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dc.contributor.authorBagcivan, Ihsan
dc.contributor.authorGursoy, Sinan
dc.contributor.authorYildirim, M. Kemal
dc.contributor.authorTemiz, Tijen Kaya
dc.contributor.authorYildirim, Sahin
dc.contributor.authorYilmaz, Abdulkerim
dc.contributor.authorTuran, Mustafa
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:17:28Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:17:28Z
dc.date.issued2007
dc.identifier.issn1424-3903
dc.identifier.urihttps://dx.doi.org/10.1159/000104242
dc.identifier.urihttps://hdl.handle.net/20.500.12418/10727
dc.descriptionWOS: 000248240900012en_US
dc.descriptionPubMed ID: 17592231en_US
dc.description.abstractBackground/Aims: Intravenous anesthetics are often used for conscious sedation in endoscopic retrograde cholangio-pancreatography ( ERCP) and endoscopic sphincter of Oddi ( SO) manometry. This study was designed to investigate the effects of propofol on sheep SO. Methods: SO rings were mounted in a tissue bath and tested for changes in isometric tension in response to propofol (10(-8)-10(-4) M) in the presence or absence of L - NAME (3 X 10(-5) M), a non-specific inhibitor of nitric oxide (NO) synthase; indomethacin (10(-5) M), an inhibitor of cyclooxygenase; glibenclamide (10(-5) M), an inhibitor of ATP-sensitive potassium channels; tetraethylammonium (3 X 10(-4) M), inhibitors of calcium-activated potassium channels; 4-aminopyridine (10(-3) M), a voltage-dependent potassium channel blocker. Furthermore, we investigated the Ca2+ antagonist feature of propofol in precontracted SO rings by CaCl2. Results: Carbachol (10(-9)-10(-5) M) induced concentration-dependent contraction responses in the SO rings. Propofol (10(-8)-10(-4) M) produced concentration-dependent relaxation on isolated SO rings precontracted by carbachol (10(-6) M). Preincubation of SO rings by L - NAME ( 3 X 10(-5) M), indomethacin (10(-5) M), glibenclamide (10(-5) M), and 4-amino-pyridine (10(-3) M) did not produce a significant alteration on propofol-induced relaxation responses (p > 0.05), while preincubation by tetraethylammonium ( 3 X 10(-4) M) significantly decreased the propofol-induced relaxation responses (p < 0.05). Propofol (10(-8)-10(-4) M) induced concentration-dependently relaxations in precontracted isolated SO rings by CaCl2. Conclusion: The results suggest that propofol induced concentration-dependent relaxations in precontracted isolated SO rings. These relaxations are independent from NO, cyclooxygenase metabolites, and opened ATP-sensitive and voltage-dependent potassium channels. Opened Ca2+-sensitive K+ channels and inhibited L- type Ca2+ channels existing in smooth muscle by propofol can contribute to these relaxations. Propofol can be beneficial as alternative drugs for obtaining selective relaxation during SO manometry after controlled clinical studies. Copyright (c) 2007 S. Karger AG, Basel and IAP.en_US
dc.language.isoengen_US
dc.publisherKARGERen_US
dc.relation.isversionof10.1159/000104242en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectpropofolen_US
dc.subjectsphincter of Oddien_US
dc.subjectrelaxationen_US
dc.subjectsheepen_US
dc.titleInvestigation of relaxant effects of propofol on sheep sphincter of Oddien_US
dc.typearticleen_US
dc.relation.journalPANCREATOLOGYen_US
dc.contributor.departmentCumhuriyet Univ Sch Med, Dept Pharmacol, TR-58140 Sivas, Turkey -- Cumhuriyet Univ Sch Med, Dept Anesthesiol, TR-58140 Sivas, Turkey -- Cumhuriyet Univ Sch Med, Dept Internal Med, TR-58140 Sivas, Turkey -- Universal Hosp Grp, German Hosp, Dept Gen Surg, Istanbul, Turkeyen_US
dc.identifier.volume7en_US
dc.identifier.issue02.Maren_US
dc.identifier.endpage179en_US
dc.identifier.startpage174en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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