Cuproptosis is involved in decabromodiphenyl ether-induced ovarian dysfunction and the protective effect of melatonin
Decabromodiphenyl ether (BDE-209) has been universally detected in environmental media and animals, but its damage to ovarian function and mechanism is still unclear, and melatonin has been shown to improve mammalian ovarian function. This study aimed to investigate the toxic effects of BDE-209 on t...
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Veröffentlicht in: | Environmental pollution (1987) 2024-07, Vol.352, p.124100-124100, Article 124100 |
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description | Decabromodiphenyl ether (BDE-209) has been universally detected in environmental media and animals, but its damage to ovarian function and mechanism is still unclear, and melatonin has been shown to improve mammalian ovarian function. This study aimed to investigate the toxic effects of BDE-209 on the ovary and tried to improve ovarian function with melatonin. Herein, BDE-209 was administered orally to female SD rats for 60 days. Enzyme-linked immunosorbent assay, HE staining, transcriptome analysis, qPCR and immunohistochemical staining were used to explore and verify the potential mechanism. We found that BDE-209 exposure had effects on the ovary, as shown by abnormal changes in the estrous cycle, hormone levels and ovarian reserve function in rats, while increasing the proportion of collagen fibres in ovarian tissue. In terms of mechanism, cuproptosis, a form of cell death, was identified to play a crucial role in BDE-209-induced ovarian dysfunction, with the phenotype manifested as copper salt accumulation in ovary, downregulation of glutathione pathway metabolism and copper transfer molecule (ATP7A/B), and upregulation of FDX1, lipoic acid pathway (LIAS, LIPT1), pyruvate dehydrogenase complex components (DLAT, PDHB, PDHA1), and copper transfer molecule (SLC31A1). Furthermore, possible interventions were explored. Notably, a supplement with melatonin has a repair effect on the damage to ovarian function by reversing the gene expression of cuproptosis-involved molecules. Overall, this study revealed that cuproptosis is involved in BDE-209-induced ovarian damage and the beneficial effect of melatonin on ovarian copper damage, providing evidence for the prevention and control of female reproductive damage induced by BDE-209.
[Display omitted]
•Chronic exposure to BDE-209 leads to abnormal ovarian function.•Cuproptosis plays an important role in BDE-209-induced ovarian dysfunction.•Melatonin can change the expression of cuproptosis-related molecules.•Melatonin can improve the ovarian damage caused by BDE-209. |
doi_str_mv | 10.1016/j.envpol.2024.124100 |
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[Display omitted]
•Chronic exposure to BDE-209 leads to abnormal ovarian function.•Cuproptosis plays an important role in BDE-209-induced ovarian dysfunction.•Melatonin can change the expression of cuproptosis-related molecules.•Melatonin can improve the ovarian damage caused by BDE-209.</description><identifier>ISSN: 0269-7491</identifier><identifier>EISSN: 1873-6424</identifier><identifier>DOI: 10.1016/j.envpol.2024.124100</identifier><identifier>PMID: 38714232</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>cell death ; collagen ; Copper ; Cuproptosis ; decabromodiphenyl ether ; Endocrine disrupting chemicals ; enzyme-linked immunosorbent assay ; estrous cycle ; females ; gene expression ; glutathione ; immunohistochemistry ; lipoic acid ; mammals ; Melatonin ; metabolism ; Ovarian dysfunction ; phenotype ; pollution ; protective effect ; pyruvate dehydrogenase (lipoamide) ; toxicity ; transcriptomics</subject><ispartof>Environmental pollution (1987), 2024-07, Vol.352, p.124100-124100, Article 124100</ispartof><rights>2024 Elsevier Ltd</rights><rights>Copyright © 2024. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c344t-e1abc1ce3b38be94de84adee192540ab4a8da1fbc21b8025bfd2ddaf632d56eb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.envpol.2024.124100$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38714232$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Ziyan</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Huang, Danyang</creatorcontrib><creatorcontrib>Kang, Huiwen</creatorcontrib><creatorcontrib>Wang, Jingyu</creatorcontrib><creatorcontrib>Liu, Ziyan</creatorcontrib><creatorcontrib>Jiang, Guangyu</creatorcontrib><creatorcontrib>Gao, Ai</creatorcontrib><title>Cuproptosis is involved in decabromodiphenyl ether-induced ovarian dysfunction and the protective effect of melatonin</title><title>Environmental pollution (1987)</title><addtitle>Environ Pollut</addtitle><description>Decabromodiphenyl ether (BDE-209) has been universally detected in environmental media and animals, but its damage to ovarian function and mechanism is still unclear, and melatonin has been shown to improve mammalian ovarian function. This study aimed to investigate the toxic effects of BDE-209 on the ovary and tried to improve ovarian function with melatonin. Herein, BDE-209 was administered orally to female SD rats for 60 days. Enzyme-linked immunosorbent assay, HE staining, transcriptome analysis, qPCR and immunohistochemical staining were used to explore and verify the potential mechanism. We found that BDE-209 exposure had effects on the ovary, as shown by abnormal changes in the estrous cycle, hormone levels and ovarian reserve function in rats, while increasing the proportion of collagen fibres in ovarian tissue. In terms of mechanism, cuproptosis, a form of cell death, was identified to play a crucial role in BDE-209-induced ovarian dysfunction, with the phenotype manifested as copper salt accumulation in ovary, downregulation of glutathione pathway metabolism and copper transfer molecule (ATP7A/B), and upregulation of FDX1, lipoic acid pathway (LIAS, LIPT1), pyruvate dehydrogenase complex components (DLAT, PDHB, PDHA1), and copper transfer molecule (SLC31A1). Furthermore, possible interventions were explored. Notably, a supplement with melatonin has a repair effect on the damage to ovarian function by reversing the gene expression of cuproptosis-involved molecules. Overall, this study revealed that cuproptosis is involved in BDE-209-induced ovarian damage and the beneficial effect of melatonin on ovarian copper damage, providing evidence for the prevention and control of female reproductive damage induced by BDE-209.
[Display omitted]
•Chronic exposure to BDE-209 leads to abnormal ovarian function.•Cuproptosis plays an important role in BDE-209-induced ovarian dysfunction.•Melatonin can change the expression of cuproptosis-related molecules.•Melatonin can improve the ovarian damage caused by BDE-209.</description><subject>cell death</subject><subject>collagen</subject><subject>Copper</subject><subject>Cuproptosis</subject><subject>decabromodiphenyl ether</subject><subject>Endocrine disrupting chemicals</subject><subject>enzyme-linked immunosorbent assay</subject><subject>estrous cycle</subject><subject>females</subject><subject>gene expression</subject><subject>glutathione</subject><subject>immunohistochemistry</subject><subject>lipoic acid</subject><subject>mammals</subject><subject>Melatonin</subject><subject>metabolism</subject><subject>Ovarian dysfunction</subject><subject>phenotype</subject><subject>pollution</subject><subject>protective effect</subject><subject>pyruvate dehydrogenase (lipoamide)</subject><subject>toxicity</subject><subject>transcriptomics</subject><issn>0269-7491</issn><issn>1873-6424</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkU2L1TAUhoMozp3RfyCSpZte89U23QhyGXVgwI2uQz5OmFzapCZt4f57c-noUiGQQ3jOOeF9EHpHyZES2n08HyFucxqPjDBxpExQQl6gA5U9bzrBxEt0IKwbml4M9AbdlnImhAjO-Wt0w2VPBePsgNbTOuc0L6mEgq8nbmncwNUCO7Da5DQlF-YniJcRw_IEuQnRrbYiadM56Mpdil-jXUKKWEeHK4Tr0AXq0wYYvK8VTh5PMOolxRDfoFdejwXePt936OeX-x-nb83j968Pp8-PjeVCLA1QbSy1wA2XBgbhQArtAOjAWkG0EVo6Tb2xjBpJWGu8Y85p33Hm2g4Mv0Mf9rn1O79WKIuaQrEwjjpCWovitOWt7PtB_h8lLWuHjktWUbGjNqdSMng15zDpfFGUqKsbdVa7G3V1o3Y3te3984bVTOD-Nv2RUYFPOwA1ki1AVsUGiDXqkGuCyqXw7w2_AYu4pbM</recordid><startdate>20240701</startdate><enddate>20240701</enddate><creator>Wang, Ziyan</creator><creator>Zhang, Wei</creator><creator>Huang, Danyang</creator><creator>Kang, Huiwen</creator><creator>Wang, Jingyu</creator><creator>Liu, Ziyan</creator><creator>Jiang, Guangyu</creator><creator>Gao, Ai</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20240701</creationdate><title>Cuproptosis is involved in decabromodiphenyl ether-induced ovarian dysfunction and the protective effect of melatonin</title><author>Wang, Ziyan ; Zhang, Wei ; Huang, Danyang ; Kang, Huiwen ; Wang, Jingyu ; Liu, Ziyan ; Jiang, Guangyu ; Gao, Ai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-e1abc1ce3b38be94de84adee192540ab4a8da1fbc21b8025bfd2ddaf632d56eb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>cell death</topic><topic>collagen</topic><topic>Copper</topic><topic>Cuproptosis</topic><topic>decabromodiphenyl