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Effect of maternal lipopolysaccharide administration on the development of dopaminergic receptors and transporter in the rat offspring
Epidemiological evidence supports that maternal infection during gestation are notable risk factors for developmental mental illnesses including schizophrenia and autism. In prenatal lipopolysaccharide (LPS) model of immune activation in rats, the offspring exhibit significant impairments in behavio...
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description | Epidemiological evidence supports that maternal infection during gestation are notable risk factors for developmental mental illnesses including schizophrenia and autism. In prenatal lipopolysaccharide (LPS) model of immune activation in rats, the offspring exhibit significant impairments in behaviors mediated by central dopamine (DA) system. This study aimed to examine the temporal and regional pattern of postnatal DA development in the male offspring of pregnant Sprague-Dawley rats administered with 100 µg/kg LPS or saline at gestational days 15/16. Using ligand autoradiography, D1 and D2 dopamine receptors (D1R, D2R) and dopamine transporter (DAT) binding levels were measured in the prefrontal cortex (PFC) and sub cortical regions (dorsal striatum and nucleus accumbens core and shell) at pre pubertal (P35) and post pubertal ages (P60). We found a significant decrease in D2R ligand [(3)H] YM-90151-2 binding in the medial PFC (mPFC) in prenatal LPS-treated animals at P35 and P60 compared to respective saline groups. The decrease in D2R levels was not observed in the striatum or accumbens of maternal LPS-treated animals. No significant changes were observed in [(3)H] SCH23390 binding to D1R. However, the level of [(125)I] RTI-121 binding to DAT was selectively reduced in the nucleus accumbens core and shell at P35 in the prenatal LPS group. Immunohistochemical analysis showed that number of D2R immunopositive cells in infralimbic/prelimbic (IL/PL) part of mPFC was significantly reduced in the LPS group at P60. Prenatal LPS treatment did not significantly affect either the total number of mature neurons or parvalbumin (PV)-immunopositive interneurons in this region. However the number of PV and D2R co-labeled neurons was significantly reduced in the IL/PL subregion of PFC of LPS treated animals. Our data suggests D2R deficit in the PFC and PV interneurons may be relevant to understanding mechanisms of cortical dysfunctions described in prenatal infection animal models as well as schizophrenia. |
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In prenatal lipopolysaccharide (LPS) model of immune activation in rats, the offspring exhibit significant impairments in behaviors mediated by central dopamine (DA) system. This study aimed to examine the temporal and regional pattern of postnatal DA development in the male offspring of pregnant Sprague-Dawley rats administered with 100 µg/kg LPS or saline at gestational days 15/16. Using ligand autoradiography, D1 and D2 dopamine receptors (D1R, D2R) and dopamine transporter (DAT) binding levels were measured in the prefrontal cortex (PFC) and sub cortical regions (dorsal striatum and nucleus accumbens core and shell) at pre pubertal (P35) and post pubertal ages (P60). We found a significant decrease in D2R ligand [(3)H] YM-90151-2 binding in the medial PFC (mPFC) in prenatal LPS-treated animals at P35 and P60 compared to respective saline groups. The decrease in D2R levels was not observed in the striatum or accumbens of maternal LPS-treated animals. No significant changes were observed in [(3)H] SCH23390 binding to D1R. However, the level of [(125)I] RTI-121 binding to DAT was selectively reduced in the nucleus accumbens core and shell at P35 in the prenatal LPS group. Immunohistochemical analysis showed that number of D2R immunopositive cells in infralimbic/prelimbic (IL/PL) part of mPFC was significantly reduced in the LPS group at P60. Prenatal LPS treatment did not significantly affect either the total number of mature neurons or parvalbumin (PV)-immunopositive interneurons in this region. However the number of PV and D2R co-labeled neurons was significantly reduced in the IL/PL subregion of PFC of LPS treated animals. Our data suggests D2R deficit in the PFC and PV interneurons may be relevant to understanding mechanisms of cortical dysfunctions described in prenatal infection animal models as well as schizophrenia.