Learning deficits expressed as delayed extinction of a conditioned running response following perinatal exposure to vinclozolin
Vinclozolin (Vz) is one member of a group of fungicides whose metabolites are androgen receptor antagonists. These fungicides have been shown to block androgen-driven development and compromise reproductive function. The current study sought to determine if Vz also affects learning following exposur...
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Veröffentlicht in: | Neurotoxicology and teratology 2006-07, Vol.28 (4), p.482-488 |
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description | Vinclozolin (Vz) is one member of a group of fungicides whose metabolites are androgen receptor antagonists. These fungicides have been shown to block androgen-driven development and compromise reproductive function. The current study sought to determine if Vz also affects learning following exposure to low doses during the perinatal period. To test this, an androgen-dependent behavior was examined, the extinction of a previously reinforced running response. Pregnant Long–Evans rats were administered a daily oral dose of 0, 1.5, 3, 6 or 12 mg/kg Vz from the 14th day of gestation through postnatal day 3. After reaching adulthood, male and female offspring were trained to run through a short alleyway for food reinforcement. Acquisition of the response was not affected by Vz exposure. However, males required more trials than females for response extinction once food was no longer available in the apparatus. Males exposed to 6 or 12 mg/kg Vz failed to show any extinction by the end of the procedure, while the lowest dose of Vz appeared to facilitate extinction in both male and female offspring. These results demonstrate that endocrine disrupting antiandrogens can alter nervous system development in addition to the reproductive system. |
doi_str_mv | 10.1016/j.ntt.2006.04.002 |
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These fungicides have been shown to block androgen-driven development and compromise reproductive function. The current study sought to determine if Vz also affects learning following exposure to low doses during the perinatal period. To test this, an androgen-dependent behavior was examined, the extinction of a previously reinforced running response. Pregnant Long–Evans rats were administered a daily oral dose of 0, 1.5, 3, 6 or 12 mg/kg Vz from the 14th day of gestation through postnatal day 3. After reaching adulthood, male and female offspring were trained to run through a short alleyway for food reinforcement. Acquisition of the response was not affected by Vz exposure. However, males required more trials than females for response extinction once food was no longer available in the apparatus. Males exposed to 6 or 12 mg/kg Vz failed to show any extinction by the end of the procedure, while the lowest dose of Vz appeared to facilitate extinction in both male and female offspring. 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These fungicides have been shown to block androgen-driven development and compromise reproductive function. The current study sought to determine if Vz also affects learning following exposure to low doses during the perinatal period. To test this, an androgen-dependent behavior was examined, the extinction of a previously reinforced running response. Pregnant Long–Evans rats were administered a daily oral dose of 0, 1.5, 3, 6 or 12 mg/kg Vz from the 14th day of gestation through postnatal day 3. After reaching adulthood, male and female offspring were trained to run through a short alleyway for food reinforcement. Acquisition of the response was not affected by Vz exposure. However, males required more trials than females for response extinction once food was no longer available in the apparatus. Males exposed to 6 or 12 mg/kg Vz failed to show any extinction by the end of the procedure, while the lowest dose of Vz appeared to facilitate extinction in both male and female offspring. These results demonstrate that endocrine disrupting antiandrogens can alter nervous system development in addition to the reproductive system.</description><subject>Androgen Antagonists - toxicity</subject><subject>Animals</subject><subject>Antiandrogen</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Conditioning, Operant - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Extinction, Psychological - drug effects</subject><subject>Female</subject><subject>Feminization - chemically induced</subject><subject>Fungicides, Industrial - toxicity</subject><subject>Learning</subject><subject>Learning Disorders - chemically induced</subject><subject>Learning Disorders - psychology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Operant behavior</subject><subject>Oxazoles - toxicity</subject><subject>Penis - drug effects</subject><subject>Perinatal exposure</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Reflex - drug effects</subject><subject>Reproduction - drug effects</subject><subject>Running - psychology</subject><subject>Sex Characteristics</subject><subject>Toxicology</subject><subject>Vinclozolin</subject><issn>0892-0362</issn><issn>1872-9738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFvFCEUxonR2G31D_Bi5mJvMwWGYZh4Mk1rTTbxomfCwsOwYWEEprZe_NfLuJv0pifg8fu-vPc-hN4R3BFM-NW-C6V0FGPeYdZhTF-gDREjbaexFy_RBouJtrjn9Ayd57zHGI-c4NfojPCRD5gOG_RnCyoFF340BqzTruQGHuYEOYNpVK5Vrx7rFR6KC7q4GJpoG9XoGIxbn_UvLeGvQ1XNMWRobPQ-_lpLMyQXVFF-dY15SdCU2NxXKx9_R-_CG_TKKp_h7em8QN9vb75d37Xbr5-_XH_atpqxvrQjNZYpIDsyccPGfhJWccqp4RprBcYaY6lmSpmdNb2iPR0FryMOAxsGxXb9Bbo8-s4p_lwgF3lwWYP3KkBcsiRTLwYy8P-DTGDMJlFBcgR1ijknsHJO7qDSoyRYrvHIvazxyDUeiZms8VTN-5P5sjuAeVac8qjAhxOgslbeJhW0y8-cIIyLnlTu45GDurN7B0lm7SBoMC6BLtJE9482ngDkfbEq</recordid><startdate>20060701</startdate><enddate>20060701</enddate><creator>André, Susan M.