Mixtures of benzo(a)pyrene, dichlorodiphenyltrichloroethane and tributyltin are more toxic to neotropical fish Rhamdia quelen than isolated exposures

The effects of benzo(a)pyrene (BaP), dichlorodiphenyltrichloroethane (DDT) and tributyltin (TBT) association were investigated through a multi-biomarker approach. Ten Rhamdia quelen fish per group were exposed through intraperitoneal injections either to BaP (0.3; 3 or 30mgkg−1), DDT or TBT (0.03; 0...

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Published inEcotoxicology and environmental safety Vol. 122; pp. 106 - 115
Main Authors Oliveira, Heloísa H.P., Liebel, Samuel, Rossi, Stéfani C., Azevedo, Ana C.B., Barrera, Ellie A.L., Garcia, Juan Ramon Esquivel, Grötzner, Sônia Regina, Neto, Francisco Filipak, Randi, Marco A.F., Ribeiro, Ciro A.O.
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LanguageEnglish
Published Netherlands Elsevier Inc 01.12.2015
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Abstract The effects of benzo(a)pyrene (BaP), dichlorodiphenyltrichloroethane (DDT) and tributyltin (TBT) association were investigated through a multi-biomarker approach. Ten Rhamdia quelen fish per group were exposed through intraperitoneal injections either to BaP (0.3; 3 or 30mgkg−1), DDT or TBT (0.03; 0.3 or 3mgkg−1) or BaP/DDT, BaP/TBT, DDT/TBT or BaP/DDT/TBT on their lowest doses. The experiments were divided in acute (one dose, 5-day) and sub-chronic (3 doses, 15-day). Control groups received an equal volume of PBS or canola oil (1mlkg−1). The three tested contaminants altered AChE activity in brain and muscle in similar ways; the mixtures antagonized the increase evoked by the contaminants alone. BaP and TBT increased GSH content and mixtures reduced it. GPx activity was increased by DDT and TBT in the 15-day experiment and reduced by the mixtures. BaP increased GST activity in sub-chronic experiment while TBT reduced it in the acute experiment. BaP/TBT increased GST activity compared to all groups; the other mixtures reduced it compared to BaP or DDT in the 5-day experiment. BaP, DDT and TBT increased δ-ALAd activity mainly in acute exposure; the mixtures also increased δ-ALAd compared to DDT or TBT in 5 and 15-day. BaP, TBT and BaP/DDT decreased LPO in the acute experiment. In the sub-chronic experiment DDT/TBT increased LPO when compared to TBT. None of the contaminants alone altered PCO, but all mixtures increased it compared to one or another contaminant. Contaminants isolated had a more acute effect in ALT plasma level; their lowest dose, which had no effect alone, in combination has led to an increase of this enzyme, especially after 15 days. DDT increased AST in the acute and sub-chronic experiments, while TBT did the same in the latter. DDT/TBT decreased AST opposing the effect of the contaminants alone in the 5-day experiment. Hepatic lesions index could be explained by a more acute effect of the contaminants alone or combined and by activation of cell defenses after the sub-chronic exposure. TBT increased melanomacrophages counting in the 5-day experiment and the mixtures increased it in the 5 and 15-day experiments. Overall, the majority of the biomarkers pointed to a more toxic effect when these contaminants were combined, leading to unexpected toxicities compared to individual exposure scenarios. These findings are relevant considering environmental exposure conditions, since organisms are often exposed to different combinations of contaminants. •Effects of BaP, DDT and TBT in fish were assessed through a multibiomarker approach.•Oxidative stress, neurotoxicity and hepatotoxicity biomarkers were analyzed.•Fish were exposed to BaP, DDT and TBT alone or combined.•Results pointed to a more toxic effect when these contaminants were combined.•Mixtures potentialize or promote effects opposite to those of contaminants alone.