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0054439</identifier><identifier>PMID: 23349891</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acids ; Animal cognition ; Animal models ; Animals ; Autism ; Autoradiography ; Bacterial infections ; Binding ; Biology ; Brain ; Caudate-putamen ; Child development ; Cortex (temporal) ; Dopamine ; Dopamine - metabolism ; Dopamine D1 receptors ; Dopamine D2 receptors ; Dopamine Plasma Membrane Transport Proteins - metabolism ; Dopamine receptors ; Dopamine transporter ; Dopaminergic Neurons - drug effects ; Dopaminergic Neurons - metabolism ; Epidemiology ; Female ; Gene expression ; Gestation ; Health aspects ; Illnesses ; Immune response ; Infection - chemically induced ; Infection - metabolism ; Infection - pathology ; Infections ; Infectious Disease Transmission, Vertical ; Interneurons ; Ligands ; Lipopolysaccharides ; Lipopolysaccharides - toxicity ; Male ; Medicine ; Memory ; Mental disorders ; Mental health ; Mitogens ; Neostriatum ; Neurology ; Neurons ; Neurosurgery ; Nuclei ; Nucleus accumbens ; Nucleus Accumbens - drug effects ; Nucleus Accumbens - metabolism ; Nucleus Accumbens - physiopathology ; Offspring ; Parvalbumin ; Prefrontal cortex ; Prefrontal Cortex - metabolism ; Prefrontal Cortex - physiopathology ; Pregnancy ; Psychiatry ; Rats ; Rats, Sprague-Dawley ; Receptors ; Receptors, Dopamine D1 - metabolism ; Receptors, Dopamine D1 - physiology ; Receptors, Dopamine D2 - metabolism ; Receptors, Dopamine D2 - physiology ; Regional development ; Risk analysis ; Risk factors ; Rodents ; Schizophrenia ; Studies ; Synaptic Transmission - drug effects</subject><ispartof>PloS one, 2013-01, Vol.8 (1), p.e54439</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Baharnoori et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Baharnoori et al 2013 Baharnoori et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-c1ef97f2f610b25dbf4e79ed36d8b7aa2b901365cd15427111c23a0696b04c513</citedby><cites>FETCH-LOGICAL-c692t-c1ef97f2f610b25dbf4e79ed36d8b7aa2b901365cd15427111c23a0696b04c513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1327278615/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1327278615?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23349891$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Fatemi, Hossein</contributor><creatorcontrib>Baharnoori, Moogeh</creatorcontrib><creatorcontrib>Bhardwaj, Sanjeev K</creatorcontrib><creatorcontrib>Srivastava, Lalit K</creatorcontrib><title>Effect of maternal lipopolysaccharide administration on the development of dopaminergic receptors and transporter in the rat offspring</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Epidemiological evidence supports that maternal infection during gestation are notable risk factors for developmental mental illnesses including schizophrenia and autism. In prenatal lipopolysaccharide (LPS) model of immune activation in rats, the offspring exhibit significant impairments in behaviors mediated by central dopamine (DA) system. This study aimed to examine the temporal and regional pattern of postnatal DA development in the male offspring of pregnant Sprague-Dawley rats administered with 100 µg/kg LPS or saline at gestational days 15/16. Using ligand autoradiography, D1 and D2 dopamine receptors (D1R, D2R) and dopamine transporter (DAT) binding levels were measured in the prefrontal cortex (PFC) and sub cortical regions (dorsal striatum and nucleus accumbens core and shell) at pre pubertal (P35) and post pubertal ages (P60). We found a significant decrease in D2R ligand [(3)H] YM-90151-2 binding in the medial PFC (mPFC) in prenatal LPS-treated animals at P35 and P60 compared to respective saline groups. The decrease in D2R levels was not observed in the striatum or accumbens of maternal LPS-treated animals. No significant changes were observed in [(3)H] SCH23390 binding to D1R. However, the level of [(125)I] RTI-121 binding to DAT was selectively reduced in the nucleus accumbens core and shell at P35 in the prenatal LPS group. Immunohistochemical analysis showed that number of D2R immunopositive cells in infralimbic/prelimbic (IL/PL) part of mPFC was significantly reduced in the LPS group at P60. Prenatal LPS treatment did not significantly affect either the total number of mature neurons or parvalbumin (PV)-immunopositive interneurons in this region. However the number of PV and D2R co-labeled neurons was significantly reduced in the IL/PL subregion of PFC of LPS treated animals. Our data suggests D2R deficit in the PFC and PV interneurons may be relevant to understanding mechanisms of cortical dysfunctions described in prenatal infection animal models as well as schizophrenia.