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Am J Physiol Renal Physiol 287: F535-F542, 2004. First published May 4, 2004; doi:10.1152/ajprenal.00394.2003
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Response of descending vasa recta to luminal pressure

Zhong Zhang and Thomas L. Pallone

Department of Medicine, Division of Nephrology, and Department of Physiology, University of Maryland School of Medicine, Baltimore, Maryland 21201-1595

Submitted 6 November 2003 ; accepted in final form 27 April 2004

We tested whether luminal perfusion and pressurization induce an endothelial cytoplasmic Ca2+ ([Ca2+]CYT) response in descending vasa recta (DVR). DVR isolated from the rat outer medulla were cannulated and subjected to free-flow microperfusion (5 nl/min); the onset of which increased [Ca2+]CYT from a baseline of 76 ± 13 to 221 ± 65 nM. A graded increase in luminal pressure from 0 to 45 mmHg in stopped-flow experiments induced a parallel increase in [Ca2+]CYT from a baseline of 74 ± 24 to 194 ± 33 nM at 45 mmHg, with a tendency for [Ca2+]CYT to plateau at pressures >25 mmHg. The removal of extracellular Ca2+ and blockade by either La3+ (10 µM) or SKF-96365 (100 µM) eliminated the response. Luminal pressurization to 25 mmHg increased nitric oxide (NO) generation, a response blocked by NO synthase inhibition or removal of extracellular Ca2+. The NO generation was not affected by the superoxide dismutase mimetic tempol. We conclude that DVR endothelia are mechanosensitive and respond to luminal pressure by elevating [Ca2+]CYT and generating NO. That response might augment medullary perfusion and saliuresis.

medulla; kidney; microcirculation; shear; fura 2; 4,5-diaminofluoroscein



Address for reprint requests and other correspondence: T. L. Pallone, Division of Nephrology, N3W143, Univ. of Maryland at Baltimore, 22 S. Greene St., Baltimore, MD 21201-1595 (E-mail: tpallone{at}medicine.umaryland.edu)




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