The Concentration-Dependent Contractile Effect of Methylene Blue in the Human Internal Mammary Artery: A Quantitative Approach to Its Use in the Vasoplegic Syndrome

Objective: To quantitate the contractile effect of methylene blue on isolated human internal mammary artery (IMA) as used in the vasoplegic syndrome. Design: An in vitro experimental study. Setting: Cardiovascular Pharmacology Laboratory, Department of Medical Pharmacology. Participants: IMA segment...

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Veröffentlicht in:Journal of cardiothoracic and vascular anesthesia 2008-08, Vol.22 (4), p.560-564
Hauptverfasser: Ulusoy, Hasan B., MD, PhD, Gul, Husamettin, MD, PhD, Seyrek, Melik, MD, PhD, Yildiz, Oguzhan, MD, PhD, Ulku, Cunay, MD, PhD, Yıldırım, Vedat, MD, Kuralay, Erkan, MD, Celik, Turgay, MD, Yanarates, Omer, MD
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container_end_page 564
container_issue 4
container_start_page 560
container_title Journal of cardiothoracic and vascular anesthesia
container_volume 22
creator Ulusoy, Hasan B., MD, PhD
Gul, Husamettin, MD, PhD
Seyrek, Melik, MD, PhD
Yildiz, Oguzhan, MD, PhD
Ulku, Cunay, MD, PhD
Yıldırım, Vedat, MD
Kuralay, Erkan, MD
Celik, Turgay, MD
Yanarates, Omer, MD
description Objective: To quantitate the contractile effect of methylene blue on isolated human internal mammary artery (IMA) as used in the vasoplegic syndrome. Design: An in vitro experimental study. Setting: Cardiovascular Pharmacology Laboratory, Department of Medical Pharmacology. Participants: IMA segments were used from 24 patients undergoing coronary artery bypass surgery. Interventions: The responses to methylene blue, norepinephrine, and acetylcholine were recorded isometrically by a force-displacement transducer in an isolated organ bath. Measurement and Main Results: Methylene blue (10 nmol/L-100 μmol/L) produced concentration-dependent contraction in the arteries. The maximal contraction to methylene blue was 44.2% ± 3.8% of KCl (68 mmol/L) maximum contraction; the pEC50 (−log10 of 50% effective concentration) value was 5.5 ± 0.1. Methylene blue caused an insignificant leftward shift of the concentration-response curve of norepinephrine. Acetylcholine-induced relaxation in submaximal contracted rings with phenylephrine recovered nearly 6 hours after the methylene blue challenge. Conclusion: Methylene blue caused concentration-dependent contraction in human IMAs. Furthermore, the inhibition of ACh-induced relaxation for 6 hours after the methylene blue challenge points out an additional mechanism (ie, receptor occupation). The concentration-dependent contractile effect of methylene blue justifies its use in the vasoplegic syndrome. The findings also suggest that the time course of contraction is longer than the exposure to methylene blue.
