药完全阻止了肾上腺切除诱导的海马5-HT1a受体mRNA升高。核转录分析表明,肾上腺切除术后5-HT1a mRNA的转录速率比对照制剂的转录速率高出70%,并且通过地塞米松给药可降至基础水平。肾上腺切除并未导致5-HT1a受体与腺苷酸环化酶或磷脂酶C的功能偶联增加。这些结果表明,海马5-HT1a受体mRNA的转录受皮质类固醇激素的负调控。

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