</description><subject>Acids</subject><subject>Animal cognition</subject><subject>Animal models</subject><subject>Animals</subject><subject>Autism</subject><subject>Autoradiography</subject><subject>Bacterial infections</subject><subject>Binding</subject><subject>Biology</subject><subject>Brain</subject><subject>Caudate-putamen</subject><subject>Child development</subject><subject>Cortex (temporal)</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>Dopamine D1 receptors</subject><subject>Dopamine D2 receptors</subject><subject>Dopamine Plasma Membrane Transport Proteins - metabolism</subject><subject>Dopamine receptors</subject><subject>Dopamine transporter</subject><subject>Dopaminergic Neurons - drug effects</subject><subject>Dopaminergic Neurons - metabolism</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gestation</subject><subject>Health aspects</subject><subject>Illnesses</subject><subject>Immune response</subject><subject>Infection - chemically induced</subject><subject>Infection - metabolism</subject><subject>Infection - pathology</subject><subject>Infections</subject><subject>Infectious Disease Transmission, Vertical</subject><subject>Interneurons</subject><subject>Ligands</subject><subject>Lipopolysaccharides</subject><subject>Lipopolysaccharides - toxicity</subject><subject>Male</subject><subject>Medicine</subject><subject>Memory</subject><subject>Mental disorders</subject><subject>Mental health</subject><subject>Mitogens</subject><subject>Neostriatum</subject><subject>Neurology</subject><subject>Neurons</subject><subject>Neurosurgery</subject><subject>Nuclei</subject><subject>Nucleus accumbens</subject><subject>Nucleus Accumbens - drug effects</subject><subject>Nucleus Accumbens - metabolism</subject><subject>Nucleus Accumbens - physiopathology</subject><subject>Offspring</subject><subject>Parvalbumin</subject><subject>Prefrontal cortex</subject><subject>Prefrontal Cortex - metabolism</subject><subject>Prefrontal Cortex - physiopathology</subject><subject>Pregnancy</subject><subject>Psychiatry</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors</subject><subject>Receptors, Dopamine D1 - metabolism</subject><subject>Receptors, Dopamine D1 - physiology</subject><subject>Receptors, Dopamine D2 - metabolism</subject><subject>Receptors, Dopamine D2 - physiology</subject><subject>Regional development</subject><subject>Risk analysis</subject><subject>Risk factors</subject><subject>Rodents</subject><subject>Schizophrenia</subject><subject>Studies</subject><subject>Synaptic Transmission - drug effects</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk2uL1DAUhoso7kX_gWhBWPDDjM2lTfNFWJZVBxYWvH0NaXLSydA2Ncks7h_wd5uZ6S5TUJAGGpLnfXN4OSfLXqFiiQhD7zdu6wfZLUc3wLIoSkoJf5KdIk7wosIFeXq0P8nOQtgkiNRV9Tw7wYRQXnN0mv2-NgZUzJ3Jexlh55h3dnSj6-6DVGotvdWQS93bwYboZbRuyNOKa8g13EHnxh6GvYF2o0wY-Naq3IOCMTofcjnoPAmHMDqfXsjtQZysksiE0duhfZE9M7IL8HL6n2ffP15_u_q8uLn9tLq6vFmoiuO4UAgMZwabChUNLnVjKDAOmlS6bpiUuOEFIlWpNCopZgghhYksKl41BVUlIufZm4Pv2LkgpgiDQAQzzOoKlYlYHQjt5Eak4nrp74WTVuwPnG-F9NGqDoTCwGpe7gugLAVqZE2K2nClgFDAyevD9Nq26UGrlJOX3cx0fjPYtWjdnSAlZZySZPB2MvDu5xZC_EfJE9XKVJUdjEtmqrdBiUvKakwxL3iiln-h0qehtyo1kbHpfCZ4NxMkJsKv2MptCGL19cv_s7c_5uzFEbsG2cV1cN1211lhDtIDqLwLwYN5TA4VYjcDD2mI3QyIaQaS7PVx6o-ih6YnfwAFagSz</recordid><startdate>20130117</startdate><enddate>20130117</enddate><creator>Baharnoori, Moogeh</creator><creator>Bhardwaj, Sanjeev K</creator><creator>Srivastava, Lalit K</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130117</creationdate><title>Effect of maternal lipopolysaccharide administration on the development of dopaminergic receptors and transporter in the rat offspring</title><author>Baharnoori, Moogeh ; Bhardwaj, Sanjeev K ; Srivastava, Lalit K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-c1ef97f2f610b25dbf4e79ed36d8b7aa2b901365cd15427111c23a0696b04c513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Acids</topic><topic>Animal cognition</topic><topic>Animal models</topic><topic>Animals</topic><topic>Autism</topic><topic>Autoradiography</topic><topic>Bacterial infections</topic><topic>Binding</topic><topic>Biology</topic><topic>Brain</topic><topic>Caudate-putamen</topic><topic>Child development</topic><topic>Cortex (temporal)</topic><topic>Dopamine</topic><topic>Dopamine - metabolism</topic><topic>Dopamine D1 receptors</topic><topic>Dopamine D2 receptors</topic><topic>Dopamine Plasma Membrane Transport Proteins - metabolism</topic><topic>Dopamine receptors</topic><topic>Dopamine transporter</topic><topic>Dopaminergic Neurons - drug effects</topic><topic>Dopaminergic Neurons - metabolism</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gestation</topic><topic>Health aspects</topic><topic>Illnesses</topic><topic>Immune response</topic><topic>Infection - chemically induced</topic><topic>Infection - metabolism</topic><topic>Infection - pathology</topic><topic>Infections</topic><topic>Infectious Disease Transmission, Vertical</topic><topic>Interneurons</topic><topic>Ligands</topic><topic>Lipopolysaccharides</topic><topic>Lipopolysaccharides - toxicity</topic><topic>Male</topic><topic>Medicine</topic><topic>Memory</topic><topic>Mental disorders</topic><topic>Mental health</topic><topic>Mitogens</topic><topic>Neostriatum</topic><topic>Neurology</topic><topic>Neurons</topic><topic>Neurosurgery</topic><topic>Nuclei</topic><topic>Nucleus accumbens</topic><topic>Nucleus