Cargando…

Ovarian Damages Produced by Aerosolized Fine Particulate Matter (PM(2.5)) Pollution in Mice: Possible Protective Medications and Mechanisms

BACKGROUND: Ambient aerosol fine particulate matter (PM(2.5)) is associated with male reproductive toxicity in experiments and may have adverse effects in the female. However, studies evaluating the protective effects and precise mechanisms of aspirin, Vitamin C, Vitamin E, or ozone against toxic ef...

Descripción completa

Detalles Bibliográficos
Autores principales: Gai, Hui-Fang, An, Jian-Xiong, Qian, Xiao-Yan, Wei, Yong-Jie, Williams, John P, Gao, Guo-Lan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463468/
https://www.ncbi.nlm.nih.gov/pubmed/28584201
http://dx.doi.org/10.4103/0366-6999.207472
_version_ 1783242715150942208
author Gai, Hui-Fang
An, Jian-Xiong
Qian, Xiao-Yan
Wei, Yong-Jie
Williams, John P
Gao, Guo-Lan
author_facet Gai, Hui-Fang
An, Jian-Xiong
Qian, Xiao-Yan
Wei, Yong-Jie
Williams, John P
Gao, Guo-Lan
author_sort Gai, Hui-Fang
collection PubMed
description BACKGROUND: Ambient aerosol fine particulate matter (PM(2.5)) is associated with male reproductive toxicity in experiments and may have adverse effects in the female. However, studies evaluating the protective effects and precise mechanisms of aspirin, Vitamin C, Vitamin E, or ozone against toxic effects of PM(2.5) are sparse. This study was conducted to investigate the possible protective effects and mechanisms of aspirin, Vitamin C, Vitamin E, or ozone on fertility in female mice treated with PM(2.5). METHODS: Eighty-four ICR mice were divided into six groups: control group, PM(2.5) group, PM(2.5) + aspirin group, PM(2.5) + Vitamin C group, PM(2.5) + Vitamin E group, and PM(2.5) + ozone group. PM(2.5) was given by intratracheal instillation every 2 days for 3 weeks. Aspirin, Vitamin C, and Vitamin E were given once a day by oral gavage for 3 weeks, and ozone was administered by intraperitoneal injection once a day for 3 weeks. The levels of anti-Müllerian hormone (AMH), interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), and 8-hydroxy-2’-deoxyguanosine (8-OHdG) were measured using enzyme-linked immunosorbent assay. Western blotting analysis was used to analyze the expressions of Bcl-2, Bax, and caspase-3 in ovaries. Changes in histological structure were examined by light microscope and electron microscopy was used to detect ultramicrostructure. RESULTS: The results demonstrated that PM(2.5) decreased AMH levels (P < 0.001); however, aspirin (P < 0.001), Vitamin C (P < 0.001), Vitamin E (P = 0.001), and ozone (P = 0.002) alleviated the decrease. Changes of IL-6, TNF-α, 8-OHdG, Bax/Bcl-2, and caspase-3 in PM(2.5) group were increased compared to control group (P < 0.001), while in PM(2.5) + aspirin, PM(2.5) + Vitamin C, PM(2.5) + Vitamin E, and PM(2.5) + ozone groups, they were statistically decreased compared to PM(2.5) group (P < 0.001 or P < 0.05). CONCLUSIONS: PM(2.5) cause the damage of ovaries, and aspirin, Vitamin C, Vitamin E, and ozone antagonizes the damage. The protective mechanism is probably due to its ability to blunt the inflammatory and oxidative stress caused by PM(2.5), which subsequently suppressing the expression of apoptotic regulatory protein and reducing the incidence of ovary apoptosis.
format Online
Article
Text
id pubmed-5463468
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-54634682017-06-20 Ovarian Damages Produced by Aerosolized Fine Particulate Matter (PM(2.5)) Pollution in Mice: Possible Protective Medications and Mechanisms Gai, Hui-Fang An, Jian-Xiong Qian, Xiao-Yan Wei, Yong-Jie Williams, John P Gao, Guo-Lan Chin Med J (Engl) Original Article BACKGROUND: Ambient aerosol fine particulate matter (PM(2.5)) is associated with male reproductive toxicity in experiments and may have adverse effects in the female. However, studies evaluating the protective effects and precise mechanisms of aspirin, Vitamin C, Vitamin E, or ozone against toxic effects of PM(2.5) are sparse. This study was conducted to investigate the possible protective effects and mechanisms of aspirin, Vitamin C, Vitamin