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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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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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. |
format | Online Article Text |
id | pubmed-10293596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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