AbstractList The effects of benzo(a)pyrene (BaP), dichlorodiphenyltrichloroethane (DDT) and tributyltin (TBT) association were investigated through a multi-biomarker approach. Ten Rhamdia quelen fish per group were exposed through intraperitoneal injections either to BaP (0.3; 3 or 30mgkg-1), DDT or TBT (0.03; 0.3 or 3mgkg-1) or BaP/DDT, BaP/TBT, DDT/TBT or BaP/DDT/TBT on their lowest doses. The experiments were divided in acute (one dose, 5-day) and sub-chronic (3 doses, 15-day). Control groups received an equal volume of PBS or canola oil (1mlkg-1). The three tested contaminants altered AChE activity in brain and muscle in similar ways; the mixtures antagonized the increase evoked by the contaminants alone. BaP and TBT increased GSH content and mixtures reduced it. GPx activity was increased by DDT and TBT in the 15-day experiment and reduced by the mixtures. BaP increased GST activity in sub-chronic experiment while TBT reduced it in the acute experiment. BaP/TBT increased GST activity compared to all groups; the other mixtures reduced it compared to BaP or DDT in the 5-day experiment. BaP, DDT and TBT increased delta -ALAd activity mainly in acute exposure; the mixtures also increased delta -ALAd compared to DDT or TBT in 5 and 15-day. BaP, TBT and BaP/DDT decreased LPO in the acute experiment. In the sub-chronic experiment DDT/TBT increased LPO when compared to TBT. None of the contaminants alone altered PCO, but all mixtures increased it compared to one or another contaminant. Contaminants isolated had a more acute effect in ALT plasma level; their lowest dose, which had no effect alone, in combination has led to an increase of this enzyme, especially after 15 days. DDT increased AST in the acute and sub-chronic experiments, while TBT did the same in the latter. DDT/TBT decreased AST opposing the effect of the contaminants alone in the 5-day experiment. Hepatic lesions index could be explained by a more acute effect of the contaminants alone or combined and by activation of cell defenses after the sub-chronic exposure. TBT increased melanomacrophages counting in the 5-day experiment and the mixtures increased it in the 5 and 15-day experiments. Overall, the majority of the biomarkers pointed to a more toxic effect when these contaminants were combined, leading to unexpected toxicities compared to individual exposure scenarios. These findings are relevant considering environmental exposure conditions, since organisms are often exposed to different combinations of contaminants.
The effects of benzo(a)pyrene (BaP), dichlorodiphenyltrichloroethane (DDT) and tributyltin (TBT) association were investigated through a multi-biomarker approach. Ten Rhamdia quelen fish per group were exposed through intraperitoneal injections either to BaP (0.3; 3 or 30mgkg−1), DDT or TBT (0.03; 0.3 or 3mgkg−1) or BaP/DDT, BaP/TBT, DDT/TBT or BaP/DDT/TBT on their lowest doses. The experiments were divided in acute (one dose, 5-day) and sub-chronic (3 doses, 15-day). Control groups received an equal volume of PBS or canola oil (1mlkg−1). The three tested contaminants altered AChE activity in brain and muscle in similar ways; the mixtures antagonized the increase evoked by the contaminants alone. BaP and TBT increased GSH content and mixtures reduced it. GPx activity was increased by DDT and TBT in the 15-day experiment and reduced by the mixtures. BaP increased GST activity in sub-chronic experiment while TBT reduced it in the acute experiment. BaP/TBT increased GST activity compared to all groups; the other mixtures reduced it compared to BaP or DDT in the 5-day experiment. BaP, DDT and TBT increased δ-ALAd activity mainly in acute exposure; the mixtures also increased δ-ALAd compared to DDT or TBT in 5 and 15-day. BaP, TBT and BaP/DDT decreased LPO in the acute experiment. In the sub-chronic experiment DDT/TBT increased LPO when compared to TBT. None of the contaminants alone altered PCO, but all mixtures increased it compared to one or another contaminant. Contaminants isolated had a more acute effect in ALT plasma level; their lowest dose, which had no effect alone, in combination has led to an increase of this enzyme, especially after 15 days. DDT increased AST in the acute and sub-chronic experiments, while TBT did the same in the latter. DDT/TBT decreased AST opposing the effect of the contaminants alone in the 5-day experiment. Hepatic lesions index could be explained by a more acute effect of the contaminants alone or combined and by activation of cell defenses after the sub-chronic exposure. TBT increased melanomacrophages counting in the 5-day experiment and the mixtures increased it in the 5 and 15-day experiments. Overall, the majority of the biomarkers pointed to a more toxic effect when these contaminants were combined, leading to unexpected toxicities compared to individual exposure scenarios. These findings are relevant considering environmental exposure conditions, since organisms are often exposed to different combinations of contaminants. •Effects of BaP, DDT and TBT in fish were assessed through a multibiomarker approach.•Oxidative stress, neurotoxicity and hepatotoxicity biomarkers were analyzed.•Fish were exposed to BaP, DDT and TBT alone or combined.•Results pointed to a more toxic effect when these contaminants were combined.•Mixtures potentialize or promote effects opposite to those of contaminants alone.
