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Sex-Dependent Responses to Maternal Exposure to PM(2.5) in the Offspring
Objective: Particulate matter (PM) with a diameter of 2.5 μm or less (PM(2.5)) can cross the blood-placental barrier causing adverse foetal outcomes. However, the impact of maternal exposure to low-levels of PM(2.5) on liver health and the metabolic profile is unclear. This study aimed to investigat...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686974/ https://www.ncbi.nlm.nih.gov/pubmed/36421441 http://dx.doi.org/10.3390/antiox11112255 |
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author | Chen, Hui Van Reyk, David Oliveira, Annabel Chan, Yik Lung Town, Stephanie EL Rayner, Benjamin Pollock, Carol A Saad, Sonia George, Jacob Padula, Matthew P Oliver, Brian G |
author_facet | Chen, Hui Van Reyk, David Oliveira, Annabel Chan, Yik Lung Town, Stephanie EL Rayner, Benjamin Pollock, Carol A Saad, Sonia George, Jacob Padula, Matthew P Oliver, Brian G |
author_sort | Chen, Hui |
collection | PubMed |
description | Objective: Particulate matter (PM) with a diameter of 2.5 μm or less (PM(2.5)) can cross the blood-placental barrier causing adverse foetal outcomes. However, the impact of maternal exposure to low-levels of PM(2.5) on liver health and the metabolic profile is unclear. This study aimed to investigate hepatic responses to long-term gestational low-dose PM(2.5) exposure, and whether the removal of PM after conception can prevent such effects. Method: Female Balb/c mice (8 weeks) were exposed to PM(2.5) (5 μg/day) for 6 weeks prior to mating, during gestation and lactation to model living in a polluted environment (PM group). In a sub-group, PM(2.5) exposure was stopped post-conception to model mothers moving to areas with clean air (pre-gestation, Pre) group. Livers were studied in 13-week old offspring. Results: Female offspring in both PM and Pre groups had increased liver triglyceride and glycogen levels, glucose intolerance, but reduced serum insulin and insulin resistance. Male offspring from only the Pre group had increased liver and serum triglycerides, increased liver glycogen, glucose intolerance and higher fasting glucose level. Markers of oxidative stress and inflammation were increased in females from PM and Pre groups. There was also a significant sex difference in the hepatic response to PM(2.5) with differential changes in several metabolic markers identified by proteomic analysis. Conclusions: Maternal PM exposure exerted sex-dependent effects on liver health with more severe impacts on females. The removal of PM(2.5) during gestation provided limited protection in the offspring’s metabolism regardless of sex. |
format | Online Article Text |
id | pubmed-9686974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96869742022-11-25 Sex-Dependent Responses to Maternal Exposure to PM(2.5) in the Offspring Chen, Hui Van Reyk, David Oliveira, Annabel Chan, Yik Lung Town, Stephanie EL Rayner, Benjamin Pollock, Carol A Saad, Sonia George, Jacob Padula, Matthew P Oliver, Brian G Antioxidants (Basel) Article Objective: Particulate matter (PM) with a diameter of 2.5 μm or less (PM(2.5)) can cross the blood-placental barrier causing adverse foetal outcomes. However, the impact of maternal exposure to low-levels of PM(2.5) on liver health and the metabolic profile is unclear. This study aimed to investigate hepatic responses to long-term gestational low-dose PM(2.5) exposure, and whether the removal of PM after conception can prevent such effects. Method: Female Balb/c mice (8 weeks) were exposed to PM(2.5) (5 μg/day) for 6 weeks prior to mating, during gestation and lactation to model living in a polluted environment (PM group). In a sub-group, PM(2.5) exposure was stopped post-conception to model mothers moving to areas with clean air (pre-gestation, Pre) group. Livers were studied in 13-week old offspring. Results: Female offspring in both PM and Pre groups had increased liver triglyceride and glycogen levels, glucose intolerance, but reduced serum insulin and insulin resistance. Male offspring from only the Pre group had increased liver and serum triglycerides, increased liver glycogen, glucose intolerance and higher fasting glucose level. Markers of oxidative stress and inflammation were increased in females from PM and Pre groups. There was also a significant sex difference in the hepatic response to PM(2.5) with differential changes in several metabolic markers identified by proteomic analysis. Conclusions: Maternal PM exposure exerted sex-dependent effects on liver health with more severe impacts on females. The removal of PM(2.5) during gestation provided limited protection in the offspring’s metabolism regardless of sex. MDPI 2022-11-15 /pmc/articles/PMC9686974/ /pubmed/36421441 http://dx.doi.org/10.3390/antiox11112255 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chen, Hui Van Reyk, David Oliveira, Annabel Chan, Yik Lung Town, Stephanie EL Rayner, Benjamin Pollock, Carol A Saad, Sonia George, Jacob Padula, Matthew P Oliver, Brian G Sex-Dependent Responses to Maternal Exposure to PM(2.5) in the Offspring |
title | Sex-Dependent Responses to Maternal Exposure to PM(2.5) in the Offspring |
title_full | Sex-Dependent Responses to Maternal Exposure to PM(2.5) in the Offspring |
title_fullStr | Sex-Dependent Responses to Maternal Exposure to PM(2.5) in the Offspring |
title_full_unstemmed | Sex-Dependent Responses to Maternal Exposure to PM(2.5) in the Offspring |
title_short | Sex-Dependent Responses to Maternal Exposure to PM(2.5) in the Offspring |
title_sort | sex-dependent responses to maternal exposure to pm(2.5) in the offspring |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686974/ https://www.ncbi.nlm.nih.gov/pubmed/36421441 http://dx.doi.org/10.3390/antiox11112255 |
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