Renal Effects of Prostaglandins and Cyclooxygenase-2 Inhibitors.
- Author:
Gheun Ho KIM
1
Author Information
- Publication Type:Review
- Keywords: prostaglandins; kidney; sodium; kidney concentrating ability
- MeSH: Aldosterone; Aquaporin 2; Bartter Syndrome; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxygenase Inhibitors; Diabetes Insipidus, Nephrogenic; Dinoprostone; Epoprostenol; Extremities; Glomerular Filtration Rate; Kidney; Kidney Concentrating Ability; Loop of Henle; Perfusion; Potassium; Prostaglandins; Renal Circulation; Renin; Renin-Angiotensin System; Sodium; Water
- From:Electrolytes & Blood Pressure 2008;6(1):35-41
- CountryRepublic of Korea
- Language:English
- Abstract: Prostaglandins (PGs) with best-defined renal functions are PGE2 and prostacyclin (PGI2). These vasodilatory PGs increase renal blood flow and glomerular filtration rate under conditions associated with decreased actual or effective circulating volume, resulting in greater tubular flow and secretion of potassium. Under conditions of decreased renal perfusion, the production of renal PGs serves as an important compensatory mechanism. PGI2 (and possibly PGE2) increases potassium secretion mainly by stimulating secretion of renin and activating the renin-angiotensin system, which leads to increased secretion of aldosterone. In addition, PGE2 is involved in the regulation of sodium and water reabsorption and acts as a counterregulatory factor under conditions of increased sodium reabsorption. PGE2 decreases sodium reabsorption at the thick ascending limb of the loop of Henle probably via inhibition of the Na+-K+-2Cl-cotransporter type 2 (NKCC2). Cyclooxygenase inhibitors may enhance urinary concentrating ability in part through effects to upregulate NKCC2 in the thick ascending limb of Henle's loop and aquaporin-2 in the collecting duct. Thus, they may be useful to treat Bartter's syndrome and nephrogenic diabetes insipidus.