The effects of benzo(a)pyrene (BaP), dichlorodiphenyltrichloroethane (DDT) and tributyltin (TBT) association were investigated through a multi-biomarker approach. Ten Rhamdia quelen fish per group were exposed through intraperitoneal injections either to BaP (0.3; 3 or 30 mg kg(-1)), DDT or TBT (0.03; 0.3 or 3 mg kg(-1)) or BaP/DDT, BaP/TBT, DDT/TBT or BaP/DDT/TBT on their lowest doses. The experiments were divided in acute (one dose, 5-day) and sub-chronic (3 doses, 15-day). Control groups received an equal volume of PBS or canola oil (1 ml kg(-1)). The three tested contaminants altered AChE activity in brain and muscle in similar ways; the mixtures antagonized the increase evoked by the contaminants alone. BaP and TBT increased GSH content and mixtures reduced it. GPx activity was increased by DDT and TBT in the 15-day experiment and reduced by the mixtures. BaP increased GST activity in sub-chronic experiment while TBT reduced it in the acute experiment. BaP/TBT increased GST activity compared to all groups; the other mixtures reduced it compared to BaP or DDT in the 5-day experiment. BaP, DDT and TBT increased δ-ALAd activity mainly in acute exposure; the mixtures also increased δ-ALAd compared to DDT or TBT in 5 and 15-day. BaP, TBT and BaP/DDT decreased LPO in the acute experiment. In the sub-chronic experiment DDT/TBT increased LPO when compared to TBT. None of the contaminants alone altered PCO, but all mixtures increased it compared to one or another contaminant. Contaminants isolated had a more acute effect in ALT plasma level; their lowest dose, which had no effect alone, in combination has led to an increase of this enzyme, especially after 15 days. DDT increased AST in the acute and sub-chronic experiments, while TBT did the same in the latter. DDT/TBT decreased AST opposing the effect of the contaminants alone in the 5-day experiment. Hepatic lesions index could be explained by a more acute effect of the contaminants alone or combined and by activation of cell defenses after the sub-chronic exposure. TBT increased melanomacrophages counting in the 5-day experiment and the mixtures increased it in the 5 and 15-day experiments. Overall, the majority of the biomarkers pointed to a more toxic effect when these contaminants were combined, leading to unexpected toxicities compared to individual exposure scenarios. These findings are relevant considering environmental exposure conditions, since organisms are often exposed to different combinations of contaminants.
Author Garcia, Juan Ramon Esquivel
Ribeiro, Ciro A.O.
Azevedo, Ana C.B.
Oliveira, Heloísa H.P.
Rossi, Stéfani C.
Randi, Marco A.F.
Liebel, Samuel
Neto, Francisco Filipak
Grötzner, Sônia Regina
Barrera, Ellie A.L.
