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血管紧张素II与肾上腺。

Angiotensin II and the adrenal.

作者信息

Giacchetti G, Opocher G, Sarzani R, Rappelli A, Mantero F

机构信息

Division of Endocrinology, University of Ancona, Italy.

出版信息

Clin Exp Pharmacol Physiol Suppl. 1996;3:S119-24.

PMID:8993850
Abstract
  1. Angiotensin II (AngII) evokes a variety of physiological responses in the adrenal gland. It is the major regulator of aldosterone secretion, in the medulla it enhances catecholamine release and it exerts trophic effects in the adrenal and stimulates growth factor secretion. 2. Angiotensin II acts via binding to specific receptors, located on the plasma membrane. Two pharmacologically distinct AngII receptor subtypes, type 1 (AT1) and type 2 (AT2) receptors, have been identified using the non-peptide antagonists Dup753 and PD 123177, respectively, and cDNA encoding each type have been identified. 3. In the adrenal, the AT1 receptor modulates all the known biological effects of AngII. The expression of the AT1 receptor is modulated at the mRNA and protein levels by many factors: conditions that increase levels of AngII (low sodium diet, renovascular hypertension, AngII infusion) up-regulate AT1 receptor mRNA levels and binding and increase aldosterone secretion. 4. A tissue renin-angiotensin system has been found in the adrenal, suggesting an important paracrine role for AngII in aldosterone regulation. 5. The possible involvement of AT1 receptors in human disease has been investigated by examining the role of AngII receptors in adrenal tumours. Binding and gene expression studies have shown that AngII receptors are abundantly expressed in aldosterone-producing adenoma (APA). 6. Densitometric analysis of AT1 expression in APA showed no significant differences compared with normal and non-tumorous adrenal. In addition, no mutations in the coding sequence of the AT1 receptor have been found to date in adrenal tumours.
摘要
  1. 血管紧张素II(AngII)可引起肾上腺的多种生理反应。它是醛固酮分泌的主要调节因子,在髓质中可增强儿茶酚胺释放,并对肾上腺发挥营养作用,刺激生长因子分泌。2. 血管紧张素II通过与位于质膜上的特异性受体结合发挥作用。使用非肽拮抗剂Dup753和PD 123177分别鉴定出两种药理学上不同的血管紧张素II受体亚型,即1型(AT1)和2型(AT2)受体,并且已经鉴定出编码每种类型的cDNA。3. 在肾上腺中,AT1受体调节血管紧张素II的所有已知生物学效应。AT1受体的表达在mRNA和蛋白质水平受到多种因素的调节:增加血管紧张素II水平的情况(低钠饮食、肾血管性高血压、血管紧张素II输注)可上调AT1受体mRNA水平和结合,并增加醛固酮分泌。4. 在肾上腺中发现了组织肾素-血管紧张素系统,提示血管紧张素II在醛固酮调节中具有重要的旁分泌作用。5. 通过研究血管紧张素II受体在肾上腺肿瘤中的作用,对AT1受体在人类疾病中的可能参与情况进行了研究。结合和基因表达研究表明,血管紧张素II受体在醛固酮瘤(APA)中大量表达。6. 对APA中AT1表达的光密度分析显示,与正常和非肿瘤性肾上腺相比无显著差异。此外,迄今为止在肾上腺肿瘤中未发现AT1受体编码序列的突变。

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