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J Am Soc Nephrol 15:558-565, 2004
© 2004 American Society of Nephrology


BASIC SCIENCE

Aldosterone Decreases UT-A1 Urea Transporter Expression via the Mineralocorticoid Receptor

Randy A. Gertner*, Janet D. Klein*, James L. Bailey*, Dong-un Kim*, Xiao H. Luo*, Serena M. Bagnasco{dagger} and Jeff M. Sands*,{ddagger}

*Renal Division, Department of Medicine, {dagger}Department of Pathology, and {ddagger}Department of Physiology, Emory University School of Medicine, Atlanta, Georgia

Correspondence to Dr. Randy A. Gertner, Emory University School of Medicine, Renal Division, WMRB Room 338, 1639 Pierce Drive, NE, Atlanta, GA 30322. Phone: 404-727-2525; FAX: 404-727-3425; E-mail: rag145{at}hotmail.com

ABSTRACT. Adrenalectomy in rats is associated with urinary concentrating and diluting defects. This study tested the effect of adrenal steroids on the UT-A1 urea transporter because it is involved in the urine-concentrating mechanism. Rats were adrenalectomized and given normal saline for 14 d, after which they received (1) vehicle, (2) aldosterone, or (3) spironolactone plus aldosterone. Adrenalectomy alone significantly increased UT-A1 protein in the inner medullary tip after 7 d, whereas aldosterone repletion reversed the effect. Spironolactone blocked the aldosterone-induced decrease in UT-A1, indicating that aldosterone was working via the mineralocorticoid receptor. For verifying that glucocorticoids downregulate UT-A1 protein through a different receptor, three groups of adrenalectomized rats were prepared: (1) vehicle, (2) adrenalectomy plus dexamethasone, and (3) adrenalectomy plus dexamethasone and spironolactone. Dexamethasone significantly reversed UT-A1 protein abundance increase in the inner medullary tip of adrenalectomized rats. When spironolactone was given with dexamethasone, it did not affect the dexamethasone-induced decrease in UT-A1. There was no significant change in serum vasopressin level, aquaporin 2, or Na+-K+-2Cl- co-transporter NKCC2/BSC1 protein abundances or UT-A1 mRNA abundance in any of the groups. In conclusion, either mineralocorticoids or glucocorticoids can downregulate UT-A1 protein. The decrease in UT-A1 does not require both steroid hormones, and each works through a different receptor.




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