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Maternal exposure to air pollution alters energy balance transiently according to gender and changes gut microbiota
INTRODUCTION: The timing of maternal exposure to air pollution is crucial to define metabolic changes in the offspring. Here we aimed to determine the most critical period of maternal exposure to particulate matter (PM(2.5)) that impairs offspring's energy metabolism and gut microbiota composit...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10112381/ https://www.ncbi.nlm.nih.gov/pubmed/37082122 http://dx.doi.org/10.3389/fendo.2023.1069243 |
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author | Zordão, Olivia Pizetta Campolim, Clara Machado Yariwake, Victor Yuji Castro, Gisele Ferreira, Clílton Kraüss de Oliveira Santos, Andrey Norberto, Sónia Veras, Mariana Matera Saad, Mario Jose Abdalla Saldiva, Paulo Hilário Nascimento Kim, Young-Bum Prada, Patricia Oliveira |
author_facet | Zordão, Olivia Pizetta Campolim, Clara Machado Yariwake, Victor Yuji Castro, Gisele Ferreira, Clílton Kraüss de Oliveira Santos, Andrey Norberto, Sónia Veras, Mariana Matera Saad, Mario Jose Abdalla Saldiva, Paulo Hilário Nascimento Kim, Young-Bum Prada, Patricia Oliveira |
author_sort | Zordão, Olivia Pizetta |
collection | PubMed |
description | INTRODUCTION: The timing of maternal exposure to air pollution is crucial to define metabolic changes in the offspring. Here we aimed to determine the most critical period of maternal exposure to particulate matter (PM(2.5)) that impairs offspring's energy metabolism and gut microbiota composition. METHODS: Unexposed female and male C57BL/6J mice were mated. PM(2.5) or filtered air (FA) exposure occurred only in gestation (PM(2.5)/FA) or lactation (FA/PM(2.5)). We studied the offspring of both genders. RESULTS: PM(2.5) exposure during gestation increased body weight (BW) at birth and from weaning to young in male adulthood. Leptin levels, food intake, Agrp, and Npy levels in the hypothalamus were also increased in young male offspring. Ikbke, Tnf increased in male PM(2.5)/FA. Males from FA/PM(2.5) group were protected from these phenotypes showing higher O(2) consumption and Ucp1 in the brown adipose tissue. In female offspring, we did not see changes in BW at weaning. However, adult females from PM(2.5)/FA displayed higher BW and leptin levels, despite increased energy expenditure and thermogenesis. This group showed a slight increase in food intake. In female offspring from FA/PM(2.5), BW, and leptin levels were elevated. This group displayed higher energy expenditure and a mild increase in food intake. To determine if maternal exposure to PM(2.5) could affect the offspring’s gut microbiota, we analyzed alpha diversity by Shannon and Simpson indexes and beta diversity by the Linear Discriminant Analysis (LDA) in offspring at 30 weeks. Unlike males, exposure during gestation led to higher adiposity and leptin maintenance in female offspring at this age. Gestation exposure was associated with decreased alpha diversity in the gut microbiota in both genders. DISCUSSION: Our data support that exposure to air pollution during gestation is more harmful to metabolism than exposure during lactation. Male offspring had an unfavorable metabolic phenotype at a young age. However, at an older age, only females kept more adiposity. Ultimately, our data highlight the importance of controlling air pollution, especially during gestation. |
format | Online Article Text |
id | pubmed-10112381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101123812023-04-19 Maternal exposure to air pollution alters energy balance transiently according to gender and changes gut microbiota Zordão, Olivia Pizetta Campolim, Clara Machado Yariwake, Victor Yuji Castro, Gisele Ferreira, Clílton Kraüss de Oliveira Santos, Andrey Norberto, Sónia Veras, Mariana Matera Saad, Mario Jose Abdalla Saldiva, Paulo Hilário Nascimento Kim, Young-Bum Prada, Patricia Oliveira Front Endocrinol (Lausanne) Endocrinology INTRODUCTION: The timing of maternal exposure to air pollution is crucial to define metabolic changes in the offspring. Here we aimed to determine the most critical period of maternal exposure to particulate matter (PM(2.5)) that impairs offspring's energy metabolism and gut microbiota composition. METHODS: Unexposed female and male C57BL/6J mice were mated. PM(2.5) or filtered air (FA) exposure occurred only in gestation (PM(2.5)/FA) or lactation (FA/PM(2.5)). We studied the offspring of both genders. RESULTS: PM(2.5) exposure during gestation increased body weight (BW) at birth and from weaning to young in male adulthood. Leptin levels, food intake, Agrp, and Npy levels in the hypothalamus were also increased in young male offspring. Ikbke, Tnf increased in male PM(2.5)/FA. Males from FA/PM(2.5) group were protected from these phenotypes showing higher O(2) consumption and Ucp1 in the brown adipose tissue. In female offspring, we did not see changes in BW at weaning. However, adult females from PM(2.5)/FA displayed higher BW and leptin levels, despite increased energy expenditure and thermogenesis. This group showed a slight increase in food intake. In female offspring from FA/PM(2.5), BW, and leptin levels were elevated. This group displayed higher energy expenditure and a mild increase in food intake. To determine if maternal exposure to PM(2.5) could affect the offspring’s gut microbiota, we analyzed alpha diversity by Shannon and Simpson indexes and beta diversity by the Linear Discriminant Analysis (LDA) in offspring at 30 weeks. Unlike males, exposure during gestation led to higher adiposity and leptin maintenance in female offspring at this age. Gestation exposure was associated with decreased alpha diversity in the gut microbiota in both genders. DISCUSSION: Our data support that exposure to air pollution during gestation is more harmful to metabolism than exposure during lactation. Male offspring had an unfavorable metabolic phenotype at a young age. However, at an older age, only females kept more adiposity. Ultimately, our data highlight the importance of controlling air pollution, especially during gestation. Frontiers Media S.A. 2023-04-04 /pmc/articles/PMC10112381/ /pubmed/37082122 http://dx.doi.org/10.3389/fendo.2023.1069243 Text en Copyright © 2023 Zordão, Campolim, Yariwake, Castro, Ferreira, Santos, Norberto, Veras, Saad, Saldiva, Kim and Prada https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Zordão, Olivia Pizetta Campolim, Clara Machado Yariwake, Victor Yuji Castro, Gisele Ferreira, Clílton Kraüss de Oliveira Santos, Andrey Norberto, Sónia Veras, Mariana Matera Saad, Mario Jose Abdalla Saldiva, Paulo Hilário Nascimento Kim, Young-Bum Prada, Patricia Oliveira Maternal exposure to air pollution alters energy balance transiently according to gender and changes gut microbiota |
title | Maternal exposure to air pollution alters energy balance transiently according to gender and changes gut microbiota |
title_full | Maternal exposure to air pollution alters energy balance transiently according to gender and changes gut microbiota |
title_fullStr | Maternal exposure to air pollution alters energy balance transiently according to gender and changes gut microbiota |
title_full_unstemmed | Maternal exposure to air pollution alters energy balance transiently according to gender and changes gut microbiota |
title_short | Maternal exposure to air pollution alters energy balance transiently according to gender and changes gut microbiota |
title_sort | maternal exposure to air pollution alters energy balance transiently according to gender and changes gut microbiota |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10112381/ https://www.ncbi.nlm.nih.gov/pubmed/37082122 http://dx.doi.org/10.3389/fendo.2023.1069243 |
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