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Moderate glucose supply reduces hemolysis during systemic inflammation

BACKGROUND: Systemic inflammation alters energy metabolism. A sufficient glucose level, however, is most important for erythrocytes, since erythrocytes rely on glucose as sole source of energy. Damage to erythrocytes leads to hemolysis. Both disorders of glucose metabolism and hemolysis are associat...

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Autores principales: Jägers, Johannes, Brauckmann, Stephan, Kirsch, Michael, Effenberger-Neidnicht, Katharina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856073/
https://www.ncbi.nlm.nih.gov/pubmed/29559805
http://dx.doi.org/10.2147/JIR.S155614
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author Jägers, Johannes
Brauckmann, Stephan
Kirsch, Michael
Effenberger-Neidnicht, Katharina
author_facet Jägers, Johannes
Brauckmann, Stephan
Kirsch, Michael
Effenberger-Neidnicht, Katharina
author_sort Jägers, Johannes
collection PubMed
description BACKGROUND: Systemic inflammation alters energy metabolism. A sufficient glucose level, however, is most important for erythrocytes, since erythrocytes rely on glucose as sole source of energy. Damage to erythrocytes leads to hemolysis. Both disorders of glucose metabolism and hemolysis are associated with an increased risk of death. The objective of the study was to investigate the impact of intravenous glucose on hemolysis during systemic inflammation. MATERIALS AND METHODS: Systemic inflammation was accomplished in male Wistar rats by continuous lipopolysaccharide (LPS) infusion (1 mg LPS/kg and h, 300 min). Sham control group rats received Ringer’s solution. Glucose was supplied moderately (70 mg glucose/kg and h) or excessively (210 mg glucose/kg and h) during systemic inflammation. Vital parameters (eg, systemic blood pressure) as well as blood and plasma parameters (eg, concentrations of glucose, lactate and cell-free hemoglobin, and activity of lactate dehydrogenase) were measured hourly. Clot formation was analyzed by thromboelastometry. RESULTS: Continuous infusion of LPS led to a so-called post-aggression syndrome with disturbed electrolyte homeostasis (hypocalcemia, hyperkalemia, and hypernatremia), changes in hemodynamics (tachycardia and hypertension), and a catabolic metabolism (early hyperglycemia, late hypoglycemia, and lactate formation). It induced severe tissue injury (significant increases in plasma concentrations of transaminases and lactate dehydrogenase), alterations in blood coagulation (disturbed clot formation), and massive hemolysis. Both moderate and excessive glucose supply reduced LPS-induced increase in systemic blood pressure. Excessive but not moderate glucose supply increased blood glucose level and enhanced tissue injury. Glucose supply did not reduce LPS-induced alterations in coagulation, but significantly reduced hemolysis induced by LPS. CONCLUSION: Intravenous glucose infusion can diminish LPS-related changes in hemodynamics, glucose metabolism, and, more interestingly, LPS-induced hemolysis. Since cell-free hemoglobin is known to be a predictor for patient’s survival, a reduction of hemolysis by 35% only by the addition of a small amount of glucose is another step to minimize mortality during systemic inflammation.
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spelling pubmed-58560732018-03-20 Moderate glucose supply reduces hemolysis during systemic inflammation Jägers, Johannes Brauckmann, Stephan Kirsch, Michael Effenberger-Neidnicht, Katharina J Inflamm Res Original Research BACKGROUND: Systemic inflammation alters energy metabolism. A sufficient glucose level, however, is most important for erythrocytes, since erythrocytes rely on glucose as sole source of energy. Damage to erythrocytes leads to hemolysis. Both disorders of glucose metabolism and hemolysis are associated with an increased risk of death. The objective of the study was to investigate the impact of intravenous glucose on hemolysis during systemic inflammation. MATERIALS AND METHODS: Systemic inflammation was accomplished in male Wistar rats by continuous lipopolysaccharide (LPS) infusion (1 mg LPS/kg and h, 300 min). Sham control group rats received Ringer’s solution. Glucose was supplied moderately (70 mg glucose/kg and h) or excessively (210 mg glucose/kg and h) during systemic inflammation. Vital parameters (eg, systemic blood pressure) as well as blood and plasma parameters (eg, concentrations of glucose, lactate and cell-free hemoglobin, and activity of lactate dehydrogenase) were measured hourly. Clot formation was analyzed by thromboelastometry. RESULTS: Continuous infusion of LPS led to a so-called post-aggression syndrome with disturbed electrolyte homeostasis (hypocalcemia, hyperkalemia, and hypernatremia), changes in hemodynamics (tachycardia and hypertension), and a catabolic metabolism (early hyperglycemia, late hypoglycemia, and lactate formation). It induced severe tissue injury (significant increases in plasma concentrations of transaminases and lactate dehydrogenase), alterations in blood coagulation (disturbed clot formation), and massive hemolysis. Both moderate and excessive glucose supply reduced LPS-induced increase in systemic blood pressure. Excessive but not moderate glucose supply increased blood glucose level and enhanced tissue injury. Glucose supply did not reduce LPS-induced alterations in coagulation, but significantly reduced hemolysis induced by LPS. CONCLUSION: Intravenous glucose infusion can diminish LPS-related changes in hemodynamics, glucose metabolism, and, more interestingly, LPS-induced hemolysis. Since cell-free hemoglobin is known to be a predictor for patient’s survival, a reduction of hemolysis by 35% only by the addition of a small amount of glucose is another step to minimize mortality during systemic inflammation. Dove Medical Press 2018-03-12 /pmc/articles/PMC5856073/ /pubmed/29559805 http://dx.doi.org/10.2147/JIR.S155614 Text en © 2018 Jägers et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Jägers, Johannes
Brauckmann, Stephan
Kirsch, Michael
Effenberger-Neidnicht, Katharina
Moderate glucose supply reduces hemolysis during systemic inflammation
title Moderate glucose supply reduces hemolysis during systemic inflammation
title_full Moderate glucose supply reduces hemolysis during systemic inflammation
title_fullStr Moderate glucose supply reduces hemolysis during systemic inflammation
title_full_unstemmed Moderate glucose supply reduces hemolysis during systemic inflammation
title_short Moderate glucose supply reduces hemolysis during systemic inflammation
title_sort moderate glucose supply reduces hemolysis during systemic inflammation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856073/
https://www.ncbi.nlm.nih.gov/pubmed/29559805
http://dx.doi.org/10.2147/JIR.S155614
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