Perfluorooctane sulfonate (PFOS) exposure could modify the dopaminergic system in several limbic brain regions
•Dopamine concentration and metabolism are modified by PFOS in some limbic regions.•PFOS affects D1 and D2 receptors in amygdala, prefrontal cortex and hippocampus.•The above alterations could be a possible mechanism of PFOS neurotoxicity. Perfluorooctane sulfonate (PFOS) is the most representative...
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Veröffentlicht in: | Toxicology letters 2016-01, Vol.240 (1), p.226-235 |
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description | •Dopamine concentration and metabolism are modified by PFOS in some limbic regions.•PFOS affects D1 and D2 receptors in amygdala, prefrontal cortex and hippocampus.•The above alterations could be a possible mechanism of PFOS neurotoxicity.
Perfluorooctane sulfonate (PFOS) is the most representative of a rising class of persistent organic pollutants perfluorochemicals. In the present study, its neurotoxicity was examined using adult male rats orally treated with 0.5; 1.0; 3.0 and 6.0mg of PFOS/kg/day for 28 days. At the end of the treatment, the dopamine concentration and its metabolism expressed like the ratio 3,4-dihydroxyphenylacetic acid (DOPAC)/dopamine and homovanillic acid (HVA)/dopamine were measured in the amygdala, prefrontal cortex and hippocampus. Gene and protein expression of the dopamine receptors D1 and D2 were also determined in these limbic areas. The obtained results suggest that: (1) PFOS can alter the dopamine system by modifying its neuronal activity and/or its D1 and D2 receptors in the studied brain regions; (2) the dopamine concentration and metabolism seem to be more sensitive against PFOS toxicity in the hippocampus than in the other analyzed brain areas; (3) the inhibited gene and protein expression of the D1 receptors induced by PFOS in the amygdala could be related to several changes in the HPA axis activity, and lastly; (4) the observed alterations on the dopamine system induced by PFOS could be a possible neurotoxicity mechanism of PFOS, leading to many neurological diseases. |
doi_str_mv | 10.1016/j.toxlet.2015.10.023 |
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Perfluorooctane sulfonate (PFOS) is the most representative of a rising class of persistent organic pollutants perfluorochemicals. In the present study, its neurotoxicity was examined using adult male rats orally treated with 0.5; 1.0; 3.0 and 6.0mg of PFOS/kg/day for 28 days. At the end of the treatment, the dopamine concentration and its metabolism expressed like the ratio 3,4-dihydroxyphenylacetic acid (DOPAC)/dopamine and homovanillic acid (HVA)/dopamine were measured in the amygdala, prefrontal cortex and hippocampus. Gene and protein expression of the dopamine receptors D1 and D2 were also determined in these limbic areas. The obtained results suggest that: (1) PFOS can alter the dopamine system by modifying its neuronal activity and/or its D1 and D2 receptors in the studied brain regions; (2) the dopamine concentration and metabolism seem to be more sensitive against PFOS toxicity in the hippocampus than in the other analyzed brain areas; (3) the inhibited gene and protein expression of the D1 receptors induced by PFOS in the amygdala could be related to several changes in the HPA axis activity, and lastly; (4) the observed alterations on the dopamine system induced by PFOS could be a possible neurotoxicity mechanism of PFOS, leading to many neurological diseases.</description><identifier>ISSN: 0378-4274</identifier><identifier>EISSN: 1879-3169</identifier><identifier>DOI: 10.1016/j.toxlet.2015.10.023</identifier><identifier>PMID: 26529483</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>3,4-Dihydroxyphenylacetic Acid - metabolism ; Alkanesulfonic Acids - toxicity ; Amygdala ; Amygdala - drug effects ; Amygdala - metabolism ; Animals ; Brain ; Dopamine ; Dose-Response Relationship, Drug ; Fluorocarbons - toxicity ; Gene expression ; Genes ; Hippocampus ; Hippocampus - drug effects ; Hippocampus - metabolism ; Homovanillic Acid - metabolism ; Hypothalamo-Hypophyseal System - drug effects ; Hypothalamo-Hypophyseal System - metabolism ; Limbic system ; Male ; Metabolism ; PFOS ; Prefrontal cortex ; Prefrontal Cortex - drug effects ; Prefrontal Cortex - metabolism ; Rat ; Rats ; Rats, Sprague-Dawley ; Receptors ; Receptors, Dopamine D1 - metabolism ; Receptors, Dopamine D2 - metabolism ; Sulfonates</subject><ispartof>Toxicology letters, 2016-01, Vol.240 (1), p.226-235</ispartof><rights>2015 Elsevier Ireland Ltd</rights><rights>Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-17e16551e31ea3b8daeab9367a56842aa36eddeede00e3bca5fd962f87b1b2213</citedby><cites>FETCH-LOGICAL-c428t-17e16551e31ea3b8daeab9367a56842aa36eddeede00e3bca5fd962f87b1b2213</cites><orcidid>0000-0002-2123-6974</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0378427415300886$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26529483$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Salgado, R.</creatorcontrib><creatorcontrib>López-Doval, S.</creatorcontrib><creatorcontrib>Pereiro, N.</creatorcontrib><creatorcontrib>Lafuente, A.</creatorcontrib><title>Perfluorooctane sulfonate (PFOS) exposure could modify the dopaminergic system in several limbic brain regions</title><title>Toxicology letters</title><addtitle>Toxicol Lett</addtitle><description>•Dopamine concentration and metabolism are modified by PFOS in some limbic regions.•PFOS affects D1 and D2 receptors in amygdala, prefrontal cortex and hippocampus.•The above alterations could be a possible mechanism of PFOS neurotoxicity.
