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
Hauptverfasser: Wang, Ziyan, Zhang, Wei, Huang, Danyang, Kang, Huiwen, Wang, Jingyu, Liu, Ziyan, Jiang, Guangyu, Gao, Ai
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container_end_page 124100
container_issue
container_start_page 124100
container_title Environmental pollution (1987)
container_volume 352
creator Wang, Ziyan
Zhang, Wei
Huang, Danyang
Kang, Huiwen
Wang, Jingyu
Liu, Ziyan
Jiang, Guangyu
Gao, Ai
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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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><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. 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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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ispartof Environmental pollution (1987), 2024-07, Vol.352, p.124100-124100, Article 124100
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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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