Hepatic, renal, and pancreatic damage associated with chronic exposure to oral and inhaled 2,4-dichlorophenoxy acetic acid (2,4-d): an environmental exposure model in rats
2,4-Diclophenoxyacetic acid (2,4-D) is one of the most widely used herbicides in the world. The aim of this study was to evaluate the possible toxic effect of chronic exposure to oral and inhaled 2,4-D herbicide on the liver, kidney, and pancreas by simulating environmental exposure. Eighty male alb...
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Veröffentlicht in: | Comparative clinical pathology 2020-10, Vol.29 (5), p.1001-1010 |
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description | 2,4-Diclophenoxyacetic acid (2,4-D) is one of the most widely used herbicides in the world. The aim of this study was to evaluate the possible toxic effect of chronic exposure to oral and inhaled 2,4-D herbicide on the liver, kidney, and pancreas by simulating environmental exposure. Eighty male albino adult Wistar rats divided into eight groups were exposed for 6 months to inhaled and oral (contaminated feed) three different doses of 2,4-D [3.71 × 10
−3
g of active ingredient per hectare (g a.i./ha), 6.19 × 10
−3
g a.i./ha and 9.28 × 10
−3
g a.i./ha]. Blood, liver, kidney, spleen, and pancreas samples were collected for analysis. There was a difference in ALT (alanine aminotransferase) levels between groups exposed to 2,4-D. The groups exposed to oral 2,4-D had a higher incidence of steatosis, and exposed to high doses had increased liver inflammation. All animals in the groups exposed to high 2,4-D concentrations showed renal tubular hydropic degeneration. Atrophy of Langerhans islets was observed in animals exposed to 2,4-D. The simulation of chronic environmental exposure to the 2,4-D herbicide resulted in hepatic changes that were both dose-dependent and exposure-dependent and renal and pancreatic changes that were dose-dependent. |
doi_str_mv | 10.1007/s00580-020-03150-8 |
format | Article |
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−3
g of active ingredient per hectare (g a.i./ha), 6.19 × 10
−3
g a.i./ha and 9.28 × 10
−3
g a.i./ha]. Blood, liver, kidney, spleen, and pancreas samples were collected for analysis. There was a difference in ALT (alanine aminotransferase) levels between groups exposed to 2,4-D. The groups exposed to oral 2,4-D had a higher incidence of steatosis, and exposed to high doses had increased liver inflammation. All animals in the groups exposed to high 2,4-D concentrations showed renal tubular hydropic degeneration. Atrophy of Langerhans islets was observed in animals exposed to 2,4-D. The simulation of chronic environmental exposure to the 2,4-D herbicide resulted in hepatic changes that were both dose-dependent and exposure-dependent and renal and pancreatic changes that were dose-dependent.</description><identifier>ISSN: 1618-5641</identifier><identifier>EISSN: 1618-565X</identifier><identifier>DOI: 10.1007/s00580-020-03150-8</identifier><language>eng</language><publisher>London: Springer London</publisher><subject>2,4-D ; Acetic acid ; Alanine ; Alanine transaminase ; Animal models ; Atrophy ; Chronic exposure ; Degeneration ; Hematology ; Herbicides ; Kidneys ; Liver ; Medicine ; Medicine & Public Health ; Oncology ; Original Article ; Pancreas ; Pathology ; Spleen ; Steatosis</subject><ispartof>Comparative clinical pathology, 2020-10, Vol.29 (5), p.1001-1010</ispartof><rights>Springer-Verlag London Ltd., part of Springer Nature 2020</rights><rights>Springer-Verlag London Ltd., part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2348-92e8149412270e0fa182d7c99dc53cd2d77b9ad7f3ad07a62b4a20bfef4c36413</citedby><cites>FETCH-LOGICAL-c2348-92e8149412270e0fa182d7c99dc53cd2d77b9ad7f3ad07a62b4a20bfef4c36413</cites><orcidid>0000-0001-9115-0925 ; 0000-0001-8238-8325 ; 0000-0002-5228-5488 ; 0000-0001-5202-6446 ; 0000-0003-1674-7371 ; 0000-0003-2612-4434</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00580-020-03150-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00580-020-03150-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Bonfim, Daniel