doi_str_mv 10.1053/j.jvca.2008.02.018
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Design: An in vitro experimental study. Setting: Cardiovascular Pharmacology Laboratory, Department of Medical Pharmacology. Participants: IMA segments were used from 24 patients undergoing coronary artery bypass surgery. Interventions: The responses to methylene blue, norepinephrine, and acetylcholine were recorded isometrically by a force-displacement transducer in an isolated organ bath. Measurement and Main Results: Methylene blue (10 nmol/L-100 μmol/L) produced concentration-dependent contraction in the arteries. The maximal contraction to methylene blue was 44.2% ± 3.8% of KCl (68 mmol/L) maximum contraction; the pEC50 (−log10 of 50% effective concentration) value was 5.5 ± 0.1. Methylene blue caused an insignificant leftward shift of the concentration-response curve of norepinephrine. Acetylcholine-induced relaxation in submaximal contracted rings with phenylephrine recovered nearly 6 hours after the methylene blue challenge. Conclusion: Methylene blue caused concentration-dependent contraction in human IMAs. Furthermore, the inhibition of ACh-induced relaxation for 6 hours after the methylene blue challenge points out an additional mechanism (ie, receptor occupation). The concentration-dependent contractile effect of methylene blue justifies its use in the vasoplegic syndrome. The findings also suggest that the time course of contraction is longer than the exposure to methylene blue.</description><identifier>ISSN: 1053-0770</identifier><identifier>EISSN: 1532-8422</identifier><identifier>DOI: 10.1053/j.jvca.2008.02.018</identifier><identifier>PMID: 18662631</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Anesthesia &amp; Perioperative Care ; contraction ; Critical Care ; Dose-Response Relationship, Drug ; human internal mammary artery ; Humans ; In Vitro Techniques ; Mammary Arteries - drug effects ; Mammary Arteries - physiology ; methylene blue ; Methylene Blue - administration &amp; dosage ; Middle Aged ; Muscle Contraction - drug effects ; Muscle Contraction - physiology ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - physiology ; Syndrome ; Vasoconstriction - drug effects ; Vasoconstriction - physiology ; vasoplegic syndrome</subject><ispartof>Journal of cardiothoracic and vascular anesthesia, 2008-08, Vol.22 (4), p.560-564</ispartof><rights>Elsevier Inc.</rights><rights>2008 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-e92d971889fff7513fd758c3fb99a2d020be15728c8a8b3a550e536331ee00743</citedby><cites>FETCH-LOGICAL-c409t-e92d971889fff7513fd758c3fb99a2d020be15728c8a8b3a550e536331ee00743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1053077008000505$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18662631$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ulusoy, Hasan B., MD, PhD</creatorcontrib><creatorcontrib>Gul, Husamettin, MD, PhD</creatorcontrib><creatorcontrib>Seyrek, Melik, MD, PhD</creatorcontrib><creatorcontrib>Yildiz, Oguzhan, MD, PhD</creatorcontrib><creatorcontrib>Ulku, Cunay, MD, PhD</creatorcontrib><creatorcontrib>Yıldırım, Vedat, MD</creatorcontrib><creatorcontrib>Kuralay, Erkan, MD</creatorcontrib><creatorcontrib>Celik, Turgay, MD</creatorcontrib><creatorcontrib>Yanarates, Omer, MD</creatorcontrib><title>The Concentration-Dependent Contractile Effect of Methylene Blue in the Human Internal Mammary Artery: A Quantitative Approach to Its Use in the Vasoplegic Syndrome</title><title>Journal of cardiothoracic and vascular anesthesia</title><addtitle>J Cardiothorac Vasc Anesth</addtitle><description>Objective: To quantitate the contractile effect of methylene blue on isolated human internal mammary artery (IMA) as used in the vasoplegic syndrome. 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Conclusion: Methylene blue caused concentration-dependent contraction in human IMAs. Furthermore, the inhibition of ACh-induced relaxation for 6 hours after the methylene blue challenge points out an additional mechanism (ie, receptor occupation). The concentration-dependent contractile effect of methylene blue justifies its use in the vasoplegic syndrome. The findings also suggest that the time course of contraction is longer than the exposure to methylene blue.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18662631</pmid><doi>10.1053/j.jvca.2008.02.018</doi><tpages>5</tpages></addata></record>
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subjects Adult
Aged
Anesthesia & Perioperative Care
contraction
Critical Care
Dose-Response Relationship, Drug
human internal mammary artery
Humans
In Vitro Techniques
Mammary Arteries - drug effects
Mammary Arteries - physiology
methylene blue
Methylene Blue - administration & dosage
Middle Aged
Muscle Contraction - drug effects
Muscle Contraction - physiology
Muscle, Smooth, Vascular - drug effects
Muscle, Smooth, Vascular - physiology
Syndrome
Vasoconstriction - drug effects
Vasoconstriction - physiology
vasoplegic syndrome
title The Concentration-Dependent Contractile Effect of Methylene Blue in the Human Internal Mammary Artery: A Quantitative Approach to Its Use in the Vasoplegic Syndrome
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