Literature DB >> 12364322

Reduction of blood pressure, plasma cholesterol, and atherosclerosis by elevated endothelial nitric oxide.

Rien van Haperen1, Monique de Waard, Elza van Deel, Barend Mees, Michael Kutryk, Thijs van Aken, Jaap Hamming, Frank Grosveld, Dirk J Duncker, Rini de Crom.   

Abstract

In the vascular system, nitric oxide is generated by endothelial NO synthase (eNOS). NO has pleiotropic effects, most of which are believed to be atheroprotective. Therefore, it has been argued that patients suffering from cardiovascular disease could benefit from an increase in eNOS activity. However, increased NO production can cause oxidative damage, cell toxicity, and apoptosis and hence could be atherogenic rather than beneficial. To study the in vivo effects of increased eNOS activity, we created transgenic mice overexpressing human eNOS. Aortic blood pressure was approximately 20 mm Hg lower in the transgenic mice compared with control mice because of lower systemic vascular resistance. The effects of eNOS overexpression on diet-induced atherosclerosis were studied in apolipoprotein E-deficient mice. Elevation of eNOS activity decreased blood pressure ( approximately 20 mm Hg) and plasma levels of cholesterol ( approximately 17%), resulting in a reduction in atherosclerotic lesions by 40%. We conclude that an increase in eNOS activity is beneficial and provides protection against atherosclerosis.

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Year:  2002        PMID: 12364322     DOI: 10.1074/jbc.M209477200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  28 in total

1.  FoxOs integrate pleiotropic actions of insulin in vascular endothelium to protect mice from atherosclerosis.

Authors:  Kyoichiro Tsuchiya; Jun Tanaka; Yu Shuiqing; Carrie L Welch; Ronald A DePinho; Ira Tabas; Alan R Tall; Ira J Goldberg; Domenico Accili
Journal:  Cell Metab       Date:  2012-03-07       Impact factor: 27.287

Review 2.  Nitric oxide synthases in the pathogenesis of cardiovascular disease: lessons from genetically modified mice.

Authors:  Hiroaki Shimokawa; Masato Tsutsui
Journal:  Pflugers Arch       Date:  2010-02-24       Impact factor: 3.657

Review 3.  Endothelial arginase: a new target in atherosclerosis.

Authors:  Zhihong Yang; Xiu-Fen Ming
Journal:  Curr Hypertens Rep       Date:  2006-04       Impact factor: 5.369

4.  An activated renin-angiotensin system maintains normal blood pressure in aryl hydrocarbon receptor heterozygous mice but not in null mice.

Authors:  Nan Zhang; Larry N Agbor; Jason A Scott; Tyler Zalobowski; Khalid M Elased; Alicia Trujillo; Melissa Skelton Duke; Valerie Wolf; Mary T Walsh; Jerry L Born; Linda A Felton; Jian Wang; Wei Wang; Nancy L Kanagy; Mary K Walker
Journal:  Biochem Pharmacol       Date:  2010-03-30       Impact factor: 5.858

5.  Endothelial cell-specific aryl hydrocarbon receptor knockout mice exhibit hypotension mediated, in part, by an attenuated angiotensin II responsiveness.

Authors:  Larry N Agbor; Khalid M Elased; Mary K Walker
Journal:  Biochem Pharmacol       Date:  2011-06-13       Impact factor: 5.858

6.  Pathophysiology of hypertension in the absence of nitric oxide/cyclic GMP signaling.

Authors:  Robrecht Thoonen; Patrick Y Sips; Kenneth D Bloch; Emmanuel S Buys
Journal:  Curr Hypertens Rep       Date:  2013-02       Impact factor: 5.369

7.  Functional expression of endothelial nitric oxide synthase fused to green fluorescent protein in transgenic mice.

Authors:  Rien van Haperen; Caroline Cheng; Barend M E Mees; Elza van Deel; Monique de Waard; Luc C A van Damme; Teus van Gent; Thijs van Aken; Rob Krams; Dirk J Duncker; Rini de Crom
Journal:  Am J Pathol       Date:  2003-10       Impact factor: 4.307

8.  Endothelial function in aorta segments of apolipoprotein E-deficient mice before development of atherosclerotic lesions.

Authors:  Paul Fransen; Tim Van Assche; Pieter-Jan Guns; Cor E Van Hove; Gilles W De Keulenaer; Arnold G Herman; Hidde Bult
Journal:  Pflugers Arch       Date:  2007-09-27       Impact factor: 3.657

9.  Endothelial nitric oxide synthase inhibits G12/13 and rho-kinase activated by the angiotensin II type-1 receptor: implication in vascular migration.

Authors:  Hiroyuki Suzuki; Keita Kimura; Heigoro Shirai; Kunie Eguchi; Sadaharu Higuchi; Akinari Hinoki; Kazuhiro Ishimaru; Eugen Brailoiu; Danny N Dhanasekaran; Laura N Stemmle; Timothy A Fields; Gerald D Frank; Michael V Autieri; Satoru Eguchi
Journal:  Arterioscler Thromb Vasc Biol       Date:  2008-12-18       Impact factor: 8.311

10.  Chronic ethanol ingestion increases aortic endothelial nitric oxide synthase expression and nitric oxide production in the rat.

Authors:  Dean J Kleinhenz; Roy L Sutliff; John A Polikandriotis; Erik R Walp; Sergey I Dikalov; David M Guidot; C Michael Hart
Journal:  Alcohol Clin Exp Res       Date:  2007-11-20       Impact factor: 3.455

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