E, or ozone on fertility in female mice treated with PM(2.5). METHODS: Eighty-four ICR mice were divided into six groups: control group, PM(2.5) group, PM(2.5) + aspirin group, PM(2.5) + Vitamin C group, PM(2.5) + Vitamin E group, and PM(2.5) + ozone group. PM(2.5) was given by intratracheal instillation every 2 days for 3 weeks. Aspirin, Vitamin C, and Vitamin E were given once a day by oral gavage for 3 weeks, and ozone was administered by intraperitoneal injection once a day for 3 weeks. The levels of anti-Müllerian hormone (AMH), interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α), and 8-hydroxy-2’-deoxyguanosine (8-OHdG) were measured using enzyme-linked immunosorbent assay. Western blotting analysis was used to analyze the expressions of Bcl-2, Bax, and caspase-3 in ovaries. Changes in histological structure were examined by light microscope and electron microscopy was used to detect ultramicrostructure. RESULTS: The results demonstrated that PM(2.5) decreased AMH levels (P < 0.001); however, aspirin (P < 0.001), Vitamin C (P < 0.001), Vitamin E (P = 0.001), and ozone (P = 0.002) alleviated the decrease. Changes of IL-6, TNF-α, 8-OHdG, Bax/Bcl-2, and caspase-3 in PM(2.5) group were increased compared to control group (P < 0.001), while in PM(2.5) + aspirin, PM(2.5) + Vitamin C, PM(2.5) + Vitamin E, and PM(2.5) + ozone groups, they were statistically decreased compared to PM(2.5) group (P < 0.001 or P < 0.05). CONCLUSIONS: PM(2.5) cause the damage of ovaries, and aspirin, Vitamin C, Vitamin E, and ozone antagonizes the damage. The protective mechanism is probably due to its ability to blunt the inflammatory and oxidative stress caused by PM(2.5), which subsequently suppressing the expression of apoptotic regulatory protein and reducing the incidence of ovary apoptosis. Medknow Publications & Media Pvt Ltd 2017-06-20 /pmc/articles/PMC5463468/ /pubmed/28584201 http://dx.doi.org/10.4103/0366-6999.207472 Text en Copyright: © 2017 Chinese Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Gai, Hui-Fang
An, Jian-Xiong
Qian, Xiao-Yan
Wei, Yong-Jie
Williams, John P
Gao, Guo-Lan
Ovarian Damages Produced by Aerosolized Fine Particulate Matter (PM(2.5)) Pollution in Mice: Possible Protective Medications and Mechanisms
title Ovarian Damages Produced by Aerosolized Fine Particulate Matter (PM(2.5)) Pollution in Mice: Possible Protective Medications and Mechanisms
title_full Ovarian Damages Produced by Aerosolized Fine Particulate Matter (PM(2.5)) Pollution in Mice: Possible Protective Medications and Mechanisms
title_fullStr Ovarian Damages Produced by Aerosolized Fine Particulate Matter (PM(2.5)) Pollution in Mice: Possible Protective Medications and Mechanisms
title_full_unstemmed Ovarian Damages Produced by Aerosolized Fine Particulate Matter (PM(2.5)) Pollution in Mice: Possible Protective Medications and Mechanisms
title_short Ovarian Damages Produced by Aerosolized Fine Particulate Matter (PM(2.5)) Pollution in Mice: Possible Protective Medications and Mechanisms
title_sort ovarian damages produced by aerosolized fine particulate matter (pm(2.5)) pollution in mice: possible protective medications and mechanisms
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463468/
https://www.ncbi.nlm.nih.gov/pubmed/28584201
http://dx.doi.org/10.4103/0366-6999.207472
work_keys_str_mv AT gaihuifang ovariandamagesproducedbyaerosolizedfineparticulatematterpm25pollutioninmicepossibleprotectivemedicationsandmechanisms
AT anjianxiong ovariandamagesproducedbyaerosolizedfineparticulatematterpm25pollutioninmicepossibleprotectivemedicationsandmechanisms
AT qianxiaoyan ovariandamagesproducedbyaerosolizedfineparticulatematterpm25pollutioninmicepossibleprotectivemedicationsandmechanisms
AT weiyongjie ovariandamagesproducedbyaerosolizedfineparticulatematterpm25pollutioninmicepossibleprotectivemedicationsandmechanisms
AT williamsjohnp ovariandamagesproducedbyaerosolizedfineparticulatematterpm25pollutioninmicepossibleprotectivemedicationsandmechanisms
AT gaoguolan ovariandamagesproducedbyaerosolizedfineparticulatematterpm25pollutioninmicepossibleprotectivemedicationsandmechanisms