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Article has an altmetric score of 3

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Research Article Free access | 10.1172/JCI119426

Vascular estrogen receptors and endothelium-derived nitric oxide production in the mouse aorta. Gender difference and effect of estrogen receptor gene disruption.

G M Rubanyi, A D Freay, K Kauser, D Sukovich, G Burton, D B Lubahn, J F Couse, S W Curtis, and K S Korach

Department of Cardiovascular Research, Berlex Biosciences, Richmond, California 94804-0099, USA. gabor_rubanyi@berlex.com

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Department of Cardiovascular Research, Berlex Biosciences, Richmond, California 94804-0099, USA. gabor_rubanyi@berlex.com

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Department of Cardiovascular Research, Berlex Biosciences, Richmond, California 94804-0099, USA. gabor_rubanyi@berlex.com

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Department of Cardiovascular Research, Berlex Biosciences, Richmond, California 94804-0099, USA. gabor_rubanyi@berlex.com

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Department of Cardiovascular Research, Berlex Biosciences, Richmond, California 94804-0099, USA. gabor_rubanyi@berlex.com

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Department of Cardiovascular Research, Berlex Biosciences, Richmond, California 94804-0099, USA. gabor_rubanyi@berlex.com

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

Department of Cardiovascular Research, Berlex Biosciences, Richmond, California 94804-0099, USA. gabor_rubanyi@berlex.com

Find articles by Couse, J. in: PubMed | Google Scholar

Department of Cardiovascular Research, Berlex Biosciences, Richmond, California 94804-0099, USA. gabor_rubanyi@berlex.com

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Department of Cardiovascular Research, Berlex Biosciences, Richmond, California 94804-0099, USA. gabor_rubanyi@berlex.com

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Published May 15, 1997 - More info

Published in Volume 99, Issue 10 on May 15, 1997
J Clin Invest. 1997;99(10):2429–2437. https://doi.org/10.1172/JCI119426.
© 1997 The American Society for Clinical Investigation
Published May 15, 1997 - Version history
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Abstract

The present study was designed to test the hypothesis that estrogen receptors (ER) in the blood vessel wall play a role in the modulation of the release of endothelium-derived nitric oxide (EDNO). Both basal and stimulated release of EDNO were determined in aortic rings isolated from female and male wild-type and male homozygous estrogen receptor knock-out (ERKO) mice. 125I-17beta-estradiol binding in aortic tissue showed significantly more high affinity cytosolic- nuclear-binding sites in male compared with female wildtype mice. Estrogen receptor transcripts were present in the aorta of male wild-type mice, but they were absent in male ERKO animals. Basal release of EDNO (determined by endothelium-dependent contraction caused by NG-nitro-arginine) was significantly higher in aorta of wild-type male mice compared with wild-type female mice, and significantly lower in the aorta of male ERKO compared with male wild-type mice. Acetylcholine-induced endothelium-dependent relaxation was similar in all groups studied. No difference was observed in the activity of calcium-dependent nitric oxide synthase in homogenates of lungs and brain taken from male wild-type and ERKO mice. These studies show a significant association between the number of estrogen receptors and basal release of EDNO in the aorta of mice, and suggest that decreased vascular estrogen receptor number may represent a novel risk factor for cardiovascular diseases.

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