Distribution and sex differences in aromatase-producing neurons in the brain of Japanese quail embryos
The biochemical properties, neuroanatomical location, and function of aromatase (ARO), the enzyme that converts testosterone to 17β-estradiol, have been studied extensively in the adult quail brain. Conversely, very little is known about ARO in quail embryos. This study investigated the distribution...
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description | The biochemical properties, neuroanatomical location, and function of aromatase (ARO), the enzyme that converts testosterone to 17β-estradiol, have been studied extensively in the adult quail brain. Conversely, very little is known about ARO in quail embryos. This study investigated the distribution of ARO in quail prosencephalon at embryonic days (E) 9, 11, and 15 by immunocytochemistry. ARO-immunoreactive cells were observed within the walls of the cerebral ventricles, the ventral striatum, medial preoptic nucleus (POM), medial part of the bed nucleus of the stria terminalis (BSTM), lateral part of the BST, and in the tuberal region. The BSTM and to a lesser extent the POM showed transient, female-biased sex-differences. In the BSTM, the number of the ARO-immunoreactive cells, the fractional area covered by ARO-immunoreactive structures, and the overall extension of ARO-immunoreactivity were greater in females at E9 and E11, but these differences largely disappeared at E15 and post-hatch day 1. The sex differences were confirmed at the transcriptional level by
in situ hybridization. In the lateral part of the POM, females showed slightly more ARO-immunoreactivity than males at E11. Treatment of E9 male embryos with estradiol completely feminized ARO-immunoreactivity at E11. The origins and the functional significance of these sex differences remain unknown. |
doi_str_mv | 10.1016/j.jchemneu.2010.02.003 |
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in situ hybridization. In the lateral part of the POM, females showed slightly more ARO-immunoreactivity than males at E11. Treatment of E9 male embryos with estradiol completely feminized ARO-immunoreactivity at E11. The origins and the functional significance of these sex differences remain unknown.</description><identifier>ISSN: 0891-0618</identifier><identifier>EISSN: 1873-6300</identifier><identifier>DOI: 10.1016/j.jchemneu.2010.02.003</identifier><identifier>PMID: 20188162</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Aromatase - genetics ; Aromatase - metabolism ; Bed nucleus of the stria terminalis ; Bird ; Brain Mapping ; Coturnix - embryology ; Coturnix japonica ; Development ; Estradiol ; Estradiol - biosynthesis ; Estradiol - pharmacology ; Female ; Immunohistochemistry ; Male ; Nerve Net - cytology ; Nerve Net - embryology ; Nerve Net - enzymology ; Neurons - cytology ; Neurons - enzymology ; Preoptic area ; Preoptic Area - cytology ; Preoptic Area - enzymology ; Prosencephalon - cytology ; Prosencephalon - embryology ; Prosencephalon - enzymology ; RNA, Messenger - metabolism ; Septal Nuclei - cytology ; Septal Nuclei - enzymology ; Sex Characteristics ; Sex Differentiation - physiology ; Steroids</subject><ispartof>Journal of chemical neuroanatomy, 2010-07, Vol.39 (4), p.272-288</ispartof><rights>2010 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-7fa1cd895e8d1b5831a0ba193f6bcfc4b68c3a1fdc5a004b74e8c48e5620b71d3</citedby><cites>FETCH-LOGICAL-c465t-7fa1cd895e8d1b5831a0ba193f6bcfc4b68c3a1fdc5a004b74e8c48e5620b71d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jchemneu.2010.02.