Estrogen synthesis in fetal sheep brain: Effect of maternal treatment with an aromatase inhibitor
The aim of the present study was to determine whether the fetal lamb brain has the capacity to aromatize androgens to estrogens during the critical period for sexual differentiation. We also determined whether administration of the aromatase-inhibitor 1,4,6-androstatriene-3,17-dione (ATD) could cros...
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Veröffentlicht in: | Biology of reproduction 2003-02, Vol.68 (2), p.370-374 |
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creator | Roselli, C.E Resko, J.A Stormshak, F |
description | The aim of the present study was to determine whether the fetal lamb brain has the capacity to aromatize androgens to estrogens
during the critical period for sexual differentiation. We also determined whether administration of the aromatase-inhibitor
1,4,6-androstatriene-3,17-dione (ATD) could cross the placenta and inhibit aromatase activity (AA) in fetal brain. Eight pregnant
ewes were utilized. On Day 50 of pregnancy, four ewes were given ATD-filled Silastic implants, and the other four ewes received
sham surgeries. The fetuses were surgically delivered 2 wk later (Day 64 of gestation). High levels of AA (0.8â1.4 pmol/h/mg
protein) were present in the hypothalamus and amygdala. Lower levels (0.02â0.1 pmol/h/mg protein) were measured in brain stem
regions, cortex, and olfactory bulbs. The Michaelis-Menten dissociation constant ( K m ) for aromatase in the fetal sheep brain was 3â4 nM. No significant sex differences in AA were observed in brain. Treatment
with ATD produced significant inhibition of AA in most brain areas but did not significantly alter serum profiles of the major
sex steroids in maternal and fetal serum. Concentrations of testosterone in serum from the umbilical artery and vein were
significantly greater in male than in female fetuses. No other sex differences in serum steroids were observed. These data
demonstrate that high levels of AA are found in the fetal sheep hypothalamus and amygdala during the critical period for sexual
differentiation. They also demonstrate that AA can be inhibited in the fetal lamb brain by treating the mother with ATD, without
harming fetal development. |
doi_str_mv | 10.1095/biolreprod.102.007633 |
format | Article |
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during the critical period for sexual differentiation. We also determined whether administration of the aromatase-inhibitor
1,4,6-androstatriene-3,17-dione (ATD) could cross the placenta and inhibit aromatase activity (AA) in fetal brain. Eight pregnant
ewes were utilized. On Day 50 of pregnancy, four ewes were given ATD-filled Silastic implants, and the other four ewes received
sham surgeries. The fetuses were surgically delivered 2 wk later (Day 64 of gestation). High levels of AA (0.8â1.4 pmol/h/mg
protein) were present in the hypothalamus and amygdala. Lower levels (0.02â0.1 pmol/h/mg protein) were measured in brain stem
regions, cortex, and olfactory bulbs. The Michaelis-Menten dissociation constant ( K m ) for aromatase in the fetal sheep brain was 3â4 nM. No significant sex differences in AA were observed in brain. Treatment
with ATD produced significant inhibition of AA in most brain areas but did not significantly alter serum profiles of the major
sex steroids in maternal and fetal serum. Concentrations of testosterone in serum from the umbilical artery and vein were
significantly greater in male than in female fetuses. No other sex differences in serum steroids were observed. These data
demonstrate that high levels of AA are found in the fetal sheep hypothalamus and amygdala during the critical period for sexual
differentiation. They also demonstrate that AA can be inhibited in the fetal lamb brain by treating the mother with ATD, without
harming fetal development.</description><identifier>ISSN: 0006-3363</identifier><identifier>EISSN: 1529-7268</identifier><identifier>DOI: 10.1095/biolreprod.102.007633</identifier><identifier>PMID: 12533398</identifier><identifier>CODEN: BIREBV</identifier><language>eng</language><publisher>Madison, WI: Society for the Study of Reproduction</publisher><subject>1,4,6-androstatriene-3, 17-dione ; androgen aromatization ; Androgens - blood ; Androstatrienes - pharmacology ; Androstenedione - blood ; Animals ; Aromatase Inhibitors ; Biological and medical sciences ; biosynthesis ; brain ; Brain - embryology ; dams (mothers) ; Dihydrotestosterone - blood ; Embryology: invertebrates and vertebrates. Teratology ; enzyme activity ; enzyme inhibitors ; Enzyme Inhibitors - pharmacology ; estrogens ; Estrogens - biosynthesis ; Estrogens - blood ; ewes ; Female ; Fetal Blood ; fetus ; Fetus - metabolism ; Fundamental and applied biological sciences. Psychology ; gender differences ; hormone secretion ; Male ; Organogenesis. Physiological fonctions ; Physiological fonctions ; pregnancy ; Pregnancy - blood ; Pregnancy - drug effects ; sexual development ; Sexual differentiation