One-hour exposure to University of Wisconsin solution does not impair endothelium-dependent relaxation or damage vascular smooth muscle of epicardial coronary arteries

S. T. Ekin, P. J. Pearson, P. R B Evora, Hartzell V Schaff

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

To determine whether University of Wisconsin solution impairs production of endothelium-derived relaxing factor or damages vascular smooth muscle function of epicardial coronary arteries, isolated segments of canine left circumflex coronary artery were exposed to either cold (7° C) or normothermic (37° C) University of Wisconsin solution or to cold (30° C) or normothermic (37° C) physiologic salt solution in vitro for 60 minutes. After incubation with the solutions, the vascular segments were studied in vitro in organ chambers. Exposure to cold or to normothermic University of Wisconsin solution did not alter endothelium-dependent relaxation (either maximal relaxation or ED50) of the segments in response to adenosine diphosphate or acetylcholine (10-9 to 10-4 mol/L). Also, contraction of the segments in response to potassium ions (voltage-dependent) or prostaglandin F(2α) (receptor-dependent) and relaxation in response to isoproterenol (cyclic AMP-mediated) or sodium nitroprusside (cyclic GMP- mediated) were unaltered after exposure to cold University of Wisconsin solution. Direct exposure to normothermic University of Wisconsin solution induced transient vasoconstriction in segments with or without endothelium. Thus University of Wisconsin solution does not irreversibly impair release of endothelium-derived relaxing factor or alter function of vascular smooth muscle in epicardial coronary arteries.

Original languageEnglish (US)
Pages (from-to)624-633
Number of pages10
JournalJournal of Heart and Lung Transplantation
Volume12
Issue number4
StatePublished - 1993

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Vascular Smooth Muscle
Endothelium
Coronary Vessels
Endothelium-Dependent Relaxing Factors
Cyclic GMP
Prostaglandins F
Nitroprusside
Vasoconstriction
Isoproterenol
Cyclic AMP
Adenosine Diphosphate
Acetylcholine
Blood Vessels
Canidae
Potassium
Salts
Ions

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Surgery
  • Transplantation

Cite this

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title = "One-hour exposure to University of Wisconsin solution does not impair endothelium-dependent relaxation or damage vascular smooth muscle of epicardial coronary arteries",
abstract = "To determine whether University of Wisconsin solution impairs production of endothelium-derived relaxing factor or damages vascular smooth muscle function of epicardial coronary arteries, isolated segments of canine left circumflex coronary artery were exposed to either cold (7° C) or normothermic (37° C) University of Wisconsin solution or to cold (30° C) or normothermic (37° C) physiologic salt solution in vitro for 60 minutes. After incubation with the solutions, the vascular segments were studied in vitro in organ chambers. Exposure to cold or to normothermic University of Wisconsin solution did not alter endothelium-dependent relaxation (either maximal relaxation or ED50) of the segments in response to adenosine diphosphate or acetylcholine (10-9 to 10-4 mol/L). Also, contraction of the segments in response to potassium ions (voltage-dependent) or prostaglandin F(2α) (receptor-dependent) and relaxation in response to isoproterenol (cyclic AMP-mediated) or sodium nitroprusside (cyclic GMP- mediated) were unaltered after exposure to cold University of Wisconsin solution. Direct exposure to normothermic University of Wisconsin solution induced transient vasoconstriction in segments with or without endothelium. Thus University of Wisconsin solution does not irreversibly impair release of endothelium-derived relaxing factor or alter function of vascular smooth muscle in epicardial coronary arteries.",
author = "Ekin, {S. T.} and Pearson, {P. J.} and Evora, {P. R B} and Schaff, {Hartzell V}",
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AU - Ekin, S. T.

AU - Pearson, P. J.

AU - Evora, P. R B

AU - Schaff, Hartzell V

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