Sex specific changes in placental growth and MAPK following short term maternal dexamethasone exposure in the mouse
Abstract Objectives Maternal glucocorticoid (GC) exposure during pregnancy can alter fetal development and program the onset of disease in adult offspring. The placenta helps protect the fetus from excess GC exposure but is itself susceptible to maternal insults and may be involved in sex dependant...
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Veröffentlicht in: | Placenta (Eastbourne) 2011-12, Vol.32 (12), p.981-989 |
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description | Abstract Objectives Maternal glucocorticoid (GC) exposure during pregnancy can alter fetal development and program the onset of disease in adult offspring. The placenta helps protect the fetus from excess GC exposure but is itself susceptible to maternal insults and may be involved in sex dependant regulation of fetal programming. This study aimed to investigate the effects of maternal GC exposure on the developing placenta. Study design and main outcome measures Pregnant mice were treated with dexamethasone (DEX-1 μg/kg/h) or saline (SAL) for 60 h via minipump beginning at E12.5. Placentas were collected at E14.5 and E17.5 and the expression of growth factors and placental transporters examined by real-time PCR and/or Western blot. Histological analysis was performed to assess for morphological changes. Results At E14.5, DEX exposed male and female fetuses had a lower weight compared to SAL animals but placental weight was lower in females only. Hsd11b2 and Vegfa gene expression was increased and MAPK1 protein expression decreased in the placentas of females only. At E17.5 placental and fetal body weights were similar and differences in MAPK were no longer present although HSD11B2 protein was elevated in placentas of DEX females. Levels of glucose or amino acid transporters were unaffected. Conclusions Results suggest sex specific responses to maternal GCs within the placenta. Decreased levels of MAPK protein in placentas of female fetuses suggest alterations in the MAPK pathway may contribute to the lower placental weights in this sex. This may contribute towards sex specific fetal programming of adult disease. |
doi_str_mv | 10.1016/j.placenta.2011.09.009 |
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The placenta helps protect the fetus from excess GC exposure but is itself susceptible to maternal insults and may be involved in sex dependant regulation of fetal programming. This study aimed to investigate the effects of maternal GC exposure on the developing placenta. Study design and main outcome measures Pregnant mice were treated with dexamethasone (DEX-1 μg/kg/h) or saline (SAL) for 60 h via minipump beginning at E12.5. Placentas were collected at E14.5 and E17.5 and the expression of growth factors and placental transporters examined by real-time PCR and/or Western blot. Histological analysis was performed to assess for morphological changes. Results At E14.5, DEX exposed male and female fetuses had a lower weight compared to SAL animals but placental weight was lower in females only. Hsd11b2 and Vegfa gene expression was increased and MAPK1 protein expression decreased in the placentas of females only. At E17.5 placental and fetal body weights were similar and differences in MAPK were no longer present although HSD11B2 protein was elevated in placentas of DEX females. Levels of glucose or amino acid transporters were unaffected. Conclusions Results suggest sex specific responses to maternal GCs within the placenta. Decreased levels of MAPK protein in placentas of female fetuses suggest alterations in the MAPK pathway may contribute to the lower placental weights in this sex. This may contribute towards sex specific fetal programming of adult disease.</description><identifier>ISSN: 0143-4004</identifier><identifier>EISSN: 1532-3102</identifier><identifier>DOI: 10.1016/j.placenta.2011.09.009</identifier><identifier>PMID: 21974799</identifier><identifier>CODEN: PLACDF</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>11-beta-Hydroxysteroid Dehydrogenase Type 2 - biosynthesis ; Animals ; Biological and medical sciences ; Dexamethasone - pharmacology ; Embryology: invertebrates and vertebrates. Teratology ; Female ; Fetal programming ; Fetus - drug effects ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation, Developmental - drug effects ; Glucocorticoids ; Hsd11b2 ; Internal Medicine ; Male ; Mice ; Mice, Inbred C57BL ; Mitogen-Activated Protein Kinase 1 - biosynthesis ; Obstetrics and Gynecology ; Organ Size - drug effects ; Placenta - drug effects ; Placenta - pathology ; Placentation ; Pregnancy ; Receptors, Glucocorticoid - biosynthesis ; Sex