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20188162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aste, Nicoletta</creatorcontrib><creatorcontrib>Watanabe, Yumi</creatorcontrib><creatorcontrib>Harada, Nobuhiro</creatorcontrib><creatorcontrib>Saito, Noboru</creatorcontrib><title>Distribution and sex differences in aromatase-producing neurons in the brain of Japanese quail embryos</title><title>Journal of chemical neuroanatomy</title><addtitle>J Chem Neuroanat</addtitle><description>The biochemical properties, neuroanatomical location, and function of aromatase (ARO), the enzyme that converts testosterone to 17β-estradiol, have been studied extensively in the adult quail brain. Conversely, very little is known about ARO in quail embryos. This study investigated the distribution of ARO in quail prosencephalon at embryonic days (E) 9, 11, and 15 by immunocytochemistry. ARO-immunoreactive cells were observed within the walls of the cerebral ventricles, the ventral striatum, medial preoptic nucleus (POM), medial part of the bed nucleus of the stria terminalis (BSTM), lateral part of the BST, and in the tuberal region. The BSTM and to a lesser extent the POM showed transient, female-biased sex-differences. In the BSTM, the number of the ARO-immunoreactive cells, the fractional area covered by ARO-immunoreactive structures, and the overall extension of ARO-immunoreactivity were greater in females at E9 and E11, but these differences largely disappeared at E15 and post-hatch day 1. The sex differences were confirmed at the transcriptional level by
in situ hybridization. In the lateral part of the POM, females showed slightly more ARO-immunoreactivity than males at E11. Treatment of E9 male embryos with estradiol completely feminized ARO-immunoreactivity at E11. The origins and the functional significance of these sex differences remain unknown.</description><subject>Animals</subject><subject>Aromatase - genetics</subject><subject>Aromatase - metabolism</subject><subject>Bed nucleus of the stria terminalis</subject><subject>Bird</subject><subject>Brain Mapping</subject><subject>Coturnix - embryology</subject><subject>Coturnix japonica</subject><subject>Development</subject><subject>Estradiol</subject><subject>Estradiol - biosynthesis</subject><subject>Estradiol - pharmacology</subject><subject>Female</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Nerve Net - cytology</subject><subject>Nerve Net - embryology</subject><subject>Nerve Net - enzymology</subject><subject>Neurons - cytology</subject><subject>Neurons - enzymology</subject><subject>Preoptic area</subject><subject>Preoptic Area - cytology</subject><subject>Preoptic Area - enzymology</subject><subject>Prosencephalon - cytology</subject><subject>Prosencephalon - embryology</subject><subject>Prosencephalon - enzymology</subject><subject>RNA, Messenger - metabolism</subject><subject>Septal Nuclei - cytology</subject><subject>Septal Nuclei - enzymology</subject><subject>Sex Characteristics</subject><subject>Sex Differentiation - physiology</subject><subject>Steroids</subject><issn>0891-0618</issn><issn>1873-6300</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv2zAQhImiQe0m_QsBbz3JWYoSRd1auHm0CNBLcib4WDY0LNEmpSL596HruNecSCy_4SxmCLlksGLAxNVmtbFPOIw4r2ooQ6hXAPwDWTLZ8UpwgI9kCbJnFQgmF-RzzhsA1vJGfCKLIpGSiXpJ_I-QpxTMPIU4Uj06mvGZuuA9JhwtZhrKOMVBTzpjtUvRzTaMf2hxTnH89zw9ITVJl1v09Jfe6REz0v2sw5biYNJLzBfkzOttxi9v5zl5vLl-WN9V979vf66_31e2Ee1UdV4z62TfonTMtJIzDUaznnthrLeNEdJyzbyzrQZoTNegtI3EVtRgOub4Ofl6_Lcsup8xT2oI2eJ2W3aKc1ZdI-q674V4n-ScgyxgIcWRtCnmnNCrXQqDTi-KgTqUoTbqVIY6lKGgVqWMIrx8s5jNgO6_7JR-Ab4dASyR_A2YVLbhkLoLCe2kXAzvebwC9kSgHg</recordid><startdate>20100701</startdate><enddate>20100701</enddate><creator>Aste, Nicoletta</creator><creator>Watanabe, Yumi</creator><creator>Harada, Nobuhiro</creator><creator>Saito, Noboru</creator><general>Elsevier B.V</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>7X8</scope><scope>7TK</scope></search><sort><creationdate>20100701</creationdate><title>Distribution and sex differences in aromatase-producing neurons in the brain of Japanese quail embryos</title><author>Aste, Nicoletta ; Watanabe, Yumi ; Harada, Nobuhiro ; Saito, Noboru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-7fa1cd895e8d1b5831a0ba193f6bcfc4b68c3a1fdc5a004b74e8c48e5620b71d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Aromatase - genetics</topic><topic>Aromatase - metabolism</topic><topic>Bed nucleus of the stria terminalis</topic><topic>Bird</topic><topic>Brain Mapping</topic><topic>Coturnix - embryology</topic><topic>Coturnix japonica</topic><topic>Development</topic><topic>Estradiol</topic><topic>Estradiol - biosynthesis</topic><topic>Estradiol - pharmacology</topic><topic>Female</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Nerve Net - cytology</topic><topic>Nerve Net - embryology</topic><topic>Nerve Net - enzymology</topic><topic>Neurons - cytology</topic><topic>Neurons - enzymology</topic><topic>Preoptic area</topic><topic>Preoptic Area - cytology</topic><topic>Preoptic Area - enzymology</topic><topic>Prosencephalon - cytology</topic><topic>Prosencephalon - embryology</topic><topic>Prosencephalon - enzymology</topic><topic>RNA, Messenger - metabolism</topic><topic>Septal Nuclei - cytology</topic><topic>Septal Nuclei - enzymology</topic><topic>Sex Characteristics</topic><topic>Sex Differentiation - physiology</topic><topic>Steroids</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aste, Nicoletta</creatorcontrib><creatorcontrib>Watanabe, Yumi</creatorcontrib><creatorcontrib>Harada, Nobuhiro</creatorcontrib><creatorcontrib>Saito, Noboru</creatorcontrib><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><collection>Neurosciences Abstracts</collection><jtitle>Journal of chemical neuroanatomy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aste, Nicoletta</au><au>Watanabe, Yumi</au><au>Harada, Nobuhiro</au><au>Saito, Noboru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distribution and sex differences in aromatase-producing neurons in the brain of Japanese quail embryos</atitle><jtitle>Journal of chemical neuroanatomy</jtitle><addtitle>J Chem Neuroanat</addtitle><date>2010-07-01</date><risdate>2010</risdate><volume>39</volume><issue>4</issue><spage>272</spage><epage>288</epage><pages>272-288</pages><issn>0891-0618</issn><eissn>1873-6300</eissn><abstract>The biochemical properties, neuroanatomical location, and function of aromatase (ARO), the enzyme that converts testosterone to 17β-estradiol, have been studied extensively in the adult quail brain. Conversely, very little is known about ARO in quail embryos. This study investigated the distribution of ARO in quail prosencephalon at embryonic days (E) 9, 11, and 15 by immunocytochemistry. ARO-immunoreactive cells were observed within the walls of the cerebral ventricles, the ventral striatum, medial preoptic nucleus (POM), medial part of the bed nucleus of the stria terminalis (BSTM), lateral part of the BST, and in the tuberal region. The BSTM and to a lesser extent the POM showed transient, female-biased sex-differences. In the BSTM, the number of the ARO-immunoreactive cells, the fractional area covered by ARO-immunoreactive structures, and the overall extension of ARO-immunoreactivity were greater in females at E9 and E11, but these differences largely disappeared at E15 and post-hatch day 1. The sex differences were confirmed at the transcriptional level by
in situ hybridization. In the lateral part of the POM, females showed slightly more ARO-immunoreactivity than males at E11. Treatment of E9 male embryos with estradiol completely feminized ARO-immunoreactivity at E11. The origins and the functional significance of these sex differences remain unknown.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>20188162</pmid><doi>10.1016/j.jchemneu.2010.02.003</doi><tpages>17</tpages></addata></record> |
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subjects | Animals Aromatase - genetics Aromatase - metabolism Bed nucleus of the stria terminalis Bird Brain Mapping Coturnix - embryology Coturnix japonica Development Estradiol Estradiol - biosynthesis Estradiol - pharmacology Female Immunohistochemistry Male Nerve Net - cytology Nerve Net - embryology Nerve Net - enzymology Neurons - cytology Neurons - enzymology Preoptic area Preoptic Area - cytology Preoptic Area - enzymology Prosencephalon - cytology Prosencephalon - embryology Prosencephalon - enzymology RNA, Messenger - metabolism Septal Nuclei - cytology Septal Nuclei - enzymology Sex Characteristics Sex Differentiation - physiology Steroids |
title | Distribution and sex differences in aromatase-producing neurons in the brain of Japanese quail embryos |
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