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  organization: Departamento de Biologia Celular, Universidade Federal do Paraná, Caixa Postal 19.031, CEP 81.531-990, Curitiba, PR, Brazil
– sequence: 2
  givenname: Samuel
  surname: Liebel
  fullname: Liebel, Samuel
  email: samliebel@yahoo.com.br
  organization: Departamento de Biologia Celular, Universidade Federal do Paraná, Caixa Postal 19.031, CEP 81.531-990, Curitiba, PR, Brazil
– sequence: 3
  givenname: Stéfani C.
  surname: Rossi
  fullname: Rossi, Stéfani C.
  email: ste_bio@yahoo.com.br
  organization: Departamento de Farmacologia, Universidade Federal do Paraná, Caixa Postal 19.031, CEP 81.531-990, Curitiba, PR, Brazil
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  surname: Azevedo
  fullname: Azevedo, Ana C.B.
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  organization: Departamento de Biologia Celular, Universidade Federal do Paraná, Caixa Postal 19.031, CEP 81.531-990, Curitiba, PR, Brazil
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  givenname: Ellie A.L.
  surname: Barrera
  fullname: Barrera, Ellie A.L.
  email: bellotalopez@gmail.com
  organization: Departamento de Ecologia, Universidade Federal do Paraná, Caixa Postal 19.031, CEP 81.531-990, Curitiba, PR, Brazil
– sequence: 6
  givenname: Juan Ramon Esquivel
  surname: Garcia
  fullname: Garcia, Juan Ramon Esquivel
  email: juan.esquivel@unisul.br
  organization: Estação de Piscicultura Panamá, Est. Geral Bom Retiro, km 8, Caixa Postal 03, CEP 88.490-000, Paulo Lopes, SC, Brazil
– sequence: 7
  givenname: Sônia Regina
  surname: Grötzner
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– sequence: 8
  givenname: Francisco Filipak
  surname: Neto
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  givenname: Marco A.F.
  surname: Randi
  fullname: Randi, Marco A.F.
  email: mafrandi@ufpr.br
  organization: Departamento de Biologia Celular, Universidade Federal do Paraná, Caixa Postal 19.031, CEP 81.531-990, Curitiba, PR, Brazil
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  givenname: Ciro A.O.
  surname: Ribeiro
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Keywords Biomarker
Histopathology
Organic pollutant
Toxicity
Mixture
Neotropical fish
Language English
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elsevier_sciencedirect_doi_10_1016_j_ecoenv_2015_07_023
PublicationCentury 2000
PublicationDate December 2015
2015-Dec
2015-12-00
20151201
PublicationDateYYYYMMDD 2015-12-01
PublicationDate_xml – month: 12
  year: 2015
  text: December 2015
PublicationDecade 2010
PublicationPlace Netherlands
PublicationPlace_xml – name: Netherlands
PublicationTitle Ecotoxicology and environmental safety
PublicationTitleAlternate Ecotoxicol Environ Saf
PublicationYear 2015
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
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Snippet The effects of benzo(a)pyrene (BaP), dichlorodiphenyltrichloroethane (DDT) and tributyltin (TBT) association were investigated through a multi-biomarker...
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SubjectTerms Acetylcholinesterase - metabolism
Activation
Alanine Transaminase - blood
Aminolevulinic Acid - metabolism
Animals
Aspartate Aminotransferases - blood
Benzo(a)pyrene - toxicity
Biomarker
Brain - drug effects
Brain - metabolism
Catfishes - blood
Catfishes - metabolism
Contaminants
DDT
DDT - toxicity
Enzymes
Exposure
Fish
Glutathione - metabolism
Glutathione Peroxidase - metabolism
Glutathione Transferase - metabolism
Histopathology
Liver - drug effects
Liver - metabolism
Liver - pathology
Mixture
Muscles - drug effects
Muscles - metabolism
Neotropical fish
Organic pollutant
Rhamdia quelen
Toxic
Toxicity
Toxicology
Trialkyltin Compounds - toxicity
Water Pollutants, Chemical - toxicity
Title Mixtures of benzo(a)pyrene, dichlorodiphenyltrichloroethane and tributyltin are more toxic to neotropical fish Rhamdia quelen than isolated exposures
URI https://dx.doi.org/10.1016/j.ecoenv.2015.07.023
https://www.ncbi.nlm.nih.gov/pubmed/26226094
https://search.proquest.com/docview/1732836103
https://search.proquest.com/docview/1770334475
Volume 122
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