Exploring the endocrine disrupting potential of a complex mixture of PAHs in the estrogen pathway in Oreochromis niloticus hepatocytes

•Oreochromis niloticus hepatocytes were exposed to a mixture of PAHs.•Exposure affected the expression of genes related to the estrogen pathway.•Vtg expression increased 120% in response to PAH exposure.•Antioxidant defense system responded to PAH exposure.•Multixenobiotic resistance-associated prot...

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Veröffentlicht in:Aquatic toxicology 2024-08, Vol.273, p.107002, Article 107002
Hauptverfasser: de Souza, Tugstênio Lima, da Luz, Jessica Zablocki, Roque, Aliciane de Almeida, Opuskevitch, Iracema, Ferreira, Fernando Cesar Alves da Silva, Ribeiro, Ciro Alberto de Oliveira, Neto, Francisco Filipak
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container_start_page 107002
container_title Aquatic toxicology
container_volume 273
creator de Souza, Tugstênio Lima
da Luz, Jessica Zablocki
Roque, Aliciane de Almeida
Opuskevitch, Iracema
Ferreira, Fernando Cesar Alves da Silva
Ribeiro, Ciro Alberto de Oliveira
Neto, Francisco Filipak
description •Oreochromis niloticus hepatocytes were exposed to a mixture of PAHs.•Exposure affected the expression of genes related to the estrogen pathway.•Vtg expression increased 120% in response to PAH exposure.•Antioxidant defense system responded to PAH exposure.•Multixenobiotic resistance-associated proteins activity increased. This study aimed to investigate the toxicity and endocrine disrupting potential of a complex mixture of polycyclic aromatic hydrocarbons (PAHs) in the estrogen pathway using hepatocytes of Nile tilapia Oreochromis niloticus, the hepatocytes were exposed to various concentrations of the PAH mixture, and multiple endpoints were evaluated to assess their effects on cell viability, gene expression, oxidative stress markers, and efflux activity. The results revealed that the PAH mixture had limited effects on hepatocyte metabolism and cell adhesion, as indicated by the non-significant changes observed in MTT metabolism, neutral red retention, and crystal violet staining. However, significant alterations were observed in the expression of genes related to the estrogen pathway. Specifically, vitellogenin (vtg) exhibited a substantial increase of approximately 120% compared to the control group. Similarly, estrogen receptor 2 (esr2) showed a significant upregulation of approximately 90%. In contrast, no significant differences were observed in the expression of estrogen receptor 1 (esr1) and the G protein-coupled estrogen receptor 1 (gper1). Furthermore, the PAH mixture elicited complex responses in oxidative stress markers. While reactive oxygen species (ROS) and reactive nitrogen species (RNS) levels remained unchanged, the activity of catalase (Cat) was significantly reduced, whereas superoxide dismutase (Sod) activity, glutathione S-transferase (Gst) activity, and non-protein thiols levels were significantly elevated. In addition, the PAH mixture significantly influenced efflux activity, as evidenced by the increased efflux of rhodamine and calcein, indicating alterations in multixenobiotic resistance (MXR)-associated proteins. Overall, these findings, associated with bioinformatic analysis, highlight the potential of the PAH mixture to modulate the estrogen pathway and induce oxidative stress in O. niloticus hepatocytes. Understanding the mechanisms underlying these effects is crucial for assessing the ecological risks of PAH exposure and developing appropriate strategies to mitigate their adverse impacts on aquatic organisms.
