Perfluoroundecanoic acid induces DNA damage, reproductive and pathophysiological dysfunctions via oxidative stress in male Swiss mice
Perfluoroundecanoic acid (PFUnA) is an eleven carbon-chain compound that belongs to the perfluoroalkyl carboxylic acid family. It has been detected in the human blood, effluents, and surface/ground waters, but its toxic effects to the DNA and reproductive system remain unclear. This study was aimed...
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creator | Ogunsuyi, Opeoluwa M. Fasakin, Peter T. Ajibiye, Oluwatobi P. Ogunsuyi, Olusegun I. Adekoya, Khalid O. |
description | Perfluoroundecanoic acid (PFUnA) is an eleven carbon-chain compound that belongs to the perfluoroalkyl carboxylic acid family. It has been detected in the human blood, effluents, and surface/ground waters, but its toxic effects to the DNA and reproductive system remain unclear. This study was aimed at exploring the toxicity of PFUnA on the hepatic DNA, organ-system and reproductive system in orally treated male Swiss mice. In this present study, administration of PFUnA for 28 days with five doses (0.1, 0.3, 05, 0.7 and 1.0 mg kg-1 b.w./d) in male Swiss mice induced significant hepatic DNA damage which was observed using the alkaline comet assay and equally altered hematological and clinical biochemical parameters. In addition to testicular atrophy, sperm count and sperm motility significantly decreased while sperm abnormalities increased after 35 days exposure. Serum LH and FSH levels were remarkably increased while serum testosterone levels were strikingly reduced. Histopathology revealed the liver, kidney, and testis as potential targets of PFUnA toxicity. Increased activities of superoxide dismutase (SOD) and catalase (CAT), as well as levels of glutathione-s-transferase (GST) and reduced glutathione (GSH), with consistent reduction of glutathione peroxidase (GPx) and reduced glutathione (GSH) in the liver and testis induced oxidative stress. In conclusion, PFUnA exhibited both genotoxicity and reproductive toxicity via oxidative stress induction.
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•DNA damage, organ-system, and reproductive toxicities of PFUnA were evaluated.•PFUnA induced hepatic DNA damage.•PFUnA toxicities were observed in liver, kidney, testes, and not the spleen.•PFUnA significantly altered the function of the reproductive system.•DNA damage and testicular PFUnA-toxicities were related to ROS generation. |
doi_str_mv | 10.1016/j.chemosphere.2023.139491 |
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[Display omitted]
•DNA damage, organ-system, and reproductive toxicities of PFUnA were evaluated.•PFUnA induced hepatic DNA damage.•PFUnA toxicities were observed in liver, kidney, testes, and not the spleen.•PFUnA significantly altered the function of the reproductive system.•DNA damage and testicular PFUnA-toxicities were related to ROS generation.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2023.139491</identifier><identifier>PMID: 37453524</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Antioxidants - metabolism ; atrophy ; blood serum ; carboxylic acids ; catalase ; Comet assay ; DNA ; DNA Damage ; family ; Fluorocarbons - metabolism ; genotoxicity ; glutathione ; Glutathione - metabolism ; glutathione peroxidase ; glutathione transferase ; histopathology ; Humans ; kidneys ; liver ; Male ; males ; Mice ; Oxidative Stress ; perfluorocarbons ; Perfluoroundecanoic acid ; Reproductive hormones ; reproductive toxicology ; Semen ; Sperm Motility ; Sperm parameters ; Spermatozoa ; superoxide dismutase ; Superoxide Dismutase - metabolism ; testes ; Testis ; testosterone</subject><ispartof>Chemosphere (Oxford), 2023-10, Vol.338, p.139491-139491, Article 139491</ispartof><rights>2023 Elsevier Ltd</rights><rights>Copyright © 2023 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c325t-b9ec77dfbf11844d8fc57b43ff773e05be6a73645dd9c10b8309f3d27a9faa833</citedby><cites>FETCH-LOGICAL-c325t-b9ec77dfbf11844d8fc57b43ff773e05be6a73645dd9c10b8309f3d27a9faa833</cites><orcidid>0000-0001-6685-6029</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0045653523017587$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37453524$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ogunsuyi, Opeoluwa M.</creatorcontrib><creatorcontrib>Fasakin, Peter T.</creatorcontrib><creatorcontrib>Ajibiye, Oluwatobi P.</creatorcontrib><creatorcontrib>Ogunsuyi, Olusegun I.</creatorcontrib><creatorcontrib>Adekoya, Khalid O.</creatorcontrib><title>Perfluoroundecanoic acid induces DNA damage, reproductive and pathophysiological dysfunctions via oxidative stress in male Swiss mice</title><title>Chemosphere (Oxford)</title><addtitle>Chemosphere</addtitle><description>Perfluoroundecanoic acid (PFUnA) is an eleven carbon-chain compound that belongs to the perfluoroalkyl carboxylic acid family. It has been detected in the human blood, effluents, and surface/ground waters, but its toxic effects to the DNA and reproductive system remain unclear. This study was aimed at exploring the toxicity of PFUnA on the hepatic DNA, organ-system and reproductive system in orally treated male Swiss mice. In this present study, administration of PFUnA for 28 days with five doses (0.1, 0.3, 05, 0.7 and 1.0 mg kg-1 b.w./d) in male Swiss mice induced significant hepatic DNA damage which was observed using the alkaline comet assay and equally altered hematological and clinical biochemical parameters. In addition to testicular atrophy, sperm count and sperm motility significantly decreased while sperm abnormalities increased after 35 days exposure. Serum LH and FSH levels were remarkably increased while serum testosterone levels were strikingly reduced. Histopathology revealed the liver, kidney, and testis as potential targets of PFUnA toxicity. Increased activities of superoxide dismutase (SOD) and catalase (CAT), as well as levels of glutathione-s-transferase (GST) and reduced glutathione (GSH), with consistent reduction of glutathione peroxidase (GPx) and reduced glutathione (GSH) in the liver and testis induced oxidative stress. In conclusion, PFUnA exhibited both genotoxicity and reproductive toxicity via oxidative stress induction.
