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Am J Physiol Regul Integr Comp Physiol 283: R710-R720, 2002. First published June 6, 2002; doi:10.1152/ajpregu.00522.2001
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Vol. 283, Issue 3, R710-R720, September 2002

Antihypertensive effect of mechanism-based inhibition of renal arachidonic acid omega -hydroxylase activity

Fengyun Xu1, Wesley O. Straub2, Winnie Pak1, Ping Su1, Kristopher G. Maier3, Ming Yu3, Richard J. Roman3, Paul R. Ortiz De Montellano2, and Deanna L. Kroetz1

1 Departments of Biopharmaceutical Sciences and 2 Pharmaceutical Chemistry, School of Pharmacy, University of California, San Francisco, California 94143; and 3 Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin 53226

The cytochrome P-450 eicosanoid 20-hydroxyeicosatetraenoic acid (20-HETE) is a potent vasoconstrictor that is implicated in the regulation of blood pressure. The identification of selective inhibitors of renal 20-HETE formation for use in vivo would facilitate studies to determine the systemic effects of this eicosanoid. We characterized the acetylenic fatty acid sodium 10-undecynyl sulfate (10-SUYS) as a potent and selective mechanism-based inhibitor of renal 20-HETE formation. A single dose of 10-SUYS caused an acute reduction in mean arterial blood pressure in 8-wk-old spontaneously hypertensive rats. The decrease in mean arterial pressure was maximal 6 h after 10-SUYS treatment (17.9 ± 3.2 mmHg; P < 0.05), and blood pressure returned to baseline levels within 24 h after treatment. Treatment with 10-SUYS was associated with a decrease in urinary 20-HETE formation in vivo and attenuation of the vasoconstrictor response of renal interlobar arteries to ANG II in vitro. These results provide further evidence that 20-HETE plays an important role in the regulation of blood pressure in the spontaneously hypertensive rat.

spontaneously hypertensive rat; cytochrome P-450; sodium 10-undecynyl sulfate; 20-hydroxyeicosatetraenoic acid


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