doi_str_mv 10.1016/j.aquatox.2024.107002
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This study aimed to investigate the toxicity and endocrine disrupting potential of a complex mixture of polycyclic aromatic hydrocarbons (PAHs) in the estrogen pathway using hepatocytes of Nile tilapia Oreochromis niloticus, the hepatocytes were exposed to various concentrations of the PAH mixture, and multiple endpoints were evaluated to assess their effects on cell viability, gene expression, oxidative stress markers, and efflux activity. The results revealed that the PAH mixture had limited effects on hepatocyte metabolism and cell adhesion, as indicated by the non-significant changes observed in MTT metabolism, neutral red retention, and crystal violet staining. However, significant alterations were observed in the expression of genes related to the estrogen pathway. Specifically, vitellogenin (vtg) exhibited a substantial increase of approximately 120% compared to the control group. Similarly, estrogen receptor 2 (esr2) showed a significant upregulation of approximately 90%. In contrast, no significant differences were observed in the expression of estrogen receptor 1 (esr1) and the G protein-coupled estrogen receptor 1 (gper1). Furthermore, the PAH mixture elicited complex responses in oxidative stress markers. While reactive oxygen species (ROS) and reactive nitrogen species (RNS) levels remained unchanged, the activity of catalase (Cat) was significantly reduced, whereas superoxide dismutase (Sod) activity, glutathione S-transferase (Gst) activity, and non-protein thiols levels were significantly elevated. In addition, the PAH mixture significantly influenced efflux activity, as evidenced by the increased efflux of rhodamine and calcein, indicating alterations in multixenobiotic resistance (MXR)-associated proteins. Overall, these findings, associated with bioinformatic analysis, highlight the potential of the PAH mixture to modulate the estrogen pathway and induce oxidative stress in O. niloticus hepatocytes. 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This study aimed to investigate the toxicity and endocrine disrupting potential of a complex mixture of polycyclic aromatic hydrocarbons (PAHs) in the estrogen pathway using hepatocytes of Nile tilapia Oreochromis niloticus, the hepatocytes were exposed to various concentrations of the PAH mixture, and multiple endpoints were evaluated to assess their effects on cell viability, gene expression, oxidative stress markers, and efflux activity. The results revealed that the PAH mixture had limited effects on hepatocyte metabolism and cell adhesion, as indicated by the non-significant changes observed in MTT metabolism, neutral red retention, and crystal violet staining. However, significant alterations were observed in the expression of genes related to the estrogen pathway. Specifically, vitellogenin (vtg) exhibited a substantial increase of approximately 120% compared to the control group. Similarly, estrogen receptor 2 (esr2) showed a significant upregulation of approximately 90%. In contrast, no significant differences were observed in the expression of estrogen receptor 1 (esr1) and the G protein-coupled estrogen receptor 1 (gper1). Furthermore, the PAH mixture elicited complex responses in oxidative stress markers. While reactive oxygen species (ROS) and reactive nitrogen species (RNS) levels remained unchanged, the activity of catalase (Cat) was significantly reduced, whereas superoxide dismutase (Sod) activity, glutathione S-transferase (Gst) activity, and non-protein thiols levels were significantly elevated. In addition, the PAH mixture significantly influenced efflux activity, as evidenced by the increased efflux of rhodamine and calcein, indicating alterations in multixenobiotic resistance (MXR)-associated proteins. Overall, these findings, associated with bioinformatic analysis, highlight the potential of the PAH mixture to modulate the estrogen pathway and induce oxidative stress in O. niloticus hepatocytes. Understanding the mechanisms underlying these effects is crucial for assessing the ecological risks of PAH exposure and developing appropriate strategies to mitigate their adverse impacts on aquatic organisms.</description><subject>Bioinformatics</subject><subject>Nile tilapia</subject><subject>Oxidative stress</subject><subject>Primary hepatocyte</subject><subject>Vitellogenin</subject><issn>0166-445X</issn><issn>1879-1514</issn><issn>1879-1514</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkctO3DAUhi1EBcPlEUBessngW5LJCiFEAQmJLlqpO8uxTxiPkjjYDsy8AM9dRxnY1psj__7OxedH6IKSJSW0uN4s1duootsuGWEiaSUh7AAt6KqsMppTcYgWiSsyIfK_x-gkhA1Jh4nqCB3zVcULJtgCfd5vh9Z527_iuAYMvXE63QAbG_w4xOlhcBH6aFWLXYMV1q4bWtjizm7j6GESf90-Bmz7uUSI3r1CjwcV1x9qN-kvHpxee9fZgHvbumj1GPAaEuL0LkI4Qz8a1QY438dT9Ofn_e-7x-z55eHp7vY500zwmIkVo2WteUE4bVShqAGT01zXORNCNLQsgTdCkYYpZXRFDK05kDIvuWj0itT8FF3NdQfv3sY0qkwjaWhb1YMbg-Sk5IyTirCE5jOqvQvBQyMHbzvld5ISOVkgN3JvgZwskLMFKe9y32KsOzDfWV87T8DNDED66LsFL4O20Gsw1oOO0jj7nxb_AFxWnY0</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>de Souza, Tugstênio Lima</creator><creator>da Luz, Jessica Zablocki</creator><creator>Roque, Aliciane de