Suppr超能文献

促肾上腺皮质激素释放因子(CRF)和尿皮质素以CRF受体类型特异性方式,对人和大鼠肾上腺中的儿茶酚胺分泌进行差异调节。

Corticotropin-releasing factor (CRF) and the urocortins differentially regulate catecholamine secretion in human and rat adrenals, in a CRF receptor type-specific manner.

作者信息

Dermitzaki E, Tsatsanis C, Minas V, Chatzaki E, Charalampopoulos I, Venihaki M, Androulidaki A, Lambropoulou M, Spiess J, Michalodimitrakis E, Gravanis A, Margioris A N

机构信息

Department of Clinical Chemistry-Biochemistry, School of Medicine, University of Crete, Heraklion GR-710 03, Crete, Greece.

出版信息

Endocrinology. 2007 Apr;148(4):1524-38. doi: 10.1210/en.2006-0967. Epub 2006 Dec 28.

Abstract

Corticotropin-releasing factor (CRF) affects catecholamine production both centrally and peripherally. The aim of the present work was to examine the presence of CRF, its related peptides, and their receptors in the medulla of human and rat adrenals and their direct effect on catecholamine synthesis and secretion. CRF, urocortin I (UCN1), urocortin II (UCN2), and CRF receptor type 1 (CRF1) and 2 (CRF2) were present in human and rat adrenal medulla as well as the PC12 pheochromocytoma cells by immunocytochemistry, immunofluorescence, and RT-PCR. Exposure of dispersed human and rat adrenal chromaffin cells to CRF1 receptor agonists induced catecholamine secretion in a dose-dependent manner, an effect peaking at 30 min, whereas CRF2 receptor agonists suppressed catecholamine secretion. The respective effects were blocked by CRF1 and CRF2 antagonists. CRF peptides affected catecholamine secretion via changes of subplasmaliminal actin filament polymerization. CRF peptides also affected catecholamine synthesis. In rat chromaffin and PC12 cells, CRF1 and CRF2 agonists induced catecholamine synthesis via tyrosine hydroxylase. However, in human chromaffin cells, activation of CRF1 receptors induced tyrosine hydroxylase, whereas activation of CRF2 suppressed it. In conclusion, it appears that a complex intraadrenal CRF-UCN/CRF-receptor system exists in both human and rat adrenals controlling catecholamine secretion and synthesis.

摘要

促肾上腺皮质激素释放因子(CRF)在中枢和外周均影响儿茶酚胺的产生。本研究的目的是检测人及大鼠肾上腺髓质中CRF及其相关肽类和它们的受体的存在情况,以及它们对儿茶酚胺合成和分泌的直接影响。通过免疫细胞化学、免疫荧光和逆转录聚合酶链反应(RT-PCR)检测发现,人及大鼠肾上腺髓质以及嗜铬细胞瘤PC12细胞中存在CRF、尿皮质素I(UCN1)、尿皮质素II(UCN2)以及1型CRF受体(CRF1)和2型CRF受体(CRF2)。将分离的人及大鼠肾上腺嗜铬细胞暴露于CRF1受体激动剂下,可诱导儿茶酚胺分泌呈剂量依赖性,此效应在30分钟时达到峰值,而CRF2受体激动剂则抑制儿茶酚胺分泌。相应的效应可被CRF1和CRF2拮抗剂阻断。CRF肽类通过改变质膜下肌动蛋白丝聚合来影响儿茶酚胺分泌。CRF肽类也影响儿茶酚胺合成。在大鼠嗜铬细胞和PC12细胞中,CRF1和CRF2激动剂通过酪氨酸羟化酶诱导儿茶酚胺合成。然而,在人嗜铬细胞中,CRF1受体激活可诱导酪氨酸羟化酶,而CRF2受体激活则抑制它。总之,人及大鼠肾上腺中似乎存在一个复杂的肾上腺内CRF-UCN/CRF受体系统,该系统控制着儿茶酚胺的分泌和合成。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验