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Methoxychlor exposure induces oxidative stress and affects mouse oocyte meiotic maturation
SUMMARY Methoxychlor (MXC) is used worldwide against insects and other pests. This organochlorine pesticide acts as a xenoestrogen, promotes oxidative stress, and is considered cytotoxic and genotoxic, causing abortions and stillbirths in females. Mechanistically related estrogens and oxidants affec...
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Published in: | Molecular reproduction and development 2016-09, Vol.83 (9), p.768-779 |
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container_title | Molecular reproduction and development |
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creator | Liu, Yu Wang, Ya-Long Chen, Ming-Huang Zhang, Zhen Xu, Bai-Hui Liu, Rui Xu, Lin He, Shu-Wen Li, Fei-Ping Qi, Zhong-Quan Wang, Hai-Long |
description | SUMMARY
Methoxychlor (MXC) is used worldwide against insects and other pests. This organochlorine pesticide acts as a xenoestrogen, promotes oxidative stress, and is considered cytotoxic and genotoxic, causing abortions and stillbirths in females. Mechanistically related estrogens and oxidants affect oocyte meiosis, so we investigated the effects of MXC on mouse oocyte meiotic maturation. Our results showed that maturation rates of MXC‐treated oocytes were lower than those of controls, which was due to abnormal spindle morphologies and DNA double‐strand breaks, as confirmed by increased γ‐H2AX foci. Our findings also suggest that MXC may affect oocyte quality by causing the accumulation of superoxide radicals and other reactive oxygen species, aberrant mitochondrial distribution, decreased mitochondrial membrane potential, and increased lipid peroxidation. Thus, exposure to MXC negatively affects oocyte meiotic maturation, primarily through impairments in cellular ROS metabolism. Mol. Reprod. Dev. 83: 768–779, 2016 © 2016 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/mrd.22683 |
format | article |
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Methoxychlor (MXC) is used worldwide against insects and other pests. This organochlorine pesticide acts as a xenoestrogen, promotes oxidative stress, and is considered cytotoxic and genotoxic, causing abortions and stillbirths in females. Mechanistically related estrogens and oxidants affect oocyte meiosis, so we investigated the effects of MXC on mouse oocyte meiotic maturation. Our results showed that maturation rates of MXC‐treated oocytes were lower than those of controls, which was due to abnormal spindle morphologies and DNA double‐strand breaks, as confirmed by increased γ‐H2AX foci. Our findings also suggest that MXC may affect oocyte quality by causing the accumulation of superoxide radicals and other reactive oxygen species, aberrant mitochondrial distribution, decreased mitochondrial membrane potential, and increased lipid peroxidation. Thus, exposure to MXC negatively affects oocyte meiotic maturation, primarily through impairments in cellular ROS metabolism. Mol. Reprod. Dev. 83: 768–779, 2016 © 2016 Wiley Periodicals, Inc.</description><identifier>ISSN: 1040-452X</identifier><identifier>EISSN: 1098-2795</identifier><identifier>DOI: 10.1002/mrd.22683</identifier><identifier>PMID: 27434785</identifier><identifier>CODEN: MREDEE</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animals ; DNA Breaks, Double-Stranded ; Female ; Meiosis - drug effects ; Membrane Potential, Mitochondrial - drug effects ; Methoxychlor - adverse effects ; Methoxychlor - pharmacology ; Mice ; Mice, Inbred ICR ; Oocytes - metabolism ; Oocytes - pathology ; Oxidative Stress - drug effects ; Superoxides - metabolism</subject><ispartof>Molecular