Factors ; Vascular Endothelial Growth Factor A - biosynthesis ; Vegf</subject><ispartof>Placenta (Eastbourne), 2011-12, Vol.32 (12), p.981-989</ispartof><rights>Elsevier Ltd</rights><rights>2011 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c452t-aaa1295257e54abe614407665e1f47209181c3e79f4a0a01c7999a2a4acf69e93</citedby><cites>FETCH-LOGICAL-c452t-aaa1295257e54abe614407665e1f47209181c3e79f4a0a01c7999a2a4acf69e93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0143400411004541$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25281726$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21974799$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cuffe, J.S.M</creatorcontrib><creatorcontrib>Dickinson, H</creatorcontrib><creatorcontrib>Simmons, D.G</creatorcontrib><creatorcontrib>Moritz, K.M</creatorcontrib><title>Sex specific changes in placental growth and MAPK following short term maternal dexamethasone exposure in the mouse</title><title>Placenta (Eastbourne)</title><addtitle>Placenta</addtitle><description>Abstract Objectives Maternal glucocorticoid (GC) exposure during pregnancy can alter fetal development and program the onset of disease in adult offspring. The placenta helps protect the fetus from excess GC exposure but is itself susceptible to maternal insults and may be involved in sex dependant regulation of fetal programming. This study aimed to investigate the effects of maternal GC exposure on the developing placenta. Study design and main outcome measures Pregnant mice were treated with dexamethasone (DEX-1 μg/kg/h) or saline (SAL) for 60 h via minipump beginning at E12.5. Placentas were collected at E14.5 and E17.5 and the expression of growth factors and placental transporters examined by real-time PCR and/or Western blot. Histological analysis was performed to assess for morphological changes. Results At E14.5, DEX exposed male and female fetuses had a lower weight compared to SAL animals but placental weight was lower in females only. Hsd11b2 and Vegfa gene expression was increased and MAPK1 protein expression decreased in the placentas of females only. At E17.5 placental and fetal body weights were similar and differences in MAPK were no longer present although HSD11B2 protein was elevated in placentas of DEX females. Levels of glucose or amino acid transporters were unaffected. Conclusions Results suggest sex specific responses to maternal GCs within the placenta. Decreased levels of MAPK protein in placentas of female fetuses suggest alterations in the MAPK pathway may contribute to the lower placental weights in this sex. This may contribute towards sex specific fetal programming of adult disease.</description><subject>11-beta-Hydroxysteroid Dehydrogenase Type 2 - biosynthesis</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Dexamethasone - pharmacology</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Female</subject><subject>Fetal programming</subject><subject>Fetus - drug effects</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation, Developmental - drug effects</subject><subject>Glucocorticoids</subject><subject>Hsd11b2</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mitogen-Activated Protein Kinase 1 - biosynthesis</subject><subject>Obstetrics and Gynecology</subject><subject>Organ Size - drug effects</subject><subject>Placenta - drug effects</subject><subject>Placenta - pathology</subject><subject>Placentation</subject><subject>Pregnancy</subject><subject>Receptors, Glucocorticoid - biosynthesis</subject><subject>Sex Factors</subject><subject>Vascular Endothelial Growth Factor A - biosynthesis</subject><subject>Vegf</subject><issn>0143-4004</issn><issn>1532-3102</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk1v1DAQhiMEokvhL1S-IE5JPY6T1BdEVZUPtQikwtmaOpONl8Re7IRu_z2OdhckLlw8l2fesR9Plp0BL4BDfb4ptgMachMWggMUXBWcqyfZCqpS5CVw8TRbcZBlLjmXJ9mLGDc8ERLE8-xEgGpko9Qqi3e0Y3FLxnbWMNOjW1Nk1rFj_MDWwT9MPUPXss-XX29Y54fBP1i3ZrH3YWIThZGNmIpLdEs7HGnqMXpHjHZbH-dAS-LUExv9HOll9qzDIdKrQz3Nvr-__nb1Mb_98uHT1eVtbmQlphwRQahKVA1VEu-pBil5U9cVQScbwRVcgCmpUZ1EjhxMepBCgRJNVytS5Wn2Zp-7Df7nTHHSo42GhgEdpXtoxRteCpALWe9JE3yMgTq9DXbE8KiB68W33uijEL341lzpZDM1nh1GzPcjtX_ajoIT8PoAYDQ4dAGdsfEvV4kLaESduHd7jpKQX5aCjsaSM9TaQGbSrbf_v8vbfyLMYJ1NU3_QI8WNn5cPihp0FJrru2U7luUASEclofwNAfe3Qw</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Cuffe, J.S.M</creator><creator>Dickinson, H</creator><creator>Simmons, D.G</creator><creator>Moritz, K.M</creator><general>Elsevier Ltd</general><general>Elsevier</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>7X8</scope></search><sort><creationdate>20111201</creationdate><title>Sex specific changes in placental growth and MAPK following short term maternal dexamethasone exposure in the mouse</title><author>Cuffe, J.S.M ; Dickinson, H ; Simmons, D.G ; Moritz, K.