Matches in SemOpenAlex for { <https://semopenalex.org/work/W2904196891> ?p ?o ?g. }
- W2904196891 endingPage "2191" @default.
- W2904196891 startingPage "2183" @default.
- W2904196891 abstract "Objectives The aim of this study was to investigate the vascular effects and mechanisms of propofol in the human internal mammary artery (IMA). Design In vitro experimental study. Setting The study was conducted in the research laboratory of a pharmacology department. Participants IMA segments were obtained from 52 patients undergoing coronary artery bypass surgery. Interventions The IMA rings were suspended in isolated organ baths, and the changes in the tension were isometrically recorded. The antagonistic effect of propofol (1 μM, 10 μM, and 100 μM) on contractions induced by potassium chloride (45 mM), phenylephrine (1 μM), 5-hydroxytryptamine (30 μM), and calcium chloride (10 μM-10 mM) was investigated. The relaxations induced by propofol also were tested in the presence of the nitric oxide synthase inhibitor, nitro-L-arginine methyl ester (100 mM); the cyclooxygenase inhibitor, indomethacin (10 mM); and the potassium ion channel inhibitors, tetraethylammonium (1 mM), iberiotoxin (20 nM), glibenclamide (10 µM), 4-aminopyridine (1 mM), and barium chloride (30 µM). Measurements and Main Results Propofol caused a significant concentration-dependent vasorelaxation, which was endothelium independent. It inhibited the contractions induced by potassium chloride, phenylephrine, 5-hydroxytryptamine, and calcium chloride (p < 0.001), but it did not affect the basal tension. Propofol-induced relaxation was significantly inhibited by iberiotoxin and tetraethylammonium (p < 0.001); however, it was not affected by 4-aminopyridine, glibenclamide, and barium chloride. Conclusion This study clearly reveals that propofol relaxes the IMA, and propofol-induced vasodilation may be related to large conductance calcium ion–activated potassium ion channel activation. Propofol use in coronary artery bypass surgery can be valuable via its favorable vasodilator effect to overcome perioperative vasospasm of IMA. The aim of this study was to investigate the vascular effects and mechanisms of propofol in the human internal mammary artery (IMA). In vitro experimental study. The study was conducted in the research laboratory of a pharmacology department. IMA segments were obtained from 52 patients undergoing coronary artery bypass surgery. The IMA rings were suspended in isolated organ baths, and the changes in the tension were isometrically recorded. The antagonistic effect of propofol (1 μM, 10 μM, and 100 μM) on contractions induced by potassium chloride (45 mM), phenylephrine (1 μM), 5-hydroxytryptamine (30 μM), and calcium chloride (10 μM-10 mM) was investigated. The relaxations induced by propofol also were tested in the presence of the nitric oxide synthase inhibitor, nitro-L-arginine methyl ester (100 mM); the cyclooxygenase inhibitor, indomethacin (10 mM); and the potassium ion channel inhibitors, tetraethylammonium (1 mM), iberiotoxin (20 nM), glibenclamide (10 µM), 4-aminopyridine (1 mM), and barium chloride (30 µM). Propofol caused a significant concentration-dependent vasorelaxation, which was endothelium independent. It inhibited the contractions induced by potassium chloride, phenylephrine, 5-hydroxytryptamine, and calcium chloride (p < 0.001), but it did not affect the basal tension. Propofol-induced relaxation was significantly inhibited by iberiotoxin and tetraethylammonium (p < 0.001); however, it was not affected by 4-aminopyridine, glibenclamide, and barium chloride. This study clearly reveals that propofol relaxes the IMA, and propofol-induced vasodilation may be related to large conductance calcium ion–activated potassium ion channel activation. Propofol use in coronary artery bypass surgery can be valuable via its favorable vasodilator effect to overcome perioperative vasospasm of IMA." @default.
- W2904196891 created "2018-12-22" @default.
- W2904196891 creator A5017456516 @default.
- W2904196891 creator A5018084294 @default.
- W2904196891 creator A5019446966 @default.
- W2904196891 creator A5035863530 @default.
- W2904196891 creator A5081759504 @default.
- W2904196891 date "2019-08-01" @default.
- W2904196891 modified "2023-09-27" @default.
- W2904196891 title "Propofol-Induced Vasodilation in Human Internal Mammary Artery: Role of Potassium Channels" @default.
- W2904196891 cites W1967283178 @default.
- W2904196891 cites W1968249144 @default.
- W2904196891 cites W1968249854 @default.
- W2904196891 cites W1970096742 @default.
