Occurrence and in vitro biosynthesis of 11-ketotestosterone in Siberian sturgeon, Acipenser baeri Brandt maturing females
Identifieur interne : 000D05 ( Istex/Corpus ); précédent : 000D04; suivant : 000D06Occurrence and in vitro biosynthesis of 11-ketotestosterone in Siberian sturgeon, Acipenser baeri Brandt maturing females
Auteurs : B. Cuisset ; A. Fostier ; P. Williot ; C. Bennetau-Pelissero ; F. Le MennSource :
- Fish Physiology and Biochemistry [ 0920-1742 ] ; 1995-08-01.
Abstract
Abstract: High levels of 11-ketotestosterone (11KT) were found (49 to 160 ng ml−1) in plasma of Siberian sturgeon females during the end of their reproductive cycle. These levels were measured either by specific radioimmunoassay, or both by specific radioimmunoassay and by UV absorption after HPLC (isocratic conditions, 33% methanol, 26% acetonitrile, 41% water). In order to find the origin of 11KT synthesis, ovaries were incubated (30 min and 2h at 20°C) with tritiated 17-hydroxyprogesterone (17OHP) or with tritiated androstenedione (A4). Testosterone (conversion rate from tritiated 17OHP: 4%) and 11-ketotestosterone (conversion rate from tritiated A4: 1.6%) were identified as metabolites of respectively 17OHP and A4 (TLC, HPLC and crystallization). 11β-hydroxyandrostenedione (11βOHA4) and 11β-hydroxytestosterone (11βOHT) were suggested to be intermediate metabolites. Besides interrenal and blood cells were incubated respectively with tritiated cortisol and tritiated A4. 11βOHA4 was identified in interrenal incubation (yield from tritiated cortisol: 1.2%). 11KT in interrenal (yield from tritiated cortisol: 0.14%), and 11βOHA4 and 11KT in blood cells (yield from tritiated A4: 1.6%), were suspected to be synthesized (TLC, HPLC, acetylation). No significant metabolization of tritiated cortisol could be found in liver. The possible contribution of each of these tissues to high 11KT levels found in plasma is discussed.
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DOI: 10.1007/BF00004069
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ISTEX:89AA26D114C8C03C08AFCAFA40A8CB705CBF6094Le document en format XML
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Cuisset</name><affiliation><mods:affiliation>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</mods:affiliation></affiliation></author><author><name sortKey="Fostier, A" sort="Fostier, A" uniqKey="Fostier A" first="A." last="Fostier">A. Fostier</name><affiliation><mods:affiliation>Institut National de la Recherche Agronomique, Laboratoire de Physiologie des Poissons, Campus de Beaulieu, 35042, Rennes Cedex, France</mods:affiliation></affiliation></author><author><name sortKey="Williot, P" sort="Williot, P" uniqKey="Williot P" first="P." last="Williot">P. Williot</name><affiliation><mods:affiliation>Division Aquaculture et Pechê, Centre National du Machinisme Agricole, du Génie Rural, des Eaux des Forêts, 50 Avenue de Verdun, BP 3, 33611, Gazinet Cedex, France</mods:affiliation></affiliation></author><author><name sortKey="Bennetau Pelissero, C" sort="Bennetau Pelissero, C" uniqKey="Bennetau Pelissero C" first="C." last="Bennetau-Pelissero">C. Bennetau-Pelissero</name><affiliation><mods:affiliation>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</mods:affiliation></affiliation><affiliation><mods:affiliation>ENITA Bordeaux, 33170, Gradigham, France</mods:affiliation></affiliation></author><author><name sortKey="Le Menn, F" sort="Le Menn, F" uniqKey="Le Menn F" first="F." last="Le Menn">F. Le Menn</name><affiliation><mods:affiliation>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">Fish Physiology and Biochemistry</title><title level="j" type="abbrev">Fish Physiol Biochem</title><idno type="ISSN">0920-1742</idno><idno type="eISSN">1573-5168</idno><imprint><publisher>Kluwer Academic Publishers</publisher><pubPlace>Dordrecht</pubPlace><date type="published" when="1995-08-01">1995-08-01</date><biblScope unit="volume">14</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="313">313</biblScope><biblScope unit="page" to="322">322</biblScope></imprint><idno type="ISSN">0920-1742</idno></series><idno type="istex">89AA26D114C8C03C08AFCAFA40A8CB705CBF6094</idno><idno type="DOI">10.1007/BF00004069</idno><idno type="ArticleID">BF00004069</idno><idno type="ArticleID">Art6</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0920-1742</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: High levels of 11-ketotestosterone (11KT) were found (49 to 160 ng ml−1) in plasma of Siberian sturgeon females during the end of their reproductive cycle. These levels were measured either by specific radioimmunoassay, or both by specific radioimmunoassay and by UV absorption after HPLC (isocratic conditions, 33% methanol, 26% acetonitrile, 41% water). In order to find the origin of 11KT synthesis, ovaries were incubated (30 min and 2h at 20°C) with tritiated 17-hydroxyprogesterone (17OHP) or with tritiated androstenedione (A4). Testosterone (conversion rate from tritiated 17OHP: 4%) and 11-ketotestosterone (conversion rate from tritiated A4: 1.6%) were identified as metabolites of respectively 17OHP and A4 (TLC, HPLC and crystallization). 