Perfluorooctane sulfonate (PFOS) is the most representative of a rising class of persistent organic pollutants perfluorochemicals. In the present study, its neurotoxicity was examined using adult male rats orally treated with 0.5; 1.0; 3.0 and 6.0mg of PFOS/kg/day for 28 days. At the end of the treatment, the dopamine concentration and its metabolism expressed like the ratio 3,4-dihydroxyphenylacetic acid (DOPAC)/dopamine and homovanillic acid (HVA)/dopamine were measured in the amygdala, prefrontal cortex and hippocampus. Gene and protein expression of the dopamine receptors D1 and D2 were also determined in these limbic areas. The obtained results suggest that: (1) PFOS can alter the dopamine system by modifying its neuronal activity and/or its D1 and D2 receptors in the studied brain regions; (2) the dopamine concentration and metabolism seem to be more sensitive against PFOS toxicity in the hippocampus than in the other analyzed brain areas; (3) the inhibited gene and protein expression of the D1 receptors induced by PFOS in the amygdala could be related to several changes in the HPA axis activity, and lastly; (4) the observed alterations on the dopamine system induced by PFOS could be a possible neurotoxicity mechanism of PFOS, leading to many neurological diseases.</description><subject>3,4-Dihydroxyphenylacetic Acid - metabolism</subject><subject>Alkanesulfonic Acids - toxicity</subject><subject>Amygdala</subject><subject>Amygdala - drug effects</subject><subject>Amygdala - metabolism</subject><subject>Animals</subject><subject>Brain</subject><subject>Dopamine</subject><subject>Dose-Response Relationship, Drug</subject><subject>Fluorocarbons - toxicity</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Homovanillic Acid - metabolism</subject><subject>Hypothalamo-Hypophyseal System - drug effects</subject><subject>Hypothalamo-Hypophyseal System - metabolism</subject><subject>Limbic system</subject><subject>Male</subject><subject>Metabolism</subject><subject>PFOS</subject><subject>Prefrontal cortex</subject><subject>Prefrontal Cortex - drug effects</subject><subject>Prefrontal Cortex - metabolism</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors</subject><subject>Receptors, Dopamine D1 - metabolism</subject><subject>Receptors, Dopamine D2 - metabolism</subject><subject>Sulfonates</subject><issn>0378-4274</issn><issn>1879-3169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1r3DAQhkVoabZJ_0EoOiYHb_VhSfYlUELSFgIJtDkLWRqnWmRrI8kh---jZdMeS0-CV8_MMPMgdEbJmhIqv2zWJb4EKGtGqKjRmjB-hFa0U33DqezfoRXhqmtaptpj9DHnDSFEtlJ8QMdMCta3HV-h-R7SGJaYYrTFzIDzEsY4mwL4_P7m7ucFhpdtzEsCbOMSHJ6i8-MOl9-AXdyayc-QHr3FeZcLTNjPOMMzJBNw8NNQP4Zkapjg0cc5n6L3owkZPr29J-jh5vrX1ffm9u7bj6uvt41tWVcaqoBKIShwCoYPnTNghp5LZYTsWmYMl-AcgANCgA_WiNH1ko2dGujAGOUn6PzQd5vi0wK56MlnCyHUFeOSNVWqI1zQtv8PVFBGGRGqou0BtSnmnGDU2-Qnk3aaEr2Xojf6IEXvpezTKqWWfX6bsAwTuL9FfyxU4PIAQD3Js4eks_UwW3A-gS3aRf_vCa8d1KG5</recordid><startdate>20160105</startdate><enddate>20160105</enddate><creator>Salgado, R.</creator><creator>López-Doval, S.</creator><creator>Pereiro, N.</creator><creator>Lafuente, A.</creator><general>Elsevier B.V</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>7TV</scope><scope>7U7</scope><scope>C1K</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope><orcidid>https://orcid.org/0000-0002-2123-6974</orcidid></search><sort><creationdate>20160105</creationdate><title>Perfluorooctane sulfonate (PFOS) exposure could modify the dopaminergic system in several limbic brain regions</title><author>Salgado, R. ; López-Doval, S. ; Pereiro, N. ; Lafuente, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-17e16551e31ea3b8daeab9367a56842aa36eddeede00e3bca5fd962f87b1b2213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>3,4-Dihydroxyphenylacetic Acid - metabolism</topic><topic>Alkanesulfonic Acids - toxicity</topic><topic>Amygdala</topic><topic>Amygdala - drug effects</topic><topic>Amygdala - metabolism</topic><topic>Animals</topic><topic>Brain</topic><topic>Dopamine</topic><topic>Dose-Response Relationship, Drug</topic><topic>Fluorocarbons - toxicity</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Hippocampus</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Homovanillic Acid - metabolism</topic><topic>Hypothalamo-Hypophyseal System - drug effects</topic><topic>Hypothalamo-Hypophyseal System - metabolism</topic><topic>Limbic system</topic><topic>Male</topic><topic>Metabolism</topic><topic>PFOS</topic><topic>Prefrontal cortex</topic><topic>Prefrontal Cortex - drug effects</topic><topic>Prefrontal Cortex - metabolism</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors</topic><topic>Receptors, Dopamine D1 - metabolism</topic><topic>Receptors, Dopamine D2 - metabolism</topic><topic>Sulfonates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salgado, R.</creatorcontrib><creatorcontrib>López-Doval, S.</creatorcontrib><creatorcontrib>Pereiro, N.</creatorcontrib><creatorcontrib>Lafuente, A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pollution Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Toxicology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salgado, R.</au><au>López-Doval, S.</au><au>Pereiro, N.</au><au>Lafuente, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Perfluorooctane sulfonate (PFOS) exposure could modify the dopaminergic system in several limbic brain regions</atitle><jtitle>Toxicology letters</jtitle><addtitle>Toxicol Lett</addtitle><date>2016-01-05</date><risdate>2016</risdate><volume>240</volume><issue>1</issue><spage>226</spage><epage>235</epage><pages>226-235</pages><issn>0378-4274</issn><eissn>1879-3169</eissn><abstract>•Dopamine concentration and metabolism are modified by PFOS in some limbic regions.•PFOS affects D1 and D2 receptors in amygdala, prefrontal cortex and hippocampus.•The above alterations could be a possible mechanism of PFOS neurotoxicity.
Perfluorooctane sulfonate (PFOS) is the most representative of a rising class of persistent organic pollutants perfluorochemicals. In the present study, its neurotoxicity was examined using adult male rats orally treated with 0.5; 1.0; 3.0 and 6.0mg of PFOS/kg/day for 28 days. At the end of the treatment, the dopamine concentration and its metabolism expressed like the ratio 3,4-dihydroxyphenylacetic acid (DOPAC)/dopamine and homovanillic acid (HVA)/dopamine were measured in the amygdala, prefrontal cortex and hippocampus. Gene and protein expression of the dopamine receptors D1 and D2 were also determined in these limbic areas. The obtained results suggest that: (1) PFOS can alter the dopamine system by modifying its neuronal activity and/or its D1 and D2 receptors in the studied brain regions; (2) the dopamine concentration and metabolism seem to be more sensitive against PFOS toxicity in the hippocampus than in the other analyzed brain areas; (3) the inhibited gene and protein expression of the D1 receptors induced by PFOS in the amygdala could be related to several changes in the HPA axis activity, and lastly; (4) the observed alterations on the dopamine system induced by PFOS could be a possible neurotoxicity mechanism of PFOS, leading to many neurological diseases.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26529483</pmid><doi>10.1016/j.toxlet.2015.10.023</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2123-6974</orcidid></addata></record> |
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subjects | 3,4-Dihydroxyphenylacetic Acid - metabolism Alkanesulfonic Acids - toxicity Amygdala Amygdala - drug effects Amygdala - metabolism Animals Brain Dopamine Dose-Response Relationship, Drug Fluorocarbons - toxicity Gene expression Genes Hippocampus Hippocampus - drug effects Hippocampus - metabolism Homovanillic Acid - metabolism Hypothalamo-Hypophyseal System - drug effects Hypothalamo-Hypophyseal System - metabolism Limbic system Male Metabolism PFOS Prefrontal cortex Prefrontal Cortex - drug effects Prefrontal Cortex - metabolism Rat Rats Rats, Sprague-Dawley Receptors Receptors, Dopamine D1 - metabolism Receptors, Dopamine D2 - metabolism Sulfonates |
title | Perfluorooctane sulfonate (PFOS) exposure could modify the dopaminergic system in several limbic brain regions |
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