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Metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs

INTRODUCTION: Hepatic mitochondrial dysfunction may play a critical role in the pathogenesis of metformin-induced lactic acidosis. However, patients with severe metformin intoxication may have a 30 to 60% decrease in their global oxygen consumption, as for generalized inhibition of mitochondrial res...

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Autores principales: Protti, Alessandro, Fortunato, Francesco, Monti, Massimo, Vecchio, Sarah, Gatti, Stefano, Comi, Giacomo P, De Giuseppe, Rachele, Gattinoni, Luciano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580617/
https://www.ncbi.nlm.nih.gov/pubmed/22568883
http://dx.doi.org/10.1186/cc11332
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author Protti, Alessandro
Fortunato, Francesco
Monti, Massimo
Vecchio, Sarah
Gatti, Stefano
Comi, Giacomo P
De Giuseppe, Rachele
Gattinoni, Luciano
author_facet Protti, Alessandro
Fortunato, Francesco
Monti, Massimo
Vecchio, Sarah
Gatti, Stefano
Comi, Giacomo P
De Giuseppe, Rachele
Gattinoni, Luciano
author_sort Protti, Alessandro
collection PubMed
description INTRODUCTION: Hepatic mitochondrial dysfunction may play a critical role in the pathogenesis of metformin-induced lactic acidosis. However, patients with severe metformin intoxication may have a 30 to 60% decrease in their global oxygen consumption, as for generalized inhibition of mitochondrial respiration. We developed a pig model of severe metformin intoxication to validate this clinical finding and assess mitochondrial function in liver and other tissues. METHODS: Twenty healthy pigs were sedated and mechanically ventilated. Ten were infused with a large dose of metformin (4 to 8 g) and five were not (sham controls). Five others were infused with lactic acid to clarify whether lactic acidosis per se diminishes global oxygen use. Arterial pH, lactatemia, global oxygen consumption (VO(2)) (metabolic module) and delivery (DO(2)) (cardiac output by thermodilution) were monitored for nine hours. Oxygen extraction was computed as VO(2)/DO(2). Activities of the main components of the mitochondrial respiratory chain (complex I, II and III, and IV) were measured with spectrophotometry (and expressed relative to citrate synthase activity) in heart, kidney, liver, skeletal muscle and platelets taken at the end of the study. RESULTS: Pigs infused with metformin (6 ± 2 g; final serum drug level 77 ± 45 mg/L) progressively developed lactic acidosis (final arterial pH 6.93 ± 0.24 and lactate 18 ± 7 mmol/L, P < 0.001 for both). Their VO(2 )declined over time (from 115 ± 34 to 71 ± 30 ml/min, P < 0.001) despite grossly preserved DO(2 )(from 269 ± 68 to 239 ± 51 ml/min, P = 0.58). Oxygen extraction accordingly fell from 43 ± 10 to 30 ± 10% (P = 0.008). None of these changes occurred in either sham controls or pigs infused with lactic acid (final arterial pH 6.86 ± 0.16 and lactate 22 ± 3 mmol/L). Metformin intoxication was associated with inhibition of complex I in the liver (P < 0.001), heart (P < 0.001), kidney (P = 0.003), skeletal muscle (P = 0.012) and platelets (P = 0.053). The activity of complex II and III diminished in the liver (P < 0.001), heart (P < 0.001) and kidney (P < 0.005) while that of complex IV declined in the heart (P < 0.001). CONCLUSIONS: Metformin intoxication induces lactic acidosis, inhibits global oxygen consumption and causes mitochondrial dysfunction in liver and other tissues. Lactic acidosis per se does not decrease whole-body respiration.
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spelling pubmed-35806172013-02-26 Metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs Protti, Alessandro Fortunato, Francesco Monti, Massimo Vecchio, Sarah Gatti, Stefano Comi, Giacomo P De Giuseppe, Rachele Gattinoni, Luciano Crit Care Research INTRODUCTION: Hepatic mitochondrial dysfunction may play a critical role in the pathogenesis of metformin-induced lactic acidosis. However, patients with severe metformin intoxication may have a 30 to 60% decrease in their global oxygen consumption, as for generalized inhibition of mitochondrial respiration. We developed a pig model of severe metformin intoxication to validate this clinical finding and assess mitochondrial function in liver and other tissues. METHODS: Twenty healthy pigs were sedated and mechanically ventilated. Ten were infused with a large dose of metformin (4 to 8 g) and five were not (sham controls). Five others were infused with lactic acid to clarify whether lactic acidosis per se diminishes global oxygen use. Arterial pH, lactatemia, global oxygen consumption (VO(2)) (metabolic module) and delivery (DO(2)) (cardiac output by thermodilution) were monitored for nine hours. Oxygen extraction was computed as VO(2)/DO(2). Activities of the main components of the mitochondrial respiratory chain (complex I, II and III, and IV) were measured with spectrophotometry (and expressed relative to citrate synthase activity) in heart, kidney, liver, skeletal muscle and platelets taken at the end of the study. RESULTS: Pigs infused with metformin (6 ± 2 g; final serum drug level 77 ± 45 mg/L) progressively developed lactic acidosis (final arterial pH 6.93 ± 0.24 and lactate 18 ± 7 mmol/L, P < 0.001 for both). Their VO(2 )declined over time (from 115 ± 34 to 71 ± 30 ml/min, P < 0.001) despite grossly preserved DO(2 )(from 269 ± 68 to 239 ± 51 ml/min, P = 0.58). Oxygen extraction accordingly fell from 43 ± 10 to 30 ± 10% (P = 0.008). None of these changes occurred in either sham controls or pigs infused with lactic acid (final arterial pH 6.86 ± 0.16 and lactate 22 ± 3 mmol/L). Metformin intoxication was associated with inhibition of complex I in the liver (P < 0.001), heart (P < 0.001), kidney (P = 0.003), skeletal muscle (P = 0.012) and platelets (P = 0.053). The activity of complex II and III diminished in the liver (P < 0.001), heart (P < 0.001) and kidney (P < 0.005) while that of complex IV declined in the heart (P < 0.001). CONCLUSIONS: Metformin intoxication induces lactic acidosis, inhibits global oxygen consumption and causes mitochondrial dysfunction in liver and other tissues. Lactic acidosis per se does not decrease whole-body respiration. BioMed Central 2012 2012-05-08 /pmc/articles/PMC3580617/ /pubmed/22568883 http://dx.doi.org/10.1186/cc11332 Text en Copyright ©2012 Protti 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
Protti, Alessandro
Fortunato, Francesco
Monti, Massimo
Vecchio, Sarah
Gatti, Stefano
Comi, Giacomo P
De Giuseppe, Rachele
Gattinoni, Luciano
Metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs
title Metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs
title_full Metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs
title_fullStr Metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs
title_full_unstemmed Metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs
title_short Metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs
title_sort metformin overdose, but not lactic acidosis per se, inhibits oxygen consumption in pigs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580617/
https://www.ncbi.nlm.nih.gov/pubmed/22568883
http://dx.doi.org/10.1186/cc11332
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