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
Hauptverfasser: Roselli, C.E, Resko, J.A, Stormshak, F
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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 (0.8–1.4 pmol/h/mg protein) were present in the hypothalamus and amygdala. Lower levels (0.02–0.1 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 3–4 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.
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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 (0.8–1.4 pmol/h/mg protein) were present in the hypothalamus and amygdala. Lower levels (0.02–0.1 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 3–4 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. 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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 (0.8–1.4 pmol/h/mg protein) were present in the hypothalamus and amygdala. Lower levels (0.02–0.1 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 3–4 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 (0.8–1.4 pmol/h/mg protein) were present in the hypothalamus and amygdala. Lower levels (0.02–0.1 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 3–4 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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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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