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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Veröffentlicht in:Chemosphere (Oxford) 2023-10, Vol.338, p.139491-139491, Article 139491
Hauptverfasser: Ogunsuyi, Opeoluwa M., Fasakin, Peter T., Ajibiye, Oluwatobi P., Ogunsuyi, Olusegun I., Adekoya, Khalid O.
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container_title Chemosphere (Oxford)
container_volume 338
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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. [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.
doi_str_mv 10.1016/j.chemosphere.2023.139491
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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><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. 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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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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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