reproduction and development, 2016-09, Vol.83 (9), p.768-779</ispartof><rights>2016 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4603-67804be1243629c754a4d76d94cf0726339178e86d685b72fdbdbfee2a1887483</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27434785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Yu</creatorcontrib><creatorcontrib>Wang, Ya-Long</creatorcontrib><creatorcontrib>Chen, Ming-Huang</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Xu, Bai-Hui</creatorcontrib><creatorcontrib>Liu, Rui</creatorcontrib><creatorcontrib>Xu, Lin</creatorcontrib><creatorcontrib>He, Shu-Wen</creatorcontrib><creatorcontrib>Li, Fei-Ping</creatorcontrib><creatorcontrib>Qi, Zhong-Quan</creatorcontrib><creatorcontrib>Wang, Hai-Long</creatorcontrib><title>Methoxychlor exposure induces oxidative stress and affects mouse oocyte meiotic maturation</title><title>Molecular reproduction and development</title><addtitle>Mol. Reprod. Dev</addtitle><description>SUMMARY
Methoxychlor (MXC) is used worldwide against insects and other pests. This organochlorine pesticide acts as a xenoestrogen, promotes oxidative stress, and is considered cytotoxic and genotoxic, causing abortions and stillbirths in females. Mechanistically related estrogens and oxidants affect oocyte meiosis, so we investigated the effects of MXC on mouse oocyte meiotic maturation. Our results showed that maturation rates of MXC‐treated oocytes were lower than those of controls, which was due to abnormal spindle morphologies and DNA double‐strand breaks, as confirmed by increased γ‐H2AX foci. Our findings also suggest that MXC may affect oocyte quality by causing the accumulation of superoxide radicals and other reactive oxygen species, aberrant mitochondrial distribution, decreased mitochondrial membrane potential, and increased lipid peroxidation. Thus, exposure to MXC negatively affects oocyte meiotic maturation, primarily through impairments in cellular ROS metabolism. Mol. Reprod. Dev. 83: 768–779, 2016 © 2016 Wiley Periodicals, Inc.</description><subject>Animals</subject><subject>DNA Breaks, Double-Stranded</subject><subject>Female</subject><subject>Meiosis - drug effects</subject><subject>Membrane Potential, Mitochondrial - drug effects</subject><subject>Methoxychlor - adverse effects</subject><subject>Methoxychlor - pharmacology</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Oocytes - metabolism</subject><subject>Oocytes - pathology</subject><subject>Oxidative Stress - drug effects</subject><subject>Superoxides - metabolism</subject><issn>1040-452X</issn><issn>1098-2795</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkU9v1DAQxS0EoqVw4AsgS1y4pPV_O0fUQkFqi0DAIi6WY09UlyRebAd2vz3ZbumBE6d50vzeaGYeQs8pOaaEsJMxh2PGlOEP0CElrWmYbuXDnRakEZJ9O0BPSrkhhLStIY_RAdOCC23kIfp-CfU6bbb-ekgZw2adypwBxynMHgpOmxhcjb8Al5qhFOymgF3fg68Fj2kugFPy2wp4hJhq9Hh0dc6LJU1P0aPeDQWe3dUj9OXtm8-n75qLD-fvT19fNF4owhulDREdUCa4Yq3XUjgRtAqt8D3RTHHeUm3AqKCM7DTrQxe6HoA5aowWhh-hV_u565x-zlCqHWPxMAxugmVDSw3XnGlp9H-gTGnWEs4X9OU_6E2a87QcsqO0UVJStVAv7qi5GyHYdY6jy1v798ELcLIHfscBtvd9SuwuObskZ2-Ts5efzm7F4mj2jlgqbO4dLv-wSnMt7erq3KrVx69XjK9sy_8AnpqZlg</recordid><startdate>201609</startdate><enddate>201609</enddate><creator>Liu, Yu</creator><creator>Wang, Ya-Long</creator><creator>Chen, Ming-Huang</creator><creator>Zhang, Zhen</creator><creator>Xu, Bai-Hui</creator><creator>Liu, Rui</creator><creator>Xu, Lin</creator><creator>He, Shu-Wen</creator><creator>Li, Fei-Ping</creator><creator>Qi, Zhong-Quan</creator><creator>Wang, Hai-Long</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QP</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201609</creationdate><title>Methoxychlor exposure induces oxidative stress and affects mouse oocyte meiotic