and maturation. Puberty. Climacterium ; Sheep ; steroid hormones ; testosterone ; Testosterone - blood ; Vertebrates: reproduction</subject><ispartof>Biology of reproduction, 2003-02, Vol.68 (2), p.370-374</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27907,27908</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14491639$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12533398$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roselli, C.E</creatorcontrib><creatorcontrib>Resko, J.A</creatorcontrib><creatorcontrib>Stormshak, F</creatorcontrib><title>Estrogen synthesis in fetal sheep brain: Effect of maternal treatment with an aromatase inhibitor</title><title>Biology of reproduction</title><addtitle>Biol Reprod</addtitle><description>The aim of the present study was to determine whether the fetal lamb brain has the capacity to aromatize androgens to estrogens
during the critical period for sexual differentiation. We also determined whether administration of the aromatase-inhibitor
1,4,6-androstatriene-3,17-dione (ATD) could cross the placenta and inhibit aromatase activity (AA) in fetal brain. Eight pregnant
ewes were utilized. On Day 50 of pregnancy, four ewes were given ATD-filled Silastic implants, and the other four ewes received
sham surgeries. The fetuses were surgically delivered 2 wk later (Day 64 of gestation). High levels of AA (0.8â1.4 pmol/h/mg
protein) were present in the hypothalamus and amygdala. Lower levels (0.02â0.1 pmol/h/mg protein) were measured in brain stem
regions, cortex, and olfactory bulbs. The Michaelis-Menten dissociation constant ( K m ) for aromatase in the fetal sheep brain was 3â4 nM. No significant sex differences in AA were observed in brain. Treatment
with ATD produced significant inhibition of AA in most brain areas but did not significantly alter serum profiles of the major
sex steroids in maternal and fetal serum. Concentrations of testosterone in serum from the umbilical artery and vein were
significantly greater in male than in female fetuses. No other sex differences in serum steroids were observed. These data
demonstrate that high levels of AA are found in the fetal sheep hypothalamus and amygdala during the critical period for sexual
differentiation. They also demonstrate that AA can be inhibited in the fetal lamb brain by treating the mother with ATD, without
harming fetal development.</description><subject>1,4,6-androstatriene-3, 17-dione</subject><subject>androgen aromatization</subject><subject>Androgens - blood</subject><subject>Androstatrienes - pharmacology</subject><subject>Androstenedione - blood</subject><subject>Animals</subject><subject>Aromatase Inhibitors</subject><subject>Biological and medical sciences</subject><subject>biosynthesis</subject><subject>brain</subject><subject>Brain - embryology</subject><subject>dams (mothers)</subject><subject>Dihydrotestosterone - blood</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>enzyme activity</subject><subject>enzyme inhibitors</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>estrogens</subject><subject>Estrogens - biosynthesis</subject><subject>Estrogens - blood</subject><subject>ewes</subject><subject>Female</subject><subject>Fetal Blood</subject><subject>fetus</subject><subject>Fetus - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gender differences</subject><subject>hormone secretion</subject><subject>Male</subject><subject>Organogenesis. Physiological fonctions</subject><subject>Physiological fonctions</subject><subject>pregnancy</subject><subject>Pregnancy - blood</subject><subject>Pregnancy - drug effects</subject><subject>sexual development</subject><subject>Sexual differentiation and maturation. Puberty. Climacterium</subject><subject>Sheep</subject><subject>steroid hormones</subject><subject>testosterone</subject><subject>Testosterone - blood</subject><subject>Vertebrates: reproduction</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0U1v1DAQBmALgehS-AmAL3BLsT1OYnND1fIhVeIAPVuT7HhjlDiL7VXUf4-lLuppNHofvYcZxt5KcSOFbT8NYZ0TndJ6qLu6EaLvAJ6xnWyVbXrVmedsJ4ToGoAOrtirnP8IITUoeMmupGoBwJodw30uaT1S5PkhlolyyDxE7qngzPNEdOJDwhA_8733NBa-er5goRRrXhJhWSgWvoUycYwc01pTzFRLpjCEsqbX7IXHOdOby7xm91_3v2-_N3c_v_24_XLXeGVlaaQ-GI1orZFGd8J6I8AK1fatBrTGjKRxRKEGrUdtrPQKASR00lftvYdr9vGxt97k75lycUvII80zRlrP2fXKttYIVeG7CzwPCx3cKYUF04P7f5QKPlwA5hFnnzCOIT85ra3swD65KRynLSRyecF5rrXgtm3rjFMOelHd-0fncXV4TLXr_pcSEkR9pO1Awz9CsYmE</recordid><startdate>20030201</startdate><enddate>20030201</enddate><creator>Roselli, C.E</creator><creator>Resko, J.A</creator><creator>Stormshak, F</creator><general>Society for the Study of Reproduction</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20030201</creationdate><title>Estrogen synthesis in fetal sheep brain: Effect of maternal treatment with an aromatase inhibitor</title><author>Roselli, C.E ; Resko, J.A ; Stormshak, F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f291t-14d84aa998184609f80390257543a988ce4aca02b44c4891f2a331361f460fff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>1,4,6-androstatriene-3, 