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Der positiv inotrope Effekt von Insulin am menschlichen Myokard

dc.contributor.advisorWachter, Rolf Prof. Dr.
dc.contributor.authorKania, Sebastian Martin Albert
dc.date.accessioned2016-06-09T07:30:29Z
dc.date.available2016-07-06T22:50:06Z
dc.date.issued2016-06-09
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-0028-8773-0
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-5682
dc.language.isodeude
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc610de
dc.titleDer positiv inotrope Effekt von Insulin am menschlichen Myokardde
dc.typedoctoralThesisde
dc.title.translatedThe positive inotropic effect of insulin on human myocardiumde
dc.contributor.refereeZimmermann, Wolfram-Hubertus Prof. Dr.
dc.date.examination2016-06-29
dc.description.abstractengInsulin has been shown to exert positive inotropic effects in several in vitro and in vivo models, but signal transduction and substrate dependency remain unclear. We examined inotropic responses and signal transduction mechanisms of insulin in human myocardium. Experiments were performed in isolated trabeculae from end-stage failing hearts of 58 nondiabetic and 3 diabetic patients undergoing heart transplantation. The effect of insulin (0.3 and 3 IU/L) on isometric twitch force (37 degrees C, 1 Hz) was tested in the presence of glucose or pyruvate as energetic substrate. Furthermore, intracellular Ca2+ transients (aequorin method), sarcoplasmic reticulum (SR) Ca2+ content (rapid cooling contractures), and myofilament Ca2+ sensitivity (semiskinned fibers) were assessed. In addition, potential signaling pathways were tested by blocking glycolysis, PI-3-kinase, protein kinase C, diacylglycerol kinase, insulin-like growth factor-1 receptors, or transsarcolemmal Ca2+ entry via the Na+/Ca2+ exchanger. Insulin exerted concentration-dependent and partially substrate-dependent positive inotropic effects. The phosphatidylinositol-3-kinase inhibitor wortmannin and the Na2+/Ca2+ exchanger reverse-mode inhibitor KB-R7943 completely or partially prevented the functional effects of insulin. In contrast, insulin-like growth factor-1 receptor blockade, protein kinase C inhibition, and diacylglycerol kinase blockade were without effect. The inotropic response was associated with increases in intracellular Ca2+ transients, SR Ca2+ content, and increased myofilament Ca2+ sensitivity.Insulin exerts Ca2+-dependent and -independent positive inotropic effects through a phosphatidylinositol-3-kinase-dependent pathway in failing human myocardium. The increased [Ca2+]i originates at least in part from enhanced reverse-mode Na+/Ca2+ exchange and consequently increased SR-Ca2+ load. These nongenomic functional effects of insulin may be of clinical relevance, eg, during insulin-glucose-potassium infusions.de
dc.contributor.coRefereeKrick, Wolfgang PD Dr.
dc.subject.gerInsulinde
dc.subject.gerMyokardde
dc.subject.gerInotropiede
dc.subject.gerSignaltransductionde
dc.subject.gerKlaziumtransientde
dc.subject.gerKalziumde
dc.subject.gerPI-3-Kinasede
dc.subject.gerPyruvatde
dc.subject.engInsulinde
dc.subject.engmyocardiumde
dc.subject.enginotropic responsede
dc.subject.engsignaltransductionde
dc.subject.engPI-3-Kinasede
dc.subject.engcalciumtransientde
dc.subject.engpyruvatede
dc.subject.engCalciumde
dc.identifier.urnurn:nbn:de:gbv:7-11858/00-1735-0000-0028-8773-0-6
dc.affiliation.instituteMedizinische Fakultätde
dc.subject.gokfullInnere Medizin - Allgemein- und Gesamtdarstellungen (PPN619875747)de
dc.description.embargoed2016-07-06
dc.identifier.ppn860833372


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