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High concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro

BACKGROUND: Dogs are commonly affected by hyperglycemic conditions. Hyperglycemia compromises the immune response and favors bacterial infections; however, reports on the effects of glucose on neutrophil oxidative metabolism and apoptosis are conflicting in humans and rare in dogs. Considering the m...

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Autores principales: Bosco, Anelise M, de Almeida, Breno FM, Pereira, Priscila P, Narciso, Luis G, Lima, Valéria MF, Ciarlini, Paulo C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568711/
https://www.ncbi.nlm.nih.gov/pubmed/23388121
http://dx.doi.org/10.1186/1746-6148-9-24
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author Bosco, Anelise M
de Almeida, Breno FM
Pereira, Priscila P
Narciso, Luis G
Lima, Valéria MF
Ciarlini, Paulo C
author_facet Bosco, Anelise M
de Almeida, Breno FM
Pereira, Priscila P
Narciso, Luis G
Lima, Valéria MF
Ciarlini, Paulo C
author_sort Bosco, Anelise M
collection PubMed
description BACKGROUND: Dogs are commonly affected by hyperglycemic conditions. Hyperglycemia compromises the immune response and favors bacterial infections; however, reports on the effects of glucose on neutrophil oxidative metabolism and apoptosis are conflicting in humans and rare in dogs. Considering the many complex factors that affect neutrophil oxidative metabolism in vivo, we investigated in vitro the specific effect of high concentrations of glucose on superoxide production and apoptosis rate in neutrophils from healthy dogs. RESULTS: The capacity of the neutrophils to reduce tetrazolium nitroblue decreased significantly in the higher concentration of glucose (15.13 ± 9.73% (8 mmol/L) versus 8.93 ± 5.71% (16 mmol/L)). However, there were no changes in tetrazolium nitroblue reduction at different glucose concentrations when the neutrophils were first activated with phorbol myristate acetate. High concentrations of glucose did not affect the viability and apoptosis rate of canine neutrophils either with or without prior camptothecin stimulation. This study provides the first evidence that high concentrations of glucose inhibit the oxidative metabolism of canine neutrophils in vitro in a manner similar to that which occurs in humans, and that the decrease in superoxide production did not increase the apoptosis rate. CONCLUSIONS: A high concentration of glucose reduces the oxidative metabolism of canine neutrophils in vitro. It is likely that glucose at high concentrations rapidly affects membrane receptors responsible for the activation of NADPH oxidase in neutrophils; therefore, the nonspecific immune response can be compromised in dogs with acute and chronic hyperglycemic conditions.
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spelling pubmed-35687112013-02-12 High concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro Bosco, Anelise M de Almeida, Breno FM Pereira, Priscila P Narciso, Luis G Lima, Valéria MF Ciarlini, Paulo C BMC Vet Res Research Article BACKGROUND: Dogs are commonly affected by hyperglycemic conditions. Hyperglycemia compromises the immune response and favors bacterial infections; however, reports on the effects of glucose on neutrophil oxidative metabolism and apoptosis are conflicting in humans and rare in dogs. Considering the many complex factors that affect neutrophil oxidative metabolism in vivo, we investigated in vitro the specific effect of high concentrations of glucose on superoxide production and apoptosis rate in neutrophils from healthy dogs. RESULTS: The capacity of the neutrophils to reduce tetrazolium nitroblue decreased significantly in the higher concentration of glucose (15.13 ± 9.73% (8 mmol/L) versus 8.93 ± 5.71% (16 mmol/L)). However, there were no changes in tetrazolium nitroblue reduction at different glucose concentrations when the neutrophils were first activated with phorbol myristate acetate. High concentrations of glucose did not affect the viability and apoptosis rate of canine neutrophils either with or without prior camptothecin stimulation. This study provides the first evidence that high concentrations of glucose inhibit the oxidative metabolism of canine neutrophils in vitro in a manner similar to that which occurs in humans, and that the decrease in superoxide production did not increase the apoptosis rate. CONCLUSIONS: A high concentration of glucose reduces the oxidative metabolism of canine neutrophils in vitro. It is likely that glucose at high concentrations rapidly affects membrane receptors responsible for the activation of NADPH oxidase in neutrophils; therefore, the nonspecific immune response can be compromised in dogs with acute and chronic hyperglycemic conditions. BioMed Central 2013-02-06 /pmc/articles/PMC3568711/ /pubmed/23388121 http://dx.doi.org/10.1186/1746-6148-9-24 Text en Copyright ©2013 Bosco 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 Article
Bosco, Anelise M
de Almeida, Breno FM
Pereira, Priscila P
Narciso, Luis G
Lima, Valéria MF
Ciarlini, Paulo C
High concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro
title High concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro
title_full High concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro
title_fullStr High concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro
title_full_unstemmed High concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro
title_short High concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro
title_sort high concentrations of glucose reduce the oxidative metabolism of dog neutrophils in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3568711/
https://www.ncbi.nlm.nih.gov/pubmed/23388121
http://dx.doi.org/10.1186/1746-6148-9-24
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