Glucose fluctuation promotes mitochondrial dysfunctions in the cardiomyocyte cell line HL-1.

<h4>Aims</h4>Glycemic variability has been suggested as a risk factor for diabetes complications but the precise deleterious mechanisms remain poorly understood. Since mitochondria are the main source of energy in heart and cardiovascular diseases remain the first cause of death in patie...

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Main Authors: Patrick Mordel, Fanny Fontaine, Quentin Dupas, Michael Joubert, Stéphane Allouche
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0289475
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author Patrick Mordel
Fanny Fontaine
Quentin Dupas
Michael Joubert
Stéphane Allouche
author_facet Patrick Mordel
Fanny Fontaine
Quentin Dupas
Michael Joubert
Stéphane Allouche
author_sort Patrick Mordel
collection DOAJ
description <h4>Aims</h4>Glycemic variability has been suggested as a risk factor for diabetes complications but the precise deleterious mechanisms remain poorly understood. Since mitochondria are the main source of energy in heart and cardiovascular diseases remain the first cause of death in patients with diabetes, the aim of the study was to evaluate the impact of glucose swings on mitochondrial functions in the cardiomyocyte cell line HL-1.<h4>Methods</h4>HL-1 cells were exposed to low (LG, 2.8 mmol/l), normal (NG, 5.5 mmol/l), high (HG, 25 mmol/l) or intermittent high glucose (IHG, swing between low and high) every 2h during 12h (short-time treatment) or every 12h during 72h (long-time treatment). Anaerobic catabolism of glucose was evaluated by measuring glucose consumption and lactate production, oxidative phosphorylation was evaluated by polarography and ATP measurement, mitochondrial superoxide anions and the mitochondrial membrane potential (MMP) were analysed using fluorescent probes, and the protein oxidation was measured by oxyblot.<h4>Results</h4>IHG and HG increased glucose consumption and lactate production compared to LG and NG but without any difference between short- and long-time treatments. After 72h and unlike to LG, NG and HG, we didn't observe any increase of the mitochondrial respiration in the presence of succinate upon IHG treatment. IHG, and to a lesser extent HG, promoted a time-dependent decrease of the mitochondrial membrane potential compared to LG and NG treatments. HG and IHG also increased superoxide anion production compared to LG and NG both at 12 and 72h but with a higher increase for IHG at 72h. At last, both HG and IHG stimulated protein oxidation at 72h compared to LG and NG treatments.<h4>Conclusions</h4>Our results demonstrated that exposure of HL-1 cells to glucose swings promoted time-dependent mitochondrial dysfunctions suggesting a deleterious effect of such condition in patients with diabetes that could contribute to diabetic cardiomyopathy.
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spelling doaj.art-c2a36b18880643829b99b46b7605146f2023-09-28T05:31:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01189e028947510.1371/journal.pone.0289475Glucose fluctuation promotes mitochondrial dysfunctions in the cardiomyocyte cell line HL-1.Patrick MordelFanny FontaineQuentin DupasMichael JoubertStéphane Allouche<h4>Aims</h4>Glycemic variability has been suggested as a risk factor for diabetes complications but the precise deleterious mechanisms remain poorly understood. Since mitochondria are the main source of energy in heart and cardiovascular diseases remain the first cause of death in patients with diabetes, the aim of the study was to evaluate the impact of glucose swings on mitochondrial functions in the cardiomyocyte cell line HL-1.<h4>Methods</h4>HL-1 cells were exposed to low (LG, 2.8 mmol/l), normal (NG, 5.5 mmol/l), high (HG, 25 mmol/l) or intermittent high glucose (IHG, swing between low and high) every 2h during 12h (short-time treatment) or every 12h during 72h (long-time treatment). Anaerobic catabolism of glucose was evaluated by measuring glucose consumption and lactate production, oxidative phosphorylation was evaluated by polarography and ATP measurement, mitochondrial superoxide anions and the mitochondrial membrane potential (MMP) were analysed using fluorescent probes, and the protein oxidation was measured by oxyblot.<h4>Results</h4>IHG and HG increased glucose consumption and lactate production compared to LG and NG but without any difference between short- and long-time treatments. After 72h and unlike to LG, NG and HG, we didn't observe any increase of the mitochondrial respiration in the presence of succinate upon IHG treatment. IHG, and to a lesser extent HG, promoted a time-dependent decrease of the mitochondrial membrane potential compared to LG and NG treatments. HG and IHG also increased superoxide anion production compared to LG and NG both at 12 and 72h but with a higher increase for IHG at 72h. At last, both HG and IHG stimulated protein oxidation at 72h compared to LG and NG treatments.<h4>Conclusions</h4>Our results demonstrated that exposure of HL-1 cells to glucose swings promoted time-dependent mitochondrial dysfunctions suggesting a deleterious effect of such condition in patients with diabetes that could contribute to diabetic cardiomyopathy.https://doi.org/10.1371/journal.pone.0289475
spellingShingle Patrick Mordel
Fanny Fontaine
Quentin Dupas
Michael Joubert
Stéphane Allouche
Glucose fluctuation promotes mitochondrial dysfunctions in the cardiomyocyte cell line HL-1.
PLoS ONE
title Glucose fluctuation promotes mitochondrial dysfunctions in the cardiomyocyte cell line HL-1.
title_full Glucose fluctuation promotes mitochondrial dysfunctions in the cardiomyocyte cell line HL-1.
title_fullStr Glucose fluctuation promotes mitochondrial dysfunctions in the cardiomyocyte cell line HL-1.
title_full_unstemmed Glucose fluctuation promotes mitochondrial dysfunctions in the cardiomyocyte cell line HL-1.
title_short Glucose fluctuation promotes mitochondrial dysfunctions in the cardiomyocyte cell line HL-1.
title_sort glucose fluctuation promotes mitochondrial dysfunctions in the cardiomyocyte cell line hl 1
url https://doi.org/10.1371/journal.pone.0289475
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