Long term Rho-kinase inhibition ameliorates endothelial dysfunction in LDL-Receptor deficient mice |
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Authors: | Steioff Kerstin Rütten Hartmut Busch Andreas E Plettenburg Oliver Ivashchenko Yuri Löhn Matthias |
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Affiliation: | Sanofi-Aventis Pharma GmbH, Therapeutic Department Cardiovascular Diseases, Industriepark H?chst, 65926 Frankfurt am Main, Germany. |
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Abstract: | Chronic inhibition of Rho-kinase has been recently implicated in retardation of atherogenesis induced by high-fat diet in low-density lipoprotein receptor deficient (LDLR-/-) mice. However, it remains to be examined whether long-term Rho-kinase inhibition will reduce vascular dysfunction in this model. LDLR-/- mice on a high-fat diet were treated either with saline (LDLR-/-) or with the Rho-kinase inhibitor Fasudil (HA1077, 5-Isoquinolinesulfonyl homopiperazine, 100 mg/kg/day by gavage, LDLR-/- +Fasudil) for 10 weeks. Fasudil-treatment normalized endothelial function (measured by means of endothelium-dependent vasorelaxation) in LDLR-/- +Fasudil, to the level of controls (C57BL/6J). No tolerance toward Rho-kinase inhibition has been detected in Fasudil-treated animals. We conclude that long-term Rho-kinase inhibition normalizes endothelial function without development of tolerance. |
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