Expression of the epithelial Na⁺ channel and other components of an aldosterone response pathway in human adrenocortical cells

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• 作者：Timothy J. Burton ; Georgina Cope ; Jing Wang ; Joalice C. Sim ; Elena A.B. Azizan ; Kevin M. O'Shaughnessy ; Morris J. Brown
• 关键词：Epithelial Na⁺ channel ; Aldosterone ; Adrenal cortex
• 刊名：European Journal of Pharmacology
• 出版年：2009
• 出版时间：24 June 2009
• 年：2009
• 卷：613
• 期：1-3
• 页码：176-181
• 全文大小：368 K

文摘

We have unexpectedly found expression of the epithelial Na⁺ channel (ENaC) in human adrenocortical cells and tested the hypothesis that these cells contain the components of an aldosterone response pathway. Tissue was obtained from patients undergoing adrenalectomy and mRNA and protein expression of recognised components of an aldosterone-response pathway were determined by RT-PCR and Western blotting. The effects of mineralocorticoid receptor agonists and antagonists, amiloride analogues, and extracellular Na⁺ on basal and stimulated aldosterone release from immortalised (H295R) cells were determined by radioimmunoassay. Expression of mRNA for α-, β- and γ-subunits of ENaC, the mineralocorticoid receptor, Nedd4L, Sgk1 and 11β hydroxysteroid dehydrogenase type II was confirmed in human adrenal cortex. Using Western blotting α-, β- and γ-ENaC expression was demonstrated in adrenocortical cells. Measurements of 24 h aldosterone release from H295R cells showed stimulation by K⁺ and angiotensin II, suppression by both Na⁺ and high-concentration 5-(N-ethyl-N-isopropyl) amiloride (EIPA, blocker of Na⁺–H⁺ exchange) and no change with benzamil (ENaC blocker). ²²Na-uptake into H295R cells was inhibited by EIPA, but not by benzamil. Our experiments suggest that the components of an aldosterone response pathway are present in human adrenal cortex. Studies in H295R cells, however, suggest that ENaC is not an important mediator of ²²Na-uptake or aldosterone production. Further studies are required to determine the importance of an adrenal aldosterone response pathway.