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Hypertension. 1998;31:1305-1310

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(Hypertension. 1998;31:1305-1310.)
© 1998 American Heart Association, Inc.


Scientific Contributions

Losartan but Not Verapamil Inhibits Angiotensin II–Induced Tissue Endothelin-1 Increase

Role of Blood Pressure and Endothelial Function

Livius V. d'Uscio; Sidney Shaw; Matthias Barton; ; Thomas F. Lüscher

From Cardiovascular Research, Institute of Physiology, University of Zürich, and the Division of Cardiology, University Hospital, Zürich, and the Division of Cardiology and Department of Clinical Research, University Hospital, Bern (S.S.), Switzerland.

Correspondence to Thomas F. Lüscher, MD, FACC, FESC, Professor and Head of Cardiology, University Hospital, CH-8091 Zürich, Switzerland. E-mail 100771.1237{at}compuserve.com

Abstract—Endothelin partially mediates angiotensin (Ang) II–induced vascular changes in vivo. This study investigated the effects of the angiotensin type 1 receptor antagonist losartan and the calcium channel blocker verapamil on vascular reactivity and tissue endothelin-1 levels in aortas of Wistar-Kyoto rats treated for 2 weeks with Ang II (200 ng · kg-1 · min-1). Ang II increased systolic blood pressure (39±4 mm Hg, P<0.05). Concomitant treatment with losartan abolished the Ang II–induced pressure increase (P<0.05), whereas verapamil reduced it only partially (P<0.05). In the aortas of rats with Ang II–induced hypertension, tissue endothelin-1 content was increased threefold and contractions to endothelin-1 were impaired (P<0.05). Interestingly, these alterations were normalized by losartan (P<0.05) but not by verapamil. Hence, there was a strong, negative correlation between contractions to endothelin-1 and tissue endothelin-1 content (r=-0.733, P<0.0001). In contrast, both antihypertensive drugs normalized impaired endothelium-dependent relaxations to acetylcholine and reduced the sensitivity of vascular smooth muscle to sodium nitroprusside compared with Ang II–treated rats (P<0.05). Ang II–induced hypertension enhanced endothelium-dependent contractions to acetylcholine, and these were normalized by either drug. In conclusion, these findings suggest that long-term treatment with Ang II modulates endothelin-1 protein expression in the rat aorta. Although both antihypertensive agents lowered blood pressure and normalized endothelial function, only losartan prevented the increase in tissue endothelin-1 content, suggesting that angiotensin type 1 receptor antagonists but not calcium antagonists modulate tissue endothelin-1 in vivo.


Key Words: angiotensin II • endothelin • endothelium • losartan • verapamil • aorta




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