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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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