Cargando…

Depletion of myocardial glucose is observed during endotoxemic but not hemorrhagic shock in a porcine model

INTRODUCTION: Metabolic dysfunction is one of the hallmarks of sepsis yet little is known about local changes in key organs such as the heart. The aim of this study was to compare myocardial metabolic changes by direct measurements of substrates, such as glucose, lactate and pyruvate, using microdia...

Descripción completa

Detalles Bibliográficos
Autores principales: Chew, Michelle S, Shekar, Kiran, Brand, Björn A, Norin, Carl, Barnett, Adrian G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231428/
https://www.ncbi.nlm.nih.gov/pubmed/23886047
http://dx.doi.org/10.1186/cc12843
_version_ 1782344443340259328
author Chew, Michelle S
Shekar, Kiran
Brand, Björn A
Norin, Carl
Barnett, Adrian G
author_facet Chew, Michelle S
Shekar, Kiran
Brand, Björn A
Norin, Carl
Barnett, Adrian G
author_sort Chew, Michelle S
collection PubMed
description INTRODUCTION: Metabolic dysfunction is one of the hallmarks of sepsis yet little is known about local changes in key organs such as the heart. The aim of this study was to compare myocardial metabolic changes by direct measurements of substrates, such as glucose, lactate and pyruvate, using microdialysis (MD) in in-vivo porcine endotoxemic and hemorrhagic shock. To assess whether these changes were specific to the heart, we simultaneously investigated substrate levels in skeletal muscle. METHODS: Twenty-six female pigs were randomized to three groups: control (C) n = 8, endotoxemic shock (E) n = 9 and hemorrhagic shock (H) n = 9. Interstitial myocardial pyruvate, lactate and glucose were measured using MD. Skeletal muscle MD was also performed in all three groups. RESULTS: Marked decreases in myocardial glucose were observed in the E group but not in the H group compared to controls (mean difference (CI) in mmol/L: C versus E -1.5(-2.2 to -0.8), P <0.001; H versus E -1.1(-1.8 to -0.4), P = 0.004; C versus H -0.4(-1.1 to 0.3), P = 0.282). Up to four-fold increases in myocardial pyruvate and three-fold increases in lactate were seen in both shock groups with no differences between the two types of shock. There was no evidence of myocardial anaerobic metabolism, with normal lactate:pyruvate (L:P) ratios seen in all animals regardless of the type of shock. In skeletal muscle, decreases in glucose concentrations were observed in the E group only (mean difference: C versus E -0.8(-1.4 to -0.3), P = 0.007). Although skeletal muscle lactate increased in both shock groups, this was accompanied by increases in pyruvate in the E group only (mean difference: C versus E 121(46 to 195), P = 0.003; H versus E 77(7 to 147), P = 0.032; C versus H 43(-30 to 43), P = 0.229). The L:P ratio was increased in skeletal muscle in response to hemorrhagic, but not endotoxemic, shock. CONCLUSIONS: Endotoxemia, but not hemorrhage, induces a rapid decrease of myocardial glucose levels. Despite the decrease in glucose, myocardial lactate and pyruvate concentrations were elevated and not different than in hemorrhagic shock. In skeletal muscle, substrate patterns during endotoxemic shock mimicked those seen in myocardium. During hemorrhagic shock the skeletal muscle response was characterized by a lack of increase in pyruvate and higher L:P ratios. Hence, metabolic patterns in the myocardium during endotoxemic shock are different than those seen during hemorrhagic shock. Skeletal muscle and myocardium displayed similar substrate patterns during endotoxemic shock but differed during hemorrhagic shock.
format Online
Article
Text
id pubmed-4231428