17-dione</topic><topic>androgen aromatization</topic><topic>Androgens - blood</topic><topic>Androstatrienes - pharmacology</topic><topic>Androstenedione - blood</topic><topic>Animals</topic><topic>Aromatase Inhibitors</topic><topic>Biological and medical sciences</topic><topic>biosynthesis</topic><topic>brain</topic><topic>Brain - embryology</topic><topic>dams (mothers)</topic><topic>Dihydrotestosterone - blood</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>enzyme activity</topic><topic>enzyme inhibitors</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>estrogens</topic><topic>Estrogens - biosynthesis</topic><topic>Estrogens - blood</topic><topic>ewes</topic><topic>Female</topic><topic>Fetal Blood</topic><topic>fetus</topic><topic>Fetus - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gender differences</topic><topic>hormone secretion</topic><topic>Male</topic><topic>Organogenesis. Physiological fonctions</topic><topic>Physiological fonctions</topic><topic>pregnancy</topic><topic>Pregnancy - blood</topic><topic>Pregnancy - drug effects</topic><topic>sexual development</topic><topic>Sexual differentiation and maturation. Puberty. Climacterium</topic><topic>Sheep</topic><topic>steroid hormones</topic><topic>testosterone</topic><topic>Testosterone - blood</topic><topic>Vertebrates: reproduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roselli, C.E</creatorcontrib><creatorcontrib>Resko, J.A</creatorcontrib><creatorcontrib>Stormshak, F</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roselli, C.E</au><au>Resko, J.A</au><au>Stormshak, F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Estrogen synthesis in fetal sheep brain: Effect of maternal treatment with an aromatase inhibitor</atitle><jtitle>Biology of reproduction</jtitle><addtitle>Biol Reprod</addtitle><date>2003-02-01</date><risdate>2003</risdate><volume>68</volume><issue>2</issue><spage>370</spage><epage>374</epage><pages>370-374</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><coden>BIREBV</coden><abstract>The aim of the present study was to determine whether the fetal lamb brain has the capacity to aromatize androgens to estrogens
during the critical period for sexual differentiation. We also determined whether administration of the aromatase-inhibitor
1,4,6-androstatriene-3,17-dione (ATD) could cross the placenta and inhibit aromatase activity (AA) in fetal brain. Eight pregnant
ewes were utilized. On Day 50 of pregnancy, four ewes were given ATD-filled Silastic implants, and the other four ewes received
sham surgeries. The fetuses were surgically delivered 2 wk later (Day 64 of gestation). High levels of AA (0.8â1.4 pmol/h/mg
protein) were present in the hypothalamus and amygdala. Lower levels (0.02â0.1 pmol/h/mg protein) were measured in brain stem
regions, cortex, and olfactory bulbs. The Michaelis-Menten dissociation constant ( K m ) for aromatase in the fetal sheep brain was 3â4 nM. No significant sex differences in AA were observed in brain. Treatment
with ATD produced significant inhibition of AA in most brain areas but did not significantly alter serum profiles of the major
sex steroids in maternal and fetal serum. Concentrations of testosterone in serum from the umbilical artery and vein were
significantly greater in male than in female fetuses. No other sex differences in serum steroids were observed. These data
demonstrate that high levels of AA are found in the fetal sheep hypothalamus and amygdala during the critical period for sexual
differentiation. They also demonstrate that AA can be inhibited in the fetal lamb brain by treating the mother with ATD, without
harming fetal development.</abstract><cop>Madison, WI</cop><pub>Society for the Study of Reproduction</pub><pmid>12533398</pmid><doi>10.1095/biolreprod.102.007633</doi><tpages>5</tpages></addata></record> |
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source | MEDLINE; BioOne Complete; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals |
subjects | 1,4,6-androstatriene-3, 17-dione androgen aromatization Androgens - blood Androstatrienes - pharmacology Androstenedione - blood Animals Aromatase Inhibitors Biological and medical sciences biosynthesis brain Brain - embryology dams (mothers) Dihydrotestosterone - blood Embryology: invertebrates and vertebrates. Teratology enzyme activity enzyme inhibitors Enzyme Inhibitors - pharmacology estrogens Estrogens - biosynthesis Estrogens - blood ewes Female Fetal Blood fetus Fetus - metabolism Fundamental and applied biological sciences. Psychology gender differences hormone secretion Male Organogenesis. Physiological fonctions Physiological fonctions pregnancy Pregnancy - blood Pregnancy - drug effects sexual development Sexual differentiation and maturation. Puberty. Climacterium Sheep steroid hormones testosterone Testosterone - blood Vertebrates: reproduction |
title | Estrogen synthesis in fetal sheep brain: Effect of maternal treatment with an aromatase inhibitor |
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