Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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
_version_ 1785027614797201408
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
work_keys_str_mv AT zordaooliviapizetta maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT campolimclaramachado maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT yariwakevictoryuji maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT castrogisele maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT ferreiracliltonkraussdeoliveira maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT santosandrey maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT norbertosonia maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT verasmarianamatera maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT saadmariojoseabdalla maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT saldivapaulohilarionascimento maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT kimyoungbum maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota
AT pradapatriciaoliveira maternalexposuretoairpollutionaltersenergybalancetransientlyaccordingtogenderandchangesgutmicrobiota