ether</topic><topic>Endocrine disrupting chemicals</topic><topic>enzyme-linked immunosorbent assay</topic><topic>estrous cycle</topic><topic>females</topic><topic>gene expression</topic><topic>glutathione</topic><topic>immunohistochemistry</topic><topic>lipoic acid</topic><topic>mammals</topic><topic>Melatonin</topic><topic>metabolism</topic><topic>Ovarian dysfunction</topic><topic>phenotype</topic><topic>pollution</topic><topic>protective effect</topic><topic>pyruvate dehydrogenase (lipoamide)</topic><topic>toxicity</topic><topic>transcriptomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Ziyan</creatorcontrib><creatorcontrib>Zhang, Wei</creatorcontrib><creatorcontrib>Huang, Danyang</creatorcontrib><creatorcontrib>Kang, Huiwen</creatorcontrib><creatorcontrib>Wang, Jingyu</creatorcontrib><creatorcontrib>Liu, Ziyan</creatorcontrib><creatorcontrib>Jiang, Guangyu</creatorcontrib><creatorcontrib>Gao, Ai</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Environmental pollution (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Ziyan</au><au>Zhang, Wei</au><au>Huang, Danyang</au><au>Kang, Huiwen</au><au>Wang, Jingyu</au><au>Liu, Ziyan</au><au>Jiang, Guangyu</au><au>Gao, Ai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cuproptosis is involved in decabromodiphenyl ether-induced ovarian dysfunction and the protective effect of melatonin</atitle><jtitle>Environmental pollution (1987)</jtitle><addtitle>Environ Pollut</addtitle><date>2024-07-01</date><risdate>2024</risdate><volume>352</volume><spage>124100</spage><epage>124100</epage><pages>124100-124100</pages><artnum>124100</artnum><issn>0269-7491</issn><eissn>1873-6424</eissn><abstract>Decabromodiphenyl ether (BDE-209) has been universally detected in environmental media and animals, but its damage to ovarian function and mechanism is still unclear, and melatonin has been shown to improve mammalian ovarian function. This study aimed to investigate the toxic effects of BDE-209 on the ovary and tried to improve ovarian function with melatonin. Herein, BDE-209 was administered orally to female SD rats for 60 days. Enzyme-linked immunosorbent assay, HE staining, transcriptome analysis, qPCR and immunohistochemical staining were used to explore and verify the potential mechanism. We found that BDE-209 exposure had effects on the ovary, as shown by abnormal changes in the estrous cycle, hormone levels and ovarian reserve function in rats, while increasing the proportion of collagen fibres in ovarian tissue. In terms of mechanism, cuproptosis, a form of cell death, was identified to play a crucial role in BDE-209-induced ovarian dysfunction, with the phenotype manifested as copper salt accumulation in ovary, downregulation of glutathione pathway metabolism and copper transfer molecule (ATP7A/B), and upregulation of FDX1, lipoic acid pathway (LIAS, LIPT1), pyruvate dehydrogenase complex components (DLAT, PDHB, PDHA1), and copper transfer molecule (SLC31A1). Furthermore, possible interventions were explored. Notably, a supplement with melatonin has a repair effect on the damage to ovarian function by reversing the gene expression of cuproptosis-involved molecules. Overall, this study revealed that cuproptosis is involved in BDE-209-induced ovarian damage and the beneficial effect of melatonin on ovarian copper damage, providing evidence for the prevention and control of female reproductive damage induced by BDE-209.
[Display omitted]
•Chronic exposure to BDE-209 leads to abnormal ovarian function.•Cuproptosis plays an important role in BDE-209-induced ovarian dysfunction.•Melatonin can change the expression of cuproptosis-related molecules.•Melatonin can improve the ovarian damage caused by BDE-209.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>38714232</pmid><doi>10.1016/j.envpol.2024.124100</doi><tpages>1</tpages></addata></record> |
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subjects | cell death collagen Copper Cuproptosis decabromodiphenyl ether Endocrine disrupting chemicals enzyme-linked immunosorbent assay estrous cycle females gene expression glutathione immunohistochemistry lipoic acid mammals Melatonin metabolism Ovarian dysfunction phenotype pollution protective effect pyruvate dehydrogenase (lipoamide) toxicity transcriptomics |
title | Cuproptosis is involved in decabromodiphenyl ether-induced ovarian dysfunction and the protective effect of melatonin |
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