maturation</title><author>Liu, Yu ; Wang, Ya-Long ; Chen, Ming-Huang ; Zhang, Zhen ; Xu, Bai-Hui ; Liu, Rui ; Xu, Lin ; He, Shu-Wen ; Li, Fei-Ping ; Qi, Zhong-Quan ; Wang, Hai-Long</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4603-67804be1243629c754a4d76d94cf0726339178e86d685b72fdbdbfee2a1887483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>DNA Breaks, Double-Stranded</topic><topic>Female</topic><topic>Meiosis - drug effects</topic><topic>Membrane Potential, Mitochondrial - drug effects</topic><topic>Methoxychlor - adverse effects</topic><topic>Methoxychlor - pharmacology</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Oocytes - metabolism</topic><topic>Oocytes - pathology</topic><topic>Oxidative Stress - drug effects</topic><topic>Superoxides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Yu</creatorcontrib><creatorcontrib>Wang, Ya-Long</creatorcontrib><creatorcontrib>Chen, Ming-Huang</creatorcontrib><creatorcontrib>Zhang, Zhen</creatorcontrib><creatorcontrib>Xu, Bai-Hui</creatorcontrib><creatorcontrib>Liu, Rui</creatorcontrib><creatorcontrib>Xu, Lin</creatorcontrib><creatorcontrib>He, Shu-Wen</creatorcontrib><creatorcontrib>Li, Fei-Ping</creatorcontrib><creatorcontrib>Qi, Zhong-Quan</creatorcontrib><creatorcontrib>Wang, Hai-Long</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular reproduction and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Yu</au><au>Wang, Ya-Long</au><au>Chen, Ming-Huang</au><au>Zhang, Zhen</au><au>Xu, Bai-Hui</au><au>Liu, Rui</au><au>Xu, Lin</au><au>He, Shu-Wen</au><au>Li, Fei-Ping</au><au>Qi, Zhong-Quan</au><au>Wang, Hai-Long</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methoxychlor exposure induces oxidative stress and affects mouse oocyte meiotic maturation</atitle><jtitle>Molecular reproduction and development</jtitle><addtitle>Mol. Reprod. Dev</addtitle><date>2016-09</date><risdate>2016</risdate><volume>83</volume><issue>9</issue><spage>768</spage><epage>779</epage><pages>768-779</pages><issn>1040-452X</issn><eissn>1098-2795</eissn><coden>MREDEE</coden><abstract>SUMMARY
Methoxychlor (MXC) is used worldwide against insects and other pests. This organochlorine pesticide acts as a xenoestrogen, promotes oxidative stress, and is considered cytotoxic and genotoxic, causing abortions and stillbirths in females. Mechanistically related estrogens and oxidants affect oocyte meiosis, so we investigated the effects of MXC on mouse oocyte meiotic maturation. Our results showed that maturation rates of MXC‐treated oocytes were lower than those of controls, which was due to abnormal spindle morphologies and DNA double‐strand breaks, as confirmed by increased γ‐H2AX foci. Our findings also suggest that MXC may affect oocyte quality by causing the accumulation of superoxide radicals and other reactive oxygen species, aberrant mitochondrial distribution, decreased mitochondrial membrane potential, and increased lipid peroxidation. Thus, exposure to MXC negatively affects oocyte meiotic maturation, primarily through impairments in cellular ROS metabolism. Mol. Reprod. Dev. 83: 768–779, 2016 © 2016 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>27434785</pmid><doi>10.1002/mrd.22683</doi><tpages>12</tpages></addata></record> |
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subjects | Animals DNA Breaks, Double-Stranded Female Meiosis - drug effects Membrane Potential, Mitochondrial - drug effects Methoxychlor - adverse effects Methoxychlor - pharmacology Mice Mice, Inbred ICR Oocytes - metabolism Oocytes - pathology Oxidative Stress - drug effects Superoxides - metabolism |
title | Methoxychlor exposure induces oxidative stress and affects mouse oocyte meiotic maturation |
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