Endothelial Nitric Oxide Synthase in Mice Mevastatin, an HMG-CoA Reductase Inhibitor, Reduces Stroke Damage and Upregulates

نویسندگان

  • Michael A. Moskowitz
  • Sepideh Amin-Hanjani
  • Nancy E. Stagliano
  • Masaru Yamada
  • Paul L. Huang
  • James K. Liao
چکیده

Sepideh Amin-Hanjani, Nancy E. Stagliano, Masaru Yamada, Paul L. Huang, James K. Liao Endothelial Nitric Oxide Synthase in Mice Mevastatin, an HMG-CoA Reductase Inhibitor, Reduces Stroke Damage and Upregulates Print ISSN: 0039-2499. Online ISSN: 1524-4628 Copyright © 2001 American Heart Association, Inc. All rights reserved. is published by the American Heart Association, 7272 Greenville Avenue, Dallas, TX 75231 Stroke doi: 10.1161/01.STR.32.4.98

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Mevastatin, an HMG-CoA reductase inhibitor, reduces stroke damage and upregulates endothelial nitric oxide synthase in mice.

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Upregulation of endothelial nitric oxide synthase by HMG CoA reductase inhibitors.

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Direct vascular and cardioprotective effects of rosuvastatin, a new HMG-CoA reductase inhibitor.

OBJECTIVE We examined the possible effects of a novel 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor, rosuvastatin, on endothelial nitric oxide (NO) production and myocardial ischemia-reperfusion injury. BACKGROUND Recent studies suggest that HMG-CoA reductase inhibitors promote vascular endothelial function through enhanced endothelial NO production. However, it is uncle...

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Statins induce angiogenesis, neurogenesis, and synaptogenesis after stroke.

We demonstrate that the 3-hydroxy-3-methyl-glutaryl-coenzyme A (HMG-CoA) reductase inhibitors atorvastatin and simvastatin enhance functional outcome and induce brain plasticity when administered after stroke to rats. With atorvastatin treatment initiated 1 day after stroke, animals exhibited significant increases in vascular endothelial growth factor, cyclic guanosine monophosphate, angiogenes...

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تاریخ انتشار 2001