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-aaa1295257e54abe614407665e1f47209181c3e79f4a0a01c7999a2a4acf69e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>11-beta-Hydroxysteroid Dehydrogenase Type 2 - biosynthesis</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Dexamethasone - pharmacology</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Female</topic><topic>Fetal programming</topic><topic>Fetus - drug effects</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation, Developmental - drug effects</topic><topic>Glucocorticoids</topic><topic>Hsd11b2</topic><topic>Internal Medicine</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mitogen-Activated Protein Kinase 1 - biosynthesis</topic><topic>Obstetrics and Gynecology</topic><topic>Organ Size - drug effects</topic><topic>Placenta - drug effects</topic><topic>Placenta - pathology</topic><topic>Placentation</topic><topic>Pregnancy</topic><topic>Receptors, Glucocorticoid - biosynthesis</topic><topic>Sex Factors</topic><topic>Vascular Endothelial Growth Factor A - biosynthesis</topic><topic>Vegf</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cuffe, J.S.M</creatorcontrib><creatorcontrib>Dickinson, H</creatorcontrib><creatorcontrib>Simmons, D.G</creatorcontrib><creatorcontrib>Moritz, K.M</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>MEDLINE - Academic</collection><jtitle>Placenta (Eastbourne)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cuffe, J.S.M</au><au>Dickinson, H</au><au>Simmons, D.G</au><au>Moritz, K.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sex specific changes in placental growth and MAPK following short term maternal dexamethasone exposure in the mouse</atitle><jtitle>Placenta (Eastbourne)</jtitle><addtitle>Placenta</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>32</volume><issue>12</issue><spage>981</spage><epage>989</epage><pages>981-989</pages><issn>0143-4004</issn><eissn>1532-3102</eissn><coden>PLACDF</coden><abstract>Abstract Objectives Maternal glucocorticoid (GC) exposure during pregnancy can alter fetal development and program the onset of disease in adult offspring. The placenta helps protect the fetus from excess GC exposure but is itself susceptible to maternal insults and may be involved in sex dependant regulation of fetal programming. This study aimed to investigate the effects of maternal GC exposure on the developing placenta. Study design and main outcome measures Pregnant mice were treated with dexamethasone (DEX-1 μg/kg/h) or saline (SAL) for 60 h via minipump beginning at E12.5. Placentas were collected at E14.5 and E17.5 and the expression of growth factors and placental transporters examined by real-time PCR and/or Western blot. Histological analysis was performed to assess for morphological changes. Results At E14.5, DEX exposed male and female fetuses had a lower weight compared to SAL animals but placental weight was lower in females only. Hsd11b2 and Vegfa gene expression was increased and MAPK1 protein expression decreased in the placentas of females only. At E17.5 placental and fetal body weights were similar and differences in MAPK were no longer present although HSD11B2 protein was elevated in placentas of DEX females. Levels of glucose or amino acid transporters were unaffected. Conclusions Results suggest sex specific responses to maternal GCs within the placenta. Decreased levels of MAPK protein in placentas of female fetuses suggest alterations in the MAPK pathway may contribute to the lower placental weights in this sex. This may contribute towards sex specific fetal programming of adult disease.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>21974799</pmid><doi>10.1016/j.placenta.2011.09.009</doi><tpages>9</tpages></addata></record> |
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subjects | 11-beta-Hydroxysteroid Dehydrogenase Type 2 - biosynthesis Animals Biological and medical sciences Dexamethasone - pharmacology Embryology: invertebrates and vertebrates. Teratology Female Fetal programming Fetus - drug effects Fundamental and applied biological sciences. Psychology Gene Expression Regulation, Developmental - drug effects Glucocorticoids Hsd11b2 Internal Medicine Male Mice Mice, Inbred C57BL Mitogen-Activated Protein Kinase 1 - biosynthesis Obstetrics and Gynecology Organ Size - drug effects Placenta - drug effects Placenta - pathology Placentation Pregnancy Receptors, Glucocorticoid - biosynthesis Sex Factors Vascular Endothelial Growth Factor A - biosynthesis Vegf |
title | Sex specific changes in placental growth and MAPK following short term maternal dexamethasone exposure in the mouse |
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