Indigo carmine enhances phenylephrine-induced contractions in an isolated rat aorta

BackgroundThe intravenous administration of indigo carmine has been reported to produce transiently increased blood pressure in patients. The goal of this in vitro study was to examine the effect of indigo carmine on phenylephrine-induced contractions in an isolated rat aorta and to determine the as...

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Main Authors: Yun Suk Choi, Seong-Ho Ok, Seung Min Lee, Sang-Seung Park, Yu Mi Ha, Ki Churl Chang, Hye Jung Kim, Il-Woo Shin, Ju-Tae Sohn
Format: Article
Language:English
Published: Korean Society of Anesthesiologists 2011-07-01
Series:Korean Journal of Anesthesiology
Subjects:
Online Access:http://ekja.org/upload/pdf/kjae-61-55.pdf
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author Yun Suk Choi
Seong-Ho Ok
Seung Min Lee
Sang-Seung Park
Yu Mi Ha
Ki Churl Chang
Hye Jung Kim
Il-Woo Shin
Ju-Tae Sohn
author_facet Yun Suk Choi
Seong-Ho Ok
Seung Min Lee
Sang-Seung Park
Yu Mi Ha
Ki Churl Chang
Hye Jung Kim
Il-Woo Shin
Ju-Tae Sohn
author_sort Yun Suk Choi
collection DOAJ
description BackgroundThe intravenous administration of indigo carmine has been reported to produce transiently increased blood pressure in patients. The goal of this in vitro study was to examine the effect of indigo carmine on phenylephrine-induced contractions in an isolated rat aorta and to determine the associated cellular mechanism with particular focus on the endothelium-derived vasodilators.MethodsThe concentration-response curves for phenylephrine were generated in the presence or absence of indigo carmine. Phenylephrine concentration-response curves were generated for the endothelium-intact rings pretreated independently with a nitric oxide synthase inhibitor, Nω-nitro-L-arginine methyl ester (L-NAME), a cyclooxygenase inhibitor, indomethacin, and a low-molecular-weight superoxide anion scavenger, tiron, in the presence or absence of indigo carmine. The fluorescence of oxidized dichlorofluorescein was measured in rat aortic vascular smooth muscle cells cultured in the control, indigo carmine alone and tiron plus indigo carmine.ResultsIndigo carmine (10-5 M) increased the phenylephrine-induced maximum contraction in the endothelium-intact rings with or without indomethacin, whereas indigo carmine produced a slight leftward shift in the phenylephrine concentration-response curves in the endothelium-denuded rings and L-NAME-pretreated endothelium-intact rings. In the endothelium-intact rings pretreated with tiron (10-2 M), indigo carmine did not alter phenylephrine concentration-response curves significantly. Indigo carmine (10-5 M) increased the fluorescence of oxidized dichlorofluorescein in the vascular smooth muscle cells, whereas tiron abolished the indigo carmine-induced increase in oxidized dichlorofluorescein fluorescence.ConclusionsIndigo carmine increases the phenylephrine-induced contraction mainly through an endothelium-dependent mechanism involving the inactivation of nitric oxide caused by the increased production of reactive oxygen species.
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spelling doaj.art-22b320659c5345689981fc470a97f57c2022-12-22T02:25:34ZengKorean Society of AnesthesiologistsKorean Journal of Anesthesiology2005-64192005-75632011-07-01611556210.4097/kjae.2011.61.1.557253Indigo carmine enhances phenylephrine-induced contractions in an isolated rat aortaYun Suk Choi0Seong-Ho Ok1Seung Min Lee2Sang-Seung Park3Yu Mi Ha4Ki Churl Chang5Hye Jung Kim6Il-Woo Shin7Ju-Tae Sohn8Department of Anesthesiology and Pain Medicine, Jeju National University School of Medicine, Jeju, Korea.Department of Anesthesiology and Pain Medicine, Gyeongsang National University School of Medicine, Jinju, Korea.Department of Anesthesiology and Pain Medicine, Gyeongsang National University School of Medicine, Jinju, Korea.Department of Anesthesiology and Pain Medicine, Gyeongsang National University School of Medicine, Jinju, Korea.Department of Pharmacology, Gyeongsang National University School of Medicine, Jinju, Korea.Department of Pharmacology, Gyeongsang National University School of Medicine, Jinju, Korea.Department of Pharmacology, Gyeongsang National University School of Medicine, Jinju, Korea.Department of Anesthesiology and Pain Medicine, Gyeongsang National University School of Medicine, Jinju, Korea.Department of Anesthesiology and Pain Medicine, Gyeongsang National University School of Medicine, Jinju, Korea.BackgroundThe intravenous administration of indigo carmine has been reported to produce transiently increased blood pressure in patients. The goal of this in vitro study was to examine the effect of indigo carmine on phenylephrine-induced contractions in an isolated rat aorta and to determine the associated cellular mechanism with particular focus on the endothelium-derived vasodilators.MethodsThe concentration-response curves for phenylephrine were generated in the presence or absence of indigo carmine. Phenylephrine concentration-response curves were generated for the endothelium-intact rings pretreated independently with a nitric oxide synthase inhibitor, Nω-nitro-L-arginine methyl ester (L-NAME), a cyclooxygenase inhibitor, indomethacin, and a low-molecular-weight superoxide anion scavenger, tiron, in the presence or absence of indigo carmine. The fluorescence of oxidized dichlorofluorescein was measured in rat aortic vascular smooth muscle cells cultured in the control, indigo carmine alone and tiron plus indigo carmine.ResultsIndigo carmine (10-5 M) increased the phenylephrine-induced maximum contraction in the endothelium-intact rings with or without indomethacin, whereas indigo carmine produced a slight leftward shift in the phenylephrine concentration-response curves in the endothelium-denuded rings and L-NAME-pretreated endothelium-intact rings. In the endothelium-intact rings pretreated with tiron (10-2 M), indigo carmine did not alter phenylephrine concentration-response curves significantly. Indigo carmine (10-5 M) increased the fluorescence of oxidized dichlorofluorescein in the vascular smooth muscle cells, whereas tiron abolished the indigo carmine-induced increase in oxidized dichlorofluorescein fluorescence.ConclusionsIndigo carmine increases the phenylephrine-induced contraction mainly through an endothelium-dependent mechanism involving the inactivation of nitric oxide caused by the increased production of reactive oxygen species.http://ekja.org/upload/pdf/kjae-61-55.pdfindigo carminenitric oxidephenylephrinereactive oxygen species
spellingShingle Yun Suk Choi
Seong-Ho Ok
Seung Min Lee
Sang-Seung Park
Yu Mi Ha
Ki Churl Chang
Hye Jung Kim
Il-Woo Shin
Ju-Tae Sohn
Indigo carmine enhances phenylephrine-induced contractions in an isolated rat aorta
Korean Journal of Anesthesiology
indigo carmine
nitric oxide
phenylephrine
reactive oxygen species
title Indigo carmine enhances phenylephrine-induced contractions in an isolated rat aorta
title_full Indigo carmine enhances phenylephrine-induced contractions in an isolated rat aorta
title_fullStr Indigo carmine enhances phenylephrine-induced contractions in an isolated rat aorta
title_full_unstemmed Indigo carmine enhances phenylephrine-induced contractions in an isolated rat aorta
title_short Indigo carmine enhances phenylephrine-induced contractions in an isolated rat aorta
title_sort indigo carmine enhances phenylephrine induced contractions in an isolated rat aorta
topic indigo carmine
nitric oxide
phenylephrine
reactive oxygen species
url http://ekja.org/upload/pdf/kjae-61-55.pdf
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