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-42314282014-11-15 Depletion of myocardial glucose is observed during endotoxemic but not hemorrhagic shock in a porcine model Chew, Michelle S Shekar, Kiran Brand, Björn A Norin, Carl Barnett, Adrian G Crit Care Research INTRODUCTION: Metabolic dysfunction is one of the hallmarks of sepsis yet little is known about local changes in key organs such as the heart. The aim of this study was to compare myocardial metabolic changes by direct measurements of substrates, such as glucose, lactate and pyruvate, using microdialysis (MD) in in-vivo porcine endotoxemic and hemorrhagic shock. To assess whether these changes were specific to the heart, we simultaneously investigated substrate levels in skeletal muscle. METHODS: Twenty-six female pigs were randomized to three groups: control (C) n = 8, endotoxemic shock (E) n = 9 and hemorrhagic shock (H) n = 9. Interstitial myocardial pyruvate, lactate and glucose were measured using MD. Skeletal muscle MD was also performed in all three groups. RESULTS: Marked decreases in myocardial glucose were observed in the E group but not in the H group compared to controls (mean difference (CI) in mmol/L: C versus E -1.5(-2.2 to -0.8), P <0.001; H versus E -1.1(-1.8 to -0.4), P = 0.004; C versus H -0.4(-1.1 to 0.3), P = 0.282). Up to four-fold increases in myocardial pyruvate and three-fold increases in lactate were seen in both shock groups with no differences between the two types of shock. There was no evidence of myocardial anaerobic metabolism, with normal lactate:pyruvate (L:P) ratios seen in all animals regardless of the type of shock. In skeletal muscle, decreases in glucose concentrations were observed in the E group only (mean difference: C versus E -0.8(-1.4 to -0.3), P = 0.007). Although skeletal muscle lactate increased in both shock groups, this was accompanied by increases in pyruvate in the E group only (mean difference: C versus E 121(46 to 195), P = 0.003; H versus E 77(7 to 147), P = 0.032; C versus H 43(-30 to 43), P = 0.229). The L:P ratio was increased in skeletal muscle in response to hemorrhagic, but not endotoxemic, shock. CONCLUSIONS: Endotoxemia, but not hemorrhage, induces a rapid decrease of myocardial glucose levels. Despite the decrease in glucose, myocardial lactate and pyruvate concentrations were elevated and not different than in hemorrhagic shock. In skeletal muscle, substrate patterns during endotoxemic shock mimicked those seen in myocardium. During hemorrhagic shock the skeletal muscle response was characterized by a lack of increase in pyruvate and higher L:P ratios. Hence, metabolic patterns in the myocardium during endotoxemic shock are different than those seen during hemorrhagic shock. Skeletal muscle and myocardium displayed similar substrate patterns during endotoxemic shock but differed during hemorrhagic shock. BioMed Central 2013 2013-07-25 /pmc/articles/PMC4231428/ /pubmed/23886047 http://dx.doi.org/10.1186/cc12843 Text en Copyright © 2013 Chew et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Chew, Michelle S
Shekar, Kiran
Brand, Björn A
Norin, Carl
Barnett, Adrian G
Depletion of myocardial glucose is observed during endotoxemic but not hemorrhagic shock in a porcine model
title Depletion of myocardial glucose is observed during endotoxemic but not hemorrhagic shock in a porcine model
title_full Depletion of myocardial glucose is observed during endotoxemic but not hemorrhagic shock in a porcine model
title_fullStr Depletion of myocardial glucose is observed during endotoxemic but not hemorrhagic shock in a porcine model
title_full_unstemmed Depletion of myocardial glucose is observed during endotoxemic but not hemorrhagic shock in a porcine model
title_short Depletion of myocardial glucose is observed during endotoxemic but not hemorrhagic shock in a porcine model
title_sort depletion of myocardial glucose is observed during endotoxemic but not hemorrhagic shock in a porcine model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231428/
https://www.ncbi.nlm.nih.gov/pubmed/23886047
http://dx.doi.org/10.1186/cc12843
work_keys_str_mv AT chewmichelles depletionofmyocardialglucoseisobservedduringendotoxemicbutnothemorrhagicshockinaporcinemodel
AT shekarkiran depletionofmyocardialglucoseisobservedduringendotoxemicbutnothemorrhagicshockinaporcinemodel
AT brandbjorna depletionofmyocardialglucoseisobservedduringendotoxemicbutnothemorrhagicshockinaporcinemodel
AT norincarl depletionofmyocardialglucoseisobservedduringendotoxemicbutnothemorrhagicshockinaporcinemodel
AT barnettadriang depletionofmyocardialglucoseisobservedduringendotoxemicbutnothemorrhagicshockinaporcinemodel