Almeida</creator><creator>Opuskevitch, Iracema</creator><creator>Ferreira, Fernando Cesar Alves da Silva</creator><creator>Ribeiro, Ciro Alberto de Oliveira</creator><creator>Neto, Francisco Filipak</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3682-4434</orcidid></search><sort><creationdate>20240801</creationdate><title>Exploring the endocrine disrupting potential of a complex mixture of PAHs in the estrogen pathway in Oreochromis niloticus hepatocytes</title><author>de Souza, Tugstênio Lima ; da Luz, Jessica Zablocki ; Roque, Aliciane de Almeida ; Opuskevitch, Iracema ; Ferreira, Fernando Cesar Alves da Silva ; Ribeiro, Ciro Alberto de Oliveira ; Neto, Francisco Filipak</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c243t-48217bc36031fa6a1ded515cb52444f177e3f4a0f2aadc90d1b3e075734fc80b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Bioinformatics</topic><topic>Nile tilapia</topic><topic>Oxidative stress</topic><topic>Primary hepatocyte</topic><topic>Vitellogenin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Souza, Tugstênio Lima</creatorcontrib><creatorcontrib>da Luz, Jessica Zablocki</creatorcontrib><creatorcontrib>Roque, Aliciane de Almeida</creatorcontrib><creatorcontrib>Opuskevitch, Iracema</creatorcontrib><creatorcontrib>Ferreira, Fernando Cesar Alves da Silva</creatorcontrib><creatorcontrib>Ribeiro, Ciro Alberto de Oliveira</creatorcontrib><creatorcontrib>Neto, Francisco Filipak</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Aquatic toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Souza, Tugstênio Lima</au><au>da Luz, Jessica Zablocki</au><au>Roque, Aliciane de Almeida</au><au>Opuskevitch, Iracema</au><au>Ferreira, Fernando Cesar Alves da Silva</au><au>Ribeiro, Ciro Alberto de Oliveira</au><au>Neto, Francisco Filipak</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exploring the endocrine disrupting potential of a complex mixture of PAHs in the estrogen pathway in Oreochromis niloticus hepatocytes</atitle><jtitle>Aquatic toxicology</jtitle><addtitle>Aquat Toxicol</addtitle><date>2024-08-01</date><risdate>2024</risdate><volume>273</volume><spage>107002</spage><pages>107002-</pages><artnum>107002</artnum><issn>0166-445X</issn><issn>1879-1514</issn><eissn>1879-1514</eissn><abstract>•Oreochromis niloticus hepatocytes were exposed to a mixture of PAHs.•Exposure affected the expression of genes related to the estrogen pathway.•Vtg expression increased 120% in response to PAH exposure.•Antioxidant defense system responded to PAH exposure.•Multixenobiotic resistance-associated proteins activity increased. This study aimed to investigate the toxicity and endocrine disrupting potential of a complex mixture of polycyclic aromatic hydrocarbons (PAHs) in the estrogen pathway using hepatocytes of Nile tilapia Oreochromis niloticus, the hepatocytes were exposed to various concentrations of the PAH mixture, and multiple endpoints were evaluated to assess their effects on cell viability, gene expression, oxidative stress markers, and efflux activity. The results revealed that the PAH mixture had limited effects on hepatocyte metabolism and cell adhesion, as indicated by the non-significant changes observed in MTT metabolism, neutral red retention, and crystal violet staining. However, significant alterations were observed in the expression of genes related to the estrogen pathway. Specifically, vitellogenin (vtg) exhibited a substantial increase of approximately 120% compared to the control group. Similarly, estrogen receptor 2 (esr2) showed a significant upregulation of approximately 90%. In contrast, no significant differences were observed in the expression of estrogen receptor 1 (esr1) and the G protein-coupled estrogen receptor 1 (gper1). Furthermore, the PAH mixture elicited complex responses in oxidative stress markers. While reactive oxygen species (ROS) and reactive nitrogen species (RNS) levels remained unchanged, the activity of catalase (Cat) was significantly reduced, whereas superoxide dismutase (Sod) activity, glutathione S-transferase (Gst) activity, and non-protein thiols levels were significantly elevated. In addition, the PAH mixture significantly influenced efflux activity, as evidenced by the increased efflux of rhodamine and calcein, indicating alterations in multixenobiotic resistance (MXR)-associated proteins. Overall, these findings, associated with bioinformatic analysis, highlight the potential of the PAH mixture to modulate the estrogen pathway and induce oxidative stress in O. niloticus hepatocytes. Understanding the mechanisms underlying these effects is crucial for assessing the ecological risks of PAH exposure and developing appropriate strategies to mitigate their adverse impacts on aquatic organisms.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38936242</pmid><doi>10.1016/j.aquatox.2024.107002</doi><orcidid>https://orcid.org/0000-0003-3682-4434</orcidid></addata></record>
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subjects Bioinformatics
Nile tilapia
Oxidative stress
Primary hepatocyte
Vitellogenin
title Exploring the endocrine disrupting potential of a complex mixture of PAHs in the estrogen pathway in Oreochromis niloticus hepatocytes
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