4.7 Article

Na+-Retaining Action of COX-2 (Cyclooxygenase-2)/EP1 Pathway in the Collecting Duct via Activation of Intrarenal Renin-Angiotensin-Aldosterone System and Epithelial Sodium Channel

期刊

HYPERTENSION
卷 79, 期 6, 页码 1190-1202

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/HYPERTENSIONAHA.121.17245

关键词

collecting duct; cyclooxygenase-2; EP1 receptor; low salt; renin-angiotensin system

资金

  1. National Institutes of Health [HL139689, DK104072, HL135851]
  2. Department of Veterans Affairs [I01 BX004871, IK6BX005223]
  3. American Heart Association [19POST34410068]

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This study found that the CD COX-2/EP1 pathway may play an important role in maintaining Na+ homeostasis during Na+ depletion, at least in part, through activation of the intrarenal renin-angiotensin-aldosterone system and epithelial sodium channel.
Background: The collecting duct (CD) is a major site of both biosynthesis and action of prostaglandin E-2 as highlighted by the predominant expression of COX-2 (cyclooxygenase-2) and some E-prostanoid (EP) subtypes at this nephron site. The purpose of this study was to determine the relevance and mechanism of CD COX-2/prostaglandin E-2/EP1 signaling for the regulation of Na+ hemostasis during Na+ depletion. Methods: Mice with Aqp2Cre-driven deletion of COX-2 (COX-2(fl/fl)Aqp2Cre(+)) or the EP1 subtype (EP(1)(fl/fl)Aqp2Cre(+)) were generated and the Na+-wasting phenotype of these mice during low-salt (LS) intake was examined. EP subtypes responsible for prostaglandin E-2-induced local renin response were analyzed in primary cultured mouse inner medullary CD cells. Results: Following 28-day LS intake, COX-2(fl/fl)Aqp2Cre(+) mice exhibited a higher urinary Na+ excretion and lower cumulative Na+ balance, accompanied with suppressed intrarenal renin, AngII (angiotensin II), and aldosterone, expression of CYP11B2 (cytochrome P450 family 11 subfamily B member 2), and blunted expression of epithelial sodium channel subunits compared to floxed controls (COX-2(fl/fl)Aqp2Cre(-)), whereas no differences were observed for indices of systemic renin-angiotensin-aldosterone system. In cultured CD cells, exposure to prostaglandin E-2 stimulated release of soluble (pro)renin receptor, prorenin/renin and aldosterone and the stimulation was more sensitive to antagonism of EP1 as compared other EP subtypes. Subsequently, EP(1)(fl/fl)Aqp2Cre(+) mice largely recapitulated Na+-wasting phenotype seen in COX-2(fl/fl)Aqp2Cre(+) mice. Conclusions: The study for the first time reports that CD COX-2/EP1 pathway might play a key role in maintenance of Na+ homeostasis in the face of Na+ depletion, at least in part, through activation of intrarenal renin-angiotensin-aldosterone-system and epithelial sodium channel.

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