The Journal of clinical endocrinology and metabolism · 2011
Cardioprotective effects of glucose and insulin administration while maintaining normoglycemia (GIN therapy) in patients undergoing coronary artery bypass grafting.
СтатьяРандомизированное исследованиеПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Carvalho George, Pelletier Patricia, Albacker Turki, Lachapelle Kevin, Joanisse Denis R, Hatzakorzian Roupen, Lattermann Ralph, Sato Hiroaki, Marette André, Schricker Thomas
Аннотация
CONTEXT: Coronary artery bypass grafting (CABG) is complicated by ischemia-reperfusion injury jeopardizing myocyte survival.
OBJECTIVE: The aim of the study was to investigate whether glucose and insulin administration, while maintaining normoglycemia (GIN therapy) using a hyperinsulinemic-normoglycemic clamp technique, is cardioprotective in patients undergoing CABG.
DESIGN AND SETTING: We conducted a randomized controlled trial at a tertiary care university teaching hospital.
PATIENTS: We studied 99 patients undergoing elective CABG.
INTERVENTION: Patients were randomly assigned to receive either GIN from the beginning of surgery until 24 h after CABG (GIN, n = 49) or standard metabolic care (control, n = 50).
MAIN OUTCOME MEASURES: We measured plasma concentrations of cardiac troponin I and free fatty acids, cardiac function as assessed by transesophageal echocardiography, glycogen content, glycogen synthase activity, and the expression of AMP-activated protein kinase (AMPK) and protein kinase B (AKT) in cardiomyocytes.
RESULTS: Patients receiving GIN therapy showed an attenuated release of cardiac troponin I (P < 0.05) and improved myocardial function (P < 0.05). Systemic free fatty acid concentrations were suppressed (P < 0.05), whereas intracellular glycogen content and glycogen synthase activity were not altered. The AMPK activity remained unchanged during ischemia in the GIN group, whereas it increased in the control group (P < 0.05). Enhanced AKT phosphorylation before ischemia was observed (P < 0.05) in the presence of GIN. However, there was no evidence for AKT-dependent AMPK inhibition.
CONCLUSIONS: GIN therapy protects the myocardium and inhibits ischemia-induced AMPK activation.
OBJECTIVE: The aim of the study was to investigate whether glucose and insulin administration, while maintaining normoglycemia (GIN therapy) using a hyperinsulinemic-normoglycemic clamp technique, is cardioprotective in patients undergoing CABG.
DESIGN AND SETTING: We conducted a randomized controlled trial at a tertiary care university teaching hospital.
PATIENTS: We studied 99 patients undergoing elective CABG.
INTERVENTION: Patients were randomly assigned to receive either GIN from the beginning of surgery until 24 h after CABG (GIN, n = 49) or standard metabolic care (control, n = 50).
MAIN OUTCOME MEASURES: We measured plasma concentrations of cardiac troponin I and free fatty acids, cardiac function as assessed by transesophageal echocardiography, glycogen content, glycogen synthase activity, and the expression of AMP-activated protein kinase (AMPK) and protein kinase B (AKT) in cardiomyocytes.
RESULTS: Patients receiving GIN therapy showed an attenuated release of cardiac troponin I (P < 0.05) and improved myocardial function (P < 0.05). Systemic free fatty acid concentrations were suppressed (P < 0.05), whereas intracellular glycogen content and glycogen synthase activity were not altered. The AMPK activity remained unchanged during ischemia in the GIN group, whereas it increased in the control group (P < 0.05). Enhanced AKT phosphorylation before ischemia was observed (P < 0.05) in the presence of GIN. However, there was no evidence for AKT-dependent AMPK inhibition.
CONCLUSIONS: GIN therapy protects the myocardium and inhibits ischemia-induced AMPK activation.
Предметные рубрики MeSH
AgedAnesthesiaBiopsyBlood GlucoseCardiotonic AgentsCoronary Artery BypassCyclic AMP-Dependent Protein KinasesEchocardiographyEnergy MetabolismFemaleGlucoseGlucose Clamp TechniqueGlycogenGlycogen SynthaseHumansHypoglycemic AgentsInsulinMaleMiddle AgedMuscle, SkeletalMyocardial Reperfusion InjuryMyocardial RevascularizationOncogene Protein v-aktPostoperative ComplicationsTreatment OutcomeTroponin C