Accumbens - 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Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest advanced technologies & aerospace journals</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials science collection</collection><collection>Publicly Available Content (ProQuest)</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><collection>Engineering collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baharnoori, Moogeh</au><au>Bhardwaj, Sanjeev K</au><au>Srivastava, Lalit K</au><au>Fatemi, Hossein</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of maternal lipopolysaccharide administration on the development of dopaminergic receptors and transporter in the rat offspring</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-01-17</date><risdate>2013</risdate><volume>8</volume><issue>1</issue><spage>e54439</spage><pages>e54439-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Epidemiological evidence supports that maternal infection during gestation are notable risk factors for developmental mental illnesses including schizophrenia and autism. In prenatal lipopolysaccharide (LPS) model of immune activation in rats, the offspring exhibit significant impairments in behaviors mediated by central dopamine (DA) system. This study aimed to examine the temporal and regional pattern of postnatal DA development in the male offspring of pregnant Sprague-Dawley rats administered with 100 µg/kg LPS or saline at gestational days 15/16. Using ligand autoradiography, D1 and D2 dopamine receptors (D1R, D2R) and dopamine transporter (DAT) binding levels were measured in the prefrontal cortex (PFC) and sub cortical regions (dorsal striatum and nucleus accumbens core and shell) at pre pubertal (P35) and post pubertal ages (P60). We found a significant decrease in D2R ligand [(3)H] YM-90151-2 binding in the medial PFC (mPFC) in prenatal LPS-treated animals at P35 and P60 compared to respective saline groups. The decrease in D2R levels was not observed in the striatum or accumbens of maternal LPS-treated animals. No significant changes were observed in [(3)H] SCH23390 binding to D1R. However, the level of [(125)I] RTI-121 binding to DAT was selectively reduced in the nucleus accumbens core and shell at P35 in the prenatal LPS group. Immunohistochemical analysis showed that number of D2R immunopositive cells in infralimbic/prelimbic (IL/PL) part of mPFC was significantly reduced in the LPS group at P60. Prenatal LPS treatment did not significantly affect either the total number of mature neurons or parvalbumin (PV)-immunopositive interneurons in this region. However the number of PV and D2R co-labeled neurons was significantly reduced in the IL/PL subregion of PFC of LPS treated animals. Our data suggests D2R deficit in the PFC and PV interneurons may be relevant to understanding mechanisms of cortical dysfunctions described in prenatal infection animal models as well as schizophrenia.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23349891</pmid><doi>10.1371/journal.pone.0054439</doi><tpages>e54439</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2013-01, Vol.8 (1), p.e54439 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1327278615 |
source | PubMed Central (Open Access); Publicly Available Content (ProQuest) |
subjects | Acids Animal cognition Animal models Animals Autism Autoradiography Bacterial infections Binding Biology Brain Caudate-putamen Child development Cortex (temporal) Dopamine Dopamine - metabolism Dopamine D1 receptors Dopamine D2 receptors Dopamine Plasma Membrane Transport Proteins - metabolism Dopamine receptors Dopamine transporter Dopaminergic Neurons - drug effects Dopaminergic Neurons - metabolism Epidemiology Female Gene expression Gestation Health aspects Illnesses Immune response Infection - chemically induced Infection - metabolism Infection - pathology Infections Infectious Disease Transmission, Vertical Interneurons Ligands Lipopolysaccharides Lipopolysaccharides - toxicity Male Medicine Memory Mental disorders Mental health Mitogens Neostriatum Neurology Neurons Neurosurgery Nuclei Nucleus accumbens Nucleus Accumbens - drug effects Nucleus Accumbens - metabolism Nucleus Accumbens - physiopathology Offspring Parvalbumin Prefrontal cortex Prefrontal Cortex - metabolism Prefrontal Cortex - physiopathology Pregnancy Psychiatry Rats Rats, Sprague-Dawley Receptors Receptors, Dopamine D1 - metabolism Receptors, Dopamine D1 - physiology Receptors, Dopamine D2 - metabolism Receptors, Dopamine D2 - physiology Regional development Risk analysis Risk factors Rodents Schizophrenia Studies Synaptic Transmission - drug effects |
title | Effect of maternal lipopolysaccharide administration on the development of dopaminergic receptors and transporter in the rat offspring |
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