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Subchronic exposure to 1,2-naphthoquinone induces adipose tissue inflammation and changes the energy homeostasis of mice, partially due to TNFR1 and TLR4

Air pollution affects energy homeostasis detrimentally. Yet, knowledge of how each isolated pollutant can impact energy metabolism remains incomplete. The present study was designed to investigate the distinct effects of 1,2-naphthoquinone (1,2-NQ) on energy metabolism since this pollutant increases...

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Autores principales: Oliveira Ferreira, Clílton Kraüss de, Campolim, Clara Machado, Zordão, Olívia Pizetta, Simabuco, Fernando Moreira, Anaruma, Chadi Pellegrini, Pereira, Rodrigo Martins, Boico, Vitor Ferreira, Salvino, Luiz Guilherme, Costa, Maíra Maftoum, Ruiz, Nathalia Quintero, de Moura, Leandro Pereira, Saad, Mario Jose Abdalla, Costa, Soraia Katia Pereira, Kim, Young-Bum, Prada, Patricia Oliveira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293596/
https://www.ncbi.nlm.nih.gov/pubmed/37383489
http://dx.doi.org/10.1016/j.toxrep.2023.06.002
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author Oliveira Ferreira, Clílton Kraüss de
Campolim, Clara Machado
Zordão, Olívia Pizetta
Simabuco, Fernando Moreira
Anaruma, Chadi Pellegrini
Pereira, Rodrigo Martins
Boico, Vitor Ferreira
Salvino, Luiz Guilherme
Costa, Maíra Maftoum
Ruiz, Nathalia Quintero
de Moura, Leandro Pereira
Saad, Mario Jose Abdalla
Costa, Soraia Katia Pereira
Kim, Young-Bum
Prada, Patricia Oliveira
author_facet Oliveira Ferreira, Clílton Kraüss de
Campolim, Clara Machado
Zordão, Olívia Pizetta
Simabuco, Fernando Moreira
Anaruma, Chadi Pellegrini
Pereira, Rodrigo Martins
Boico, Vitor Ferreira
Salvino, Luiz Guilherme
Costa, Maíra Maftoum
Ruiz, Nathalia Quintero
de Moura, Leandro Pereira
Saad, Mario Jose Abdalla
Costa, Soraia Katia Pereira
Kim, Young-Bum
Prada, Patricia Oliveira
author_sort Oliveira Ferreira, Clílton Kraüss de
collection PubMed
description Air pollution affects energy homeostasis detrimentally. Yet, knowledge of how each isolated pollutant can impact energy metabolism remains incomplete. The present study was designed to investigate the distinct effects of 1,2-naphthoquinone (1,2-NQ) on energy metabolism since this pollutant increases at the same rate as diesel combustion. In particular, we aimed to determine in vivo effects of subchronic exposure to 1,2-NQ on metabolic and inflammatory parameters of wild-type mice (WT) and to explore the involvement of tumor necrosis factor receptor 1 (TNFR1) and toll-like receptor 4 (TLR4) in this process. Males WT, TNFR1KO, and TLR4KO mice at eight weeks of age received 1,2-NQ or vehicle via nebulization five days a week for 17 weeks. In WT mice, 1,2-NQ slightly decreased the body mass compared to vehicle-WT. This effect was likely due to a mild food intake reduction and increased energy expenditure (EE) observed after six weeks of exposure. After nine weeks of exposure, we observed higher fasting blood glucose and impaired glucose tolerance, whereas insulin sensitivity was slightly improved compared to vehicle-WT. After 17 weeks of 1,2-NQ exposure, WT mice displayed an increased percentage of M1 and a decreased (p = 0.057) percentage of M2 macrophages in adipose tissue. The deletion of TNFR1 and TLR4 abolished most of the metabolic impacts caused by 1,2-NQ exposure, except for the EE and insulin sensitivity, which remained high in these mice under 1,2-NQ exposure. Our study demonstrates for the first time that subchronic exposure to 1,2-NQ affects energy metabolism in vivo. Although 1,2-NQ increased EE and slightly reduced feeding and body mass, the WT mice displayed higher inflammation in adipose tissue and impaired fasting blood glucose and glucose tolerance. Thus, in vivo subchronic exposure to 1,2-NQ is harmful, and TNFR1 and TLR4 are partially involved in these outcomes.