[Display omitted]
•DNA damage, organ-system, and reproductive toxicities of PFUnA were evaluated.•PFUnA induced hepatic DNA damage.•PFUnA toxicities were observed in liver, kidney, testes, and not the spleen.•PFUnA significantly altered the function of the reproductive system.•DNA damage and testicular PFUnA-toxicities were related to ROS generation.</description><subject>Animals</subject><subject>Antioxidants - metabolism</subject><subject>atrophy</subject><subject>blood serum</subject><subject>carboxylic acids</subject><subject>catalase</subject><subject>Comet assay</subject><subject>DNA</subject><subject>DNA Damage</subject><subject>family</subject><subject>Fluorocarbons - metabolism</subject><subject>genotoxicity</subject><subject>glutathione</subject><subject>Glutathione - metabolism</subject><subject>glutathione peroxidase</subject><subject>glutathione transferase</subject><subject>histopathology</subject><subject>Humans</subject><subject>kidneys</subject><subject>liver</subject><subject>Male</subject><subject>males</subject><subject>Mice</subject><subject>Oxidative Stress</subject><subject>perfluorocarbons</subject><subject>Perfluoroundecanoic acid</subject><subject>Reproductive hormones</subject><subject>reproductive toxicology</subject><subject>Semen</subject><subject>Sperm Motility</subject><subject>Sperm parameters</subject><subject>Spermatozoa</subject><subject>superoxide dismutase</subject><subject>Superoxide Dismutase - metabolism</subject><subject>testes</subject><subject>Testis</subject><subject>testosterone</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkdFuFCEUhomxsWv1FQzeeeFsYYAZuGy2Vk2a1kS9JgwcumxmhhFmVvcBfO9Stxrv9Ipw8v3_CXwIvaZkTQltzndru4Uh5mkLCdY1qdmaMsUVfYJWVLaqorWST9GKEC6qRjBxip7nvCOkhIV6hk5Zy8u05iv08xMk3y8xxWV0YM0Yg8XGBofD6BYLGV_eXGBnBnMHb3GCKcUynsMesBkdnsy8jdP2kEPs412wpsfukP0yFiSOGe-DwfFHcOZXIs8Jci7NeDA94M_fQ7kNwcILdOJNn-Hl43mGvl69-7L5UF3fvv-4ubiuLKvFXHUKbNs633lKJedOeivajjPv25YBER00pmUNF84pS0knGVGeubo1yhsjGTtDb4695RnfFsizHkK20PdmhLhkXUuupBKi1P0bZbIWnDWkoOqI2hRzTuD1lMJg0kFToh-E6Z3-S5h-EKaPwkr21eOapRvA_Un-NlSAzRGA8i_7AElnG2C04EICO2sXw3-suQdrKbCB</recordid><startdate>202310</startdate><enddate>202310</enddate><creator>Ogunsuyi, Opeoluwa M.</creator><creator>Fasakin, Peter T.</creator><creator>Ajibiye, Oluwatobi P.</creator><creator>Ogunsuyi, Olusegun I.</creator><creator>Adekoya, Khalid O.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0001-6685-6029</orcidid></search><sort><creationdate>202310</creationdate><title>Perfluoroundecanoic acid induces DNA damage, reproductive and pathophysiological dysfunctions via oxidative stress in male Swiss mice</title><author>Ogunsuyi, Opeoluwa M. ; Fasakin, Peter T. ; Ajibiye, Oluwatobi P. ; Ogunsuyi, Olusegun I. ; Adekoya, Khalid O.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c325t-b9ec77dfbf11844d8fc57b43ff773e05be6a73645dd9c10b8309f3d27a9faa833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Antioxidants - metabolism</topic><topic>atrophy</topic><topic>blood serum</topic><topic>carboxylic acids</topic><topic>catalase</topic><topic>Comet assay</topic><topic>DNA</topic><topic>DNA Damage</topic><topic>family</topic><topic>Fluorocarbons - metabolism</topic><topic>genotoxicity</topic><topic>glutathione</topic><topic>Glutathione - metabolism</topic><topic>glutathione peroxidase</topic><topic>glutathione transferase</topic><topic>histopathology</topic><topic>Humans</topic><topic>kidneys</topic><topic>liver</topic><topic>Male</topic><topic>males</topic><topic>Mice</topic><topic>Oxidative Stress</topic><topic>perfluorocarbons</topic><topic>Perfluoroundecanoic acid</topic><topic>Reproductive hormones</topic><topic>reproductive toxicology</topic><topic>Semen</topic><topic>Sperm Motility</topic><topic>Sperm parameters</topic><topic>Spermatozoa</topic><topic>superoxide dismutase</topic><topic>Superoxide Dismutase - metabolism</topic><topic>testes</topic><topic>Testis</topic><topic>testosterone</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ogunsuyi, Opeoluwa M.