</creator><creator>Markowski, Vincent P.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><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>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7TK</scope><scope>7U7</scope></search><sort><creationdate>20060701</creationdate><title>Learning deficits expressed as delayed extinction of a conditioned running response following perinatal exposure to vinclozolin</title><author>André, Susan M. ; Markowski, Vincent P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-72df4ae1b196d47398fa6262d6c0caedfddf2c4aadbfd3a23278665055455a4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Androgen Antagonists - toxicity</topic><topic>Animals</topic><topic>Antiandrogen</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Conditioning, Operant - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Extinction, Psychological - drug effects</topic><topic>Female</topic><topic>Feminization - chemically induced</topic><topic>Fungicides, Industrial - toxicity</topic><topic>Learning</topic><topic>Learning Disorders - chemically induced</topic><topic>Learning Disorders - psychology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Operant behavior</topic><topic>Oxazoles - toxicity</topic><topic>Penis - drug effects</topic><topic>Perinatal exposure</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Long-Evans</topic><topic>Reflex - drug effects</topic><topic>Reproduction - drug effects</topic><topic>Running - psychology</topic><topic>Sex Characteristics</topic><topic>Toxicology</topic><topic>Vinclozolin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>André, Susan M.</creatorcontrib><creatorcontrib>Markowski, Vincent P.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><jtitle>Neurotoxicology and teratology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>André, Susan M.</au><au>Markowski, Vincent P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Learning deficits expressed as delayed extinction of a conditioned running response following perinatal exposure to vinclozolin</atitle><jtitle>Neurotoxicology and teratology</jtitle><addtitle>Neurotoxicol Teratol</addtitle><date>2006-07-01</date><risdate>2006</risdate><volume>28</volume><issue>4</issue><spage>482</spage><epage>488</epage><pages>482-488</pages><issn>0892-0362</issn><eissn>1872-9738</eissn><coden>NETEEC</coden><abstract>Vinclozolin (Vz) is one member of a group of fungicides whose metabolites are androgen receptor antagonists. These fungicides have been shown to block androgen-driven development and compromise reproductive function. The current study sought to determine if Vz also affects learning following exposure to low doses during the perinatal period. To test this, an androgen-dependent behavior was examined, the extinction of a previously reinforced running response. Pregnant Long–Evans rats were administered a daily oral dose of 0, 1.5, 3, 6 or 12 mg/kg Vz from the 14th day of gestation through postnatal day 3. After reaching adulthood, male and female offspring were trained to run through a short alleyway for food reinforcement. Acquisition of the response was not affected by Vz exposure. However, males required more trials than females for response extinction once food was no longer available in the apparatus. Males exposed to 6 or 12 mg/kg Vz failed to show any extinction by the end of the procedure, while the lowest dose of Vz appeared to facilitate extinction in both male and female offspring. These results demonstrate that endocrine disrupting antiandrogens can alter nervous system development in addition to the reproductive system.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>16765025</pmid><doi>10.1016/j.ntt.2006.04.002</doi><tpages>7</tpages></addata></record> |
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subjects | Androgen Antagonists - toxicity Animals Antiandrogen Biological and medical sciences Body Weight - drug effects Conditioning, Operant - drug effects Dose-Response Relationship, Drug Extinction, Psychological - drug effects Female Feminization - chemically induced Fungicides, Industrial - toxicity Learning Learning Disorders - chemically induced Learning Disorders - psychology Male Medical sciences Operant behavior Oxazoles - toxicity Penis - drug effects Perinatal exposure Rat Rats Rats, Long-Evans Reflex - drug effects Reproduction - drug effects Running - psychology Sex Characteristics Toxicology Vinclozolin |
title | Learning deficits expressed as delayed extinction of a conditioned running response following perinatal exposure to vinclozolin |
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