- W2904196891 cites W1970234267 @default.
- W2904196891 cites W1971169490 @default.
- W2904196891 cites W1980448073 @default.
- W2904196891 cites W1981964819 @default.
- W2904196891 cites W1987411006 @default.
- W2904196891 cites W1993180648 @default.
- W2904196891 cites W2002030087 @default.
- W2904196891 cites W2009323048 @default.
- W2904196891 cites W2015879989 @default.
- W2904196891 cites W2015924396 @default.
- W2904196891 cites W2021739695 @default.
- W2904196891 cites W2024254159 @default.
- W2904196891 cites W2025810352 @default.
- W2904196891 cites W2027477899 @default.
- W2904196891 cites W2034692827 @default.
- W2904196891 cites W2053518391 @default.
- W2904196891 cites W2060974177 @default.
- W2904196891 cites W2061817417 @default.
- W2904196891 cites W2064011840 @default.
- W2904196891 cites W2068832992 @default.
- W2904196891 cites W2085022918 @default.
- W2904196891 cites W2098963973 @default.
- W2904196891 cites W2100495345 @default.
- W2904196891 cites W2109750291 @default.
- W2904196891 cites W2110583919 @default.
- W2904196891 cites W2110922983 @default.
- W2904196891 cites W2129201273 @default.
- W2904196891 cites W2129774154 @default.
- W2904196891 cites W2135620964 @default.
- W2904196891 cites W2135936548 @default.
- W2904196891 cites W2146375752 @default.
- W2904196891 cites W2154617457 @default.
- W2904196891 cites W2158921063 @default.
- W2904196891 cites W2190671780 @default.
- W2904196891 cites W2207148293 @default.
- W2904196891 cites W2328447373 @default.
- W2904196891 cites W2520213510 @default.
- W2904196891 cites W2605870920 @default.
- W2904196891 cites W2769018017 @default.
- W2904196891 cites W2775470166 @default.
- W2904196891 cites W4255212921 @default.
- W2904196891 cites W4291746756 @default.
- W2904196891 cites W575337639 @default.
- W2904196891 doi "https://doi.org/10.1053/j.jvca.2018.12.015" @default.
- W2904196891 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30683593" @default.
- W2904196891 hasPublicationYear "2019" @default.
- W2904196891 type Work @default.
- W2904196891 sameAs 2904196891 @default.
- W2904196891 citedByCount "9" @default.
- W2904196891 countsByYear W29041968912019 @default.
- W2904196891 countsByYear W29041968912021 @default.
- W2904196891 countsByYear W29041968912022 @default.
- W2904196891 countsByYear W29041968912023 @default.
- W2904196891 crossrefType "journal-article" @default.
- W2904196891 hasAuthorship W2904196891A5017456516 @default.
- W2904196891 hasAuthorship W2904196891A5018084294 @default.
- W2904196891 hasAuthorship W2904196891A5019446966 @default.
- W2904196891 hasAuthorship W2904196891A5035863530 @default.
- W2904196891 hasAuthorship W2904196891A5081759504 @default.
- W2904196891 hasConcept C120770815 @default.
- W2904196891 hasConcept C126322002 @default.
- W2904196891 hasConcept C134018914 @default.
- W2904196891 hasConcept C178790620 @default.
- W2904196891 hasConcept C185592680 @default.
- W2904196891 hasConcept C2776277131 @default.
- W2904196891 hasConcept C2777952589 @default.
- W2904196891 hasConcept C2779411790 @default.
- W2904196891 hasConcept C2779768347 @default.
- W2904196891 hasConcept C2780918503 @default.
- W2904196891 hasConcept C2781295685 @default.
- W2904196891 hasConcept C42219234 @default.
- W2904196891 hasConcept C517785266 @default.
- W2904196891 hasConcept C555293320 @default.
- W2904196891 hasConcept C71924100 @default.
- W2904196891 hasConcept C83743174 @default.
- W2904196891 hasConcept C84393581 @default.
- W2904196891 hasConcept C98274493 @default.
- W2904196891 hasConceptScore W2904196891C120770815 @default.
- W2904196891 hasConceptScore W2904196891C126322002 @default.
- W2904196891 hasConceptScore W2904196891C134018914 @default.
- W2904196891 hasConceptScore W2904196891C178790620 @default.
- W2904196891 hasConceptScore W2904196891C185592680 @default.
- W2904196891 hasConceptScore W2904196891C2776277131 @default.
- W2904196891 hasConceptScore W2904196891C2777952589 @default.