</creatorcontrib><creatorcontrib>Fasakin, Peter T.</creatorcontrib><creatorcontrib>Ajibiye, Oluwatobi P.</creatorcontrib><creatorcontrib>Ogunsuyi, Olusegun I.</creatorcontrib><creatorcontrib>Adekoya, Khalid O.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ogunsuyi, Opeoluwa M.</au><au>Fasakin, Peter T.</au><au>Ajibiye, Oluwatobi P.</au><au>Ogunsuyi, Olusegun I.</au><au>Adekoya, Khalid O.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Perfluoroundecanoic acid induces DNA damage, reproductive and pathophysiological dysfunctions via oxidative stress in male Swiss mice</atitle><jtitle>Chemosphere (Oxford)</jtitle><addtitle>Chemosphere</addtitle><date>2023-10</date><risdate>2023</risdate><volume>338</volume><spage>139491</spage><epage>139491</epage><pages>139491-139491</pages><artnum>139491</artnum><issn>0045-6535</issn><eissn>1879-1298</eissn><abstract>Perfluoroundecanoic acid (PFUnA) is an eleven carbon-chain compound that belongs to the perfluoroalkyl carboxylic acid family. It has been detected in the human blood, effluents, and surface/ground waters, but its toxic effects to the DNA and reproductive system remain unclear. This study was aimed at exploring the toxicity of PFUnA on the hepatic DNA, organ-system and reproductive system in orally treated male Swiss mice. In this present study, administration of PFUnA for 28 days with five doses (0.1, 0.3, 05, 0.7 and 1.0 mg kg-1 b.w./d) in male Swiss mice induced significant hepatic DNA damage which was observed using the alkaline comet assay and equally altered hematological and clinical biochemical parameters. In addition to testicular atrophy, sperm count and sperm motility significantly decreased while sperm abnormalities increased after 35 days exposure. Serum LH and FSH levels were remarkably increased while serum testosterone levels were strikingly reduced. Histopathology revealed the liver, kidney, and testis as potential targets of PFUnA toxicity. Increased activities of superoxide dismutase (SOD) and catalase (CAT), as well as levels of glutathione-s-transferase (GST) and reduced glutathione (GSH), with consistent reduction of glutathione peroxidase (GPx) and reduced glutathione (GSH) in the liver and testis induced oxidative stress. In conclusion, PFUnA exhibited both genotoxicity and reproductive toxicity via oxidative stress induction.
[Display omitted]
•DNA damage, organ-system, and reproductive toxicities of PFUnA were evaluated.•PFUnA induced hepatic DNA damage.•PFUnA toxicities were observed in liver, kidney, testes, and not the spleen.•PFUnA significantly altered the function of the reproductive system.•DNA damage and testicular PFUnA-toxicities were related to ROS generation.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>37453524</pmid><doi>10.1016/j.chemosphere.2023.139491</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-6685-6029</orcidid></addata></record> |
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subjects | Animals Antioxidants - metabolism atrophy blood serum carboxylic acids catalase Comet assay DNA DNA Damage family Fluorocarbons - metabolism genotoxicity glutathione Glutathione - metabolism glutathione peroxidase glutathione transferase histopathology Humans kidneys liver Male males Mice Oxidative Stress perfluorocarbons Perfluoroundecanoic acid Reproductive hormones reproductive toxicology Semen Sperm Motility Sperm parameters Spermatozoa superoxide dismutase Superoxide Dismutase - metabolism testes Testis testosterone |
title | Perfluoroundecanoic acid induces DNA damage, reproductive and pathophysiological dysfunctions via oxidative stress in male Swiss mice |
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