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Cardioprotective effect of hydroxyfasudil as a specific Rho-kinase inhibitor, on ischemia-reperfusion injury in canine coronary microvessels in vivo.

Abstract
Rho-kinase modulates calcium sensitivity of the myosin light chain in smooth muscle cells and has been implicated as playing a pathogenetic role in cardiovascular disorders. This paper was aimed to determine whether hydroxyfasudil (a specific Rho-kinase inhibitor) exerts cardioprotective effect on coronary ischemia-reperfusion (I/R) injury, and if so, whether NO is involved. Canine subepicardial small arteries (diameter > or = 100 microm) and arterioles (diameter < 100 microm) were observed by a CCD intravital microscope during coronary I/R. Coronary vascular responses to endothelium-dependent (acetylcholine) and -independent (papaverine) vasodilators were examined after I/R under three conditions: control, preconditioning, and hydroxyfasudil. Coronary I/R significantly impaired coronary vasodilation to acetylcholine, whereas hydroxyfasudil completely preserved the responses, as did preconditioning. Hydroxyfasudil also significantly reduced myocardial infarct size. These results indicated that hydroxyfasudil exerts cardioprotective effects on coronary I/R injury in vivo, for which NO-mediated mechanism may be involved.
AuthorsToyotaka Yada, Hiroaki Shimokawa, Fumihiko Kajiya
JournalClinical hemorheology and microcirculation (Clin Hemorheol Microcirc) Vol. 34 Issue 1-2 Pg. 177-83 ( 2006) ISSN: 1386-0291 [Print] Netherlands
PMID16543634 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Cardiotonic Agents
  • Enzyme Inhibitors
  • hydroxyfasudil
  • Nitric Oxide
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • rho GTP-Binding Proteins
Topics
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine (analogs & derivatives, pharmacology)
  • Animals
  • Cardiotonic Agents (pharmacology)
  • Coronary Circulation (drug effects)
  • Dogs
  • Enzyme Inhibitors
  • Ischemic Preconditioning, Myocardial
  • Microcirculation (pathology)
  • Myocardial Reperfusion Injury (drug therapy)
  • Nitric Oxide (physiology)
  • rho GTP-Binding Proteins (antagonists & inhibitors)

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