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spelling pubmed-102935962023-06-28 Subchronic exposure to 1,2-naphthoquinone induces adipose tissue inflammation and changes the energy homeostasis of mice, partially due to TNFR1 and TLR4 Oliveira Ferreira, Clílton Kraüss de Campolim, Clara Machado Zordão, Olívia Pizetta Simabuco, Fernando Moreira Anaruma, Chadi Pellegrini Pereira, Rodrigo Martins Boico, Vitor Ferreira Salvino, Luiz Guilherme Costa, Maíra Maftoum Ruiz, Nathalia Quintero de Moura, Leandro Pereira Saad, Mario Jose Abdalla Costa, Soraia Katia Pereira Kim, Young-Bum Prada, Patricia Oliveira Toxicol Rep Article Air pollution affects energy homeostasis detrimentally. Yet, knowledge of how each isolated pollutant can impact energy metabolism remains incomplete. The present study was designed to investigate the distinct effects of 1,2-naphthoquinone (1,2-NQ) on energy metabolism since this pollutant increases at the same rate as diesel combustion. In particular, we aimed to determine in vivo effects of subchronic exposure to 1,2-NQ on metabolic and inflammatory parameters of wild-type mice (WT) and to explore the involvement of tumor necrosis factor receptor 1 (TNFR1) and toll-like receptor 4 (TLR4) in this process. Males WT, TNFR1KO, and TLR4KO mice at eight weeks of age received 1,2-NQ or vehicle via nebulization five days a week for 17 weeks. In WT mice, 1,2-NQ slightly decreased the body mass compared to vehicle-WT. This effect was likely due to a mild food intake reduction and increased energy expenditure (EE) observed after six weeks of exposure. After nine weeks of exposure, we observed higher fasting blood glucose and impaired glucose tolerance, whereas insulin sensitivity was slightly improved compared to vehicle-WT. After 17 weeks of 1,2-NQ exposure, WT mice displayed an increased percentage of M1 and a decreased (p = 0.057) percentage of M2 macrophages in adipose tissue. The deletion of TNFR1 and TLR4 abolished most of the metabolic impacts caused by 1,2-NQ exposure, except for the EE and insulin sensitivity, which remained high in these mice under 1,2-NQ exposure. Our study demonstrates for the first time that subchronic exposure to 1,2-NQ affects energy metabolism in vivo. Although 1,2-NQ increased EE and slightly reduced feeding and body mass, the WT mice displayed higher inflammation in adipose tissue and impaired fasting blood glucose and glucose tolerance. Thus, in vivo subchronic exposure to 1,2-NQ is harmful, and TNFR1 and TLR4 are partially involved in these outcomes. Elsevier 2023-06-15 /pmc/articles/PMC10293596/ /pubmed/37383489 http://dx.doi.org/10.1016/j.toxrep.2023.06.002 Text en © 2023 The Authors. Published by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Oliveira Ferreira, Clílton Kraüss de
Campolim, Clara Machado
Zordão, Olívia Pizetta
Simabuco, Fernando Moreira
Anaruma, Chadi Pellegrini
Pereira, Rodrigo Martins
Boico, Vitor Ferreira
Salvino, Luiz Guilherme
Costa, Maíra Maftoum
Ruiz, Nathalia Quintero
de Moura, Leandro Pereira
Saad, Mario Jose Abdalla
Costa, Soraia Katia Pereira
Kim, Young-Bum
Prada, Patricia Oliveira
Subchronic exposure to 1,2-naphthoquinone induces adipose tissue inflammation and changes the energy homeostasis of mice, partially due to TNFR1 and TLR4
title Subchronic exposure to 1,2-naphthoquinone induces adipose tissue inflammation and changes the energy homeostasis of mice, partially due to TNFR1 and TLR4
title_full Subchronic exposure to 1,2-naphthoquinone induces adipose tissue inflammation and changes the energy homeostasis of mice, partially due to TNFR1 and TLR4
title_fullStr Subchronic exposure to 1,2-naphthoquinone induces adipose tissue inflammation and changes the energy homeostasis of mice, partially due to TNFR1 and TLR4
title_full_unstemmed Subchronic exposure to 1,2-naphthoquinone induces adipose tissue inflammation and changes the energy homeostasis of mice, partially due to TNFR1 and TLR4
title_short Subchronic exposure to 1,2-naphthoquinone induces adipose tissue inflammation and changes the energy homeostasis of mice, partially due to TNFR1 and TLR4
title_sort subchronic exposure to 1,2-naphthoquinone induces adipose tissue inflammation and changes the energy homeostasis of mice, partially due to tnfr1 and tlr4
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10293596/
https://www.ncbi.nlm.nih.gov/pubmed/37383489
http://dx.doi.org/10.1016/j.toxrep.2023.06.002
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