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MK-801诱导大鼠下丘脑小细胞室旁核中c-fos和CRF mRNA的表达。

Induction of c-fos and CRF mRNA by MK-801 in the parvocellular paraventricular nucleus of the rat hypothalamus.

作者信息

Lee S, Rivier C, Torres G

机构信息

Clayton Foundation Laboratory for Peptide Biology, Salk Institute, La Jolla, CA 92031.

出版信息

Brain Res Mol Brain Res. 1994 Jul;24(1-4):192-8. doi: 10.1016/0169-328x(94)90132-5.

Abstract

The non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist dizocilpine maleate (MK-801) stimulates the secretion of adrenocorticotropin hormone (ACTH). As corticotropin-releasing factor (CRF) represents the primary modulator of this secretion, we tested the hypothesis that the ability of MK-801 to activate the hypothalamic-pituitary-adrenal (HPA) axis was modulated through actions at the hypothalamic level that modulate the secretion of CRF. Induction of the immediate-early gene c-fos, as well as of CRF mRNA within the paraventricular nucleus (PVN) of the rat hypothalamus, was examined following the intraperitoneally administration of MK-801 (1 mg/kg). MK-801 markedly increased the expression of Fos-like protein in parvocellular nerve cells of the PVN within 60 min of systemic treatment, and double labeling immunocytochemistry indicated that Fos was primarily localized in CRF-containing neurons of the PVN. MK-801 also significantly increased CRF biosynthesis as detected by in situ hybridization, thus suggesting that c-fos could be involved in the regulation of CRF genes. Taken together, these results suggest that MK-801 stimulates the rat HPA axis probably through the neuronal gene expression of PVN CRF. The significance of these data is discussed in terms of hypothalamic NMDA receptor blockade and subsequent transcriptional regulation of CRF by immediate-early genes.

摘要

非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂马来酸氯胺酮(MK-801)可刺激促肾上腺皮质激素(ACTH)的分泌。由于促肾上腺皮质激素释放因子(CRF)是这种分泌的主要调节因子,我们检验了以下假设:MK-801激活下丘脑-垂体-肾上腺(HPA)轴的能力是通过在下丘脑水平调节CRF分泌的作用来调节的。在腹腔注射MK-801(1mg/kg)后,检测大鼠下丘脑室旁核(PVN)内即刻早期基因c-fos以及CRF mRNA的诱导情况。全身给药后60分钟内,MK-801显著增加了PVN小细胞神经细胞中Fos样蛋白的表达,双重标记免疫细胞化学表明Fos主要定位于PVN中含CRF的神经元。原位杂交检测显示,MK-801也显著增加了CRF的生物合成,因此提示c-fos可能参与CRF基因的调控。综上所述,这些结果表明MK-801可能通过PVN中CRF的神经元基因表达来刺激大鼠HPA轴。本文根据下丘脑NMDA受体阻断以及即刻早期基因对CRF的后续转录调控对这些数据的意义进行了讨论。

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