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Research Article Free access | 10.1172/JCI116286

Osmolar regulation of endothelin-1 production by rat inner medullary collecting duct.

D E Kohan and E Padilla

Department of Internal Medicine, Veterans Administration Medical Center, Salt Lake City, Utah 84132.

Find articles by Kohan, D. in: PubMed | Google Scholar

Department of Internal Medicine, Veterans Administration Medical Center, Salt Lake City, Utah 84132.

Find articles by Padilla, E. in: PubMed | Google Scholar

Published March 1, 1993 - More info

Published in Volume 91, Issue 3 on March 1, 1993
J Clin Invest. 1993;91(3):1235–1240. https://doi.org/10.1172/JCI116286.
© 1993 The American Society for Clinical Investigation
Published March 1, 1993 - Version history
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Abstract

Recent evidence has implicated endothelin-1 (ET-1) as an autocrine inhibitor of inner medullary collecting duct (IMCD) sodium and water transport. The regulators of IMCD ET-1 production are, however, largely unknown. Because of the unique hypertonic environment of the IMCD, the effect of varying extracellular tonicity on IMCD ET-1 production was evaluated. Increasing media osmolality from 300 to 450 mosmol with NaCl or mannitol but not urea caused a marked dose- and time-dependent reduction in ET-1 release by and ET-1 mRNA in cultured rat IMCD cells. In contrast, increasing osmolality had no effect on ET-1 production by rat endothelial or mesangial cells. To see if ET-1 varies in a similar manner in vivo, ET-1 production was assessed in volume expanded (lower medullary tonicity) or volume depleted (high medullary tonicity) rats. Urinary ET-1 excretion and inner medulla ET-1 mRNA were significantly reduced in volume depleted as compared to volume expanded animals. These results indicate that extracellular sodium concentration inhibits ET-1 production specifically in IMCD cells. We speculate that extracellular sodium concentration, via regulation of ET-1 production, provides a link between volume status and IMCD sodium and water reabsorption.

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