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The Annals of Thoracic Surgery, Vol 58, 789-794, Copyright © 1994 by The Society of Thoracic Surgeons
R Cartier, F Dagenais, C Hollmann, H Cambron and J Buluran
Chronic exposure to cyclosporine affects vascular reactivity. Experiments
were designed to characterize the endothelium-dependent and
endothelium-independent vascular reactivity of rats exposed to oral
cyclosporin A (CyA). Two subsets of rats (n = 6) were treated with CyA (20
mg/kg/day) and olive oil (cyclosporine vehicle), respectively, for a period
of 8 weeks. Aortic rings (4-5 mm) were suspended for isometric force
measurement in organ chambers containing Krebs Ringer solution (37 degrees
C, 95% O2, 5% CO2). The maximal endothelium-dependent relaxation to
cumulative doses of acetylcholine was significantly decreased in the
CyA-treated aortic rings compared to olive oil-treated ones (data expressed
as percent of initial contraction; CyA, 50% +/- 3% versus olive oil, 37%
+/- 7%; p < 0.05). However, endothelium-dependent relaxations to
histamine and adenosine diphosphate and endothelium- independent relaxation
to sodium nitroprusside were not affected in both groups. An
endothelium-dependent contraction to serotonin and aggregating platelets
were observed in the CyA group, but not in the control group. The
endothelium-independent contraction to norepinephrine was enhanced in the
CyA group (CyA ED50, log -7.66 +/- 0.18 mol/L versus olive oil ED50, log
-7.01 +/- 0.11 mol/L; p < 0.01). These experiments suggest that chronic
exposure to cyclosporine A could contribute to augmenting vascular tone by
(1) decreased release of endothelial relaxing factor mediated by muscarinic
receptors, (2) increased production of endothelium-related constricting
factor mediated by serotoninergic receptors, and (3) greater vascular
smooth muscle sensitivity to circulating catecholamine.
ARTICLES
Chronic exposure to cyclosporine affects endothelial and smooth muscle reactivity in the rat aorta
Department of Cardiovascular Surgery, Montreal Heart Institute, Quebec, Canada.
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