José Pimentel</creatorcontrib><creatorcontrib>Magalhães, Letícia Rocha</creatorcontrib><creatorcontrib>Chagas, Pedro Henrique Nahas</creatorcontrib><creatorcontrib>Serra, Fernanda de Maria</creatorcontrib><creatorcontrib>Benatti, Liliane Aparecida Tanus</creatorcontrib><creatorcontrib>Nai, Gisele Alborghetti</creatorcontrib><title>Hepatic, renal, and pancreatic damage associated with chronic exposure to oral and inhaled 2,4-dichlorophenoxy acetic acid (2,4-d): an environmental exposure model in rats</title><title>Comparative clinical pathology</title><addtitle>Comp Clin Pathol</addtitle><description>2,4-Diclophenoxyacetic acid (2,4-D) is one of the most widely used herbicides in the world. The aim of this study was to evaluate the possible toxic effect of chronic exposure to oral and inhaled 2,4-D herbicide on the liver, kidney, and pancreas by simulating environmental exposure. Eighty male albino adult Wistar rats divided into eight groups were exposed for 6 months to inhaled and oral (contaminated feed) three different doses of 2,4-D [3.71 × 10
−3
g of active ingredient per hectare (g a.i./ha), 6.19 × 10
−3
g a.i./ha and 9.28 × 10
−3
g a.i./ha]. Blood, liver, kidney, spleen, and pancreas samples were collected for analysis. There was a difference in ALT (alanine aminotransferase) levels between groups exposed to 2,4-D. The groups exposed to oral 2,4-D had a higher incidence of steatosis, and exposed to high doses had increased liver inflammation. All animals in the groups exposed to high 2,4-D concentrations showed renal tubular hydropic degeneration. Atrophy of Langerhans islets was observed in animals exposed to 2,4-D. The simulation of chronic environmental exposure to the 2,4-D herbicide resulted in hepatic changes that were both dose-dependent and exposure-dependent and renal and pancreatic changes that were dose-dependent.</description><subject>2,4-D</subject><subject>Acetic acid</subject><subject>Alanine</subject><subject>Alanine transaminase</subject><subject>Animal models</subject><subject>Atrophy</subject><subject>Chronic exposure</subject><subject>Degeneration</subject><subject>Hematology</subject><subject>Herbicides</subject><subject>Kidneys</subject><subject>Liver</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Pancreas</subject><subject>Pathology</subject><subject>Spleen</subject><subject>Steatosis</subject><issn>1618-5641</issn><issn>1618-565X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kctOwzAQRSMEEuXxA6wssQGpAb_SJOxQxUtCYgMSO2tqT5pUiR3slMc38ZO4LSo7FqMZ2feexb1JcsLoBaM0vwyUZgVNKY8jWEbTYicZsQkr0mySve5ub8n2k4MQFpSyrBBilHzfYw9Do8fEo4V2TMAa0oPVHlfPxEAHcyQQgtMNDGjIRzPURNfe2fiNn70LS49kcMR5aNf2xtbQRiUfy9Q0um6dd32N1n1-EdC4woJuDDlbC86voomgfW8iskM7RMoW2zmDbQQSD0M4SvYqaAMe_-7D5OX25nl6nz4-3T1Mrx9TzYUs0pJjwWQpGec5RVoBK7jJdVkanQlt4p3PSjB5JcDQHCZ8JoHTWYWV1CImJA6T0w239-5tiWFQC7f0MZ2guJQ85sZ5GVV8o9LeheCxUr1vOvBfilG1KkVtSlGxFLUuRRXRJDamEMV2jv4P_Y_rB8XmkNA</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Bonfim, Daniel José Pimentel</creator><creator>Magalhães, Letícia Rocha</creator><creator>Chagas, Pedro Henrique Nahas</creator><creator>Serra, Fernanda de Maria</creator><creator>Benatti, Liliane Aparecida Tanus</creator><creator>Nai, Gisele Alborghetti</creator><general>Springer London</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0001-9115-0925</orcidid><orcidid>https://orcid.org/0000-0001-8238-8325</orcidid><orcidid>https://orcid.org/0000-0002-5228-5488</orcidid><orcidid>https://orcid.org/0000-0001-5202-6446</orcidid><orcidid>https://orcid.org/0000-0003-1674-7371</orcidid><orcidid>https://orcid.org/0000-0003-2612-4434</orcidid></search><sort><creationdate>20201001</creationdate><title>Hepatic, renal, and pancreatic damage associated with chronic exposure to oral and inhaled 2,4-dichlorophenoxy acetic acid (2,4-d): an environmental exposure model in rats</title><author>Bonfim, Daniel José Pimentel ; Magalhães, Letícia Rocha ; Chagas, Pedro Henrique Nahas ; Serra, Fernanda de Maria ; Benatti, Liliane Aparecida Tanus ; Nai, Gisele Alborghetti</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2348-92e8149412270e0fa182d7c99dc53cd2d77b9ad7f3ad07a62b4a20bfef4c36413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>2,4-D</topic><topic>Acetic acid</topic><topic>Alanine</topic><topic>Alanine transaminase</topic><topic>Animal models</topic><topic>Atrophy</topic><topic>Chronic exposure</topic><topic>Degeneration</topic><topic>Hematology</topic><topic>Herbicides</topic><topic>Kidneys</topic><topic>Liver</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Pancreas</topic><topic>Pathology</topic><topic>Spleen</topic><topic>Steatosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonfim, Daniel José Pimentel</creatorcontrib><creatorcontrib>Magalhães, Letícia Rocha</creatorcontrib><creatorcontrib>Chagas, Pedro Henrique Nahas</creatorcontrib><creatorcontrib>Serra, Fernanda de Maria</creatorcontrib><creatorcontrib>Benatti, Liliane Aparecida Tanus</creatorcontrib><creatorcontrib>Nai, Gisele Alborghetti</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Comparative clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bonfim, Daniel José Pimentel</au><au>Magalhães, Letícia Rocha</au><au>Chagas, Pedro Henrique Nahas</au><au>Serra, Fernanda de Maria</au><au>Benatti, Liliane Aparecida Tanus</au><au>Nai, Gisele Alborghetti</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatic, renal, and pancreatic damage associated with chronic exposure to oral and inhaled 2,4-dichlorophenoxy acetic acid (2,4-d): an environmental exposure model in rats</atitle><jtitle>Comparative clinical pathology</jtitle><stitle>Comp Clin Pathol</stitle><date>2020-10-01</date><risdate>2020</risdate><volume>29</volume><issue>5</issue><spage>1001</spage><epage>1010</epage><pages>1001-1010</pages><issn>1618-5641</issn><eissn>1618-565X</eissn><abstract>2,4-Diclophenoxyacetic acid (2,4-D) is one of the most widely used herbicides in the world. The aim of this study was to evaluate the possible toxic effect of chronic exposure to oral and inhaled 2,4-D herbicide on the liver, kidney, and pancreas by simulating environmental exposure. Eighty male albino adult Wistar rats divided into eight groups were exposed for 6 months to inhaled and oral (contaminated feed) three different doses of 2,4-D [3.71 × 10
−3
g of active ingredient per hectare (g a.i./ha), 6.19 × 10
−3
g a.i./ha and 9.28 × 10
−3
g a.i./ha]. Blood, liver, kidney, spleen, and pancreas samples were collected for analysis. There was a difference in ALT (alanine aminotransferase) levels between groups exposed to 2,4-D. The groups exposed to oral 2,4-D had a higher incidence of steatosis, and exposed to high doses had increased liver inflammation. All animals in the groups exposed to high 2,4-D concentrations showed renal tubular hydropic degeneration. Atrophy of Langerhans islets was observed in animals exposed to 2,4-D. The simulation of chronic environmental exposure to the 2,4-D herbicide resulted in hepatic changes that were both dose-dependent and exposure-dependent and renal and pancreatic changes that were dose-dependent.</abstract><cop>London</cop><pub>Springer London</pub><doi>10.1007/s00580-020-03150-8</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-9115-0925</orcidid><orcidid>https://orcid.org/0000-0001-8238-8325</orcidid><orcidid>https://orcid.org/0000-0002-5228-5488</orcidid><orcidid>https://orcid.org/0000-0001-5202-6446</orcidid><orcidid>https://orcid.org/0000-0003-1674-7371</orcidid><orcidid>https://orcid.org/0000-0003-2612-4434</orcidid></addata></record> |
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subjects | 2,4-D Acetic acid Alanine Alanine transaminase Animal models Atrophy Chronic exposure Degeneration Hematology Herbicides Kidneys Liver Medicine Medicine & Public Health Oncology Original Article Pancreas Pathology Spleen Steatosis |
title | Hepatic, renal, and pancreatic damage associated with chronic exposure to oral and inhaled 2,4-dichlorophenoxy acetic acid (2,4-d): an environmental exposure model in rats |
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