11β-hydroxyandrostenedione (11βOHA4) and 11β-hydroxytestosterone (11βOHT) were suggested to be intermediate metabolites. Besides interrenal and blood cells were incubated respectively with tritiated cortisol and tritiated A4. 11βOHA4 was identified in interrenal incubation (yield from tritiated cortisol: 1.2%). 11KT in interrenal (yield from tritiated cortisol: 0.14%), and 11βOHA4 and 11KT in blood cells (yield from tritiated A4: 1.6%), were suspected to be synthesized (TLC, HPLC, acetylation). No significant metabolization of tritiated cortisol could be found in liver. The possible contribution of each of these tissues to high 11KT levels found in plasma is discussed.</div></front></TEI><istex><corpusName>springer</corpusName><author><json:item><name>B. Cuisset</name><affiliations><json:string>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</json:string></affiliations></json:item><json:item><name>A. 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Le Menn</name><affiliations><json:string>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</json:string></affiliations></json:item></author><articleId><json:string>BF00004069</json:string><json:string>Art6</json:string></articleId><language><json:string>eng</json:string></language><originalGenre><json:string>OriginalPaper</json:string></originalGenre><abstract>Abstract: High levels of 11-ketotestosterone (11KT) were found (49 to 160 ng ml−1) in plasma of Siberian sturgeon females during the end of their reproductive cycle. These levels were measured either by specific radioimmunoassay, or both by specific radioimmunoassay and by UV absorption after HPLC (isocratic conditions, 33% methanol, 26% acetonitrile, 41% water). In order to find the origin of 11KT synthesis, ovaries were incubated (30 min and 2h at 20°C) with tritiated 17-hydroxyprogesterone (17OHP) or with tritiated androstenedione (A4). Testosterone (conversion rate from tritiated 17OHP: 4%) and 11-ketotestosterone (conversion rate from tritiated A4: 1.6%) were identified as metabolites of respectively 17OHP and A4 (TLC, HPLC and crystallization). 11β-hydroxyandrostenedione (11βOHA4) and 11β-hydroxytestosterone (11βOHT) were suggested to be intermediate metabolites. Besides interrenal and blood cells were incubated respectively with tritiated cortisol and tritiated A4. 11βOHA4 was identified in interrenal incubation (yield from tritiated cortisol: 1.2%). 11KT in interrenal (yield from tritiated cortisol: 0.14%), and 11βOHA4 and 11KT in blood cells (yield from tritiated A4: 1.6%), were suspected to be synthesized (TLC, HPLC, acetylation). No significant metabolization of tritiated cortisol could be found in liver. 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maturing females</title><respStmt><resp>Références bibliographiques récupérées via GROBID</resp><name resp="ISTEX-API">ISTEX-API (INIST-CNRS)</name></respStmt><respStmt><resp>Références bibliographiques récupérées via GROBID</resp><name resp="ISTEX-API">ISTEX-API (INIST-CNRS)</name></respStmt></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Kluwer Academic Publishers</publisher><pubPlace>Dordrecht</pubPlace><availability><p>Kugler Publications, 1995</p></availability><date>1995</date></publicationStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a" type="main" xml:lang="en">Occurrence and in vitro biosynthesis of 11-ketotestosterone in Siberian sturgeon, Acipenser baeri Brandt maturing females</title><author xml:id="author-1"><persName><forename type="first">B.</forename><surname>Cuisset</surname></persName><affiliation>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</affiliation></author><author xml:id="author-2"><persName><forename type="first">A.</forename><surname>Fostier</surname></persName><affiliation>Institut National de la Recherche Agronomique, Laboratoire de Physiologie des Poissons, Campus de Beaulieu, 35042, Rennes Cedex, France</affiliation></author><author xml:id="author-3"><persName><forename type="first">P.</forename><surname>Williot</surname></persName><affiliation>Division Aquaculture et Pechê, Centre National du Machinisme Agricole, du Génie Rural, des Eaux des Forêts, 50 Avenue de Verdun, BP 3, 33611, Gazinet Cedex, France</affiliation></author><author xml:id="author-4"><persName><forename type="first">C.</forename><surname>Bennetau-Pelissero</surname></persName><affiliation>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</affiliation><affiliation>ENITA Bordeaux, 33170, Gradigham, France</affiliation></author><author xml:id="author-5"><persName><forename type="first">F.</forename><surname>Le Menn</surname></persName><affiliation>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</affiliation></author></analytic><monogr><title level="j">Fish Physiology and Biochemistry</title><title level="j" type="abbrev">Fish Physiol Biochem</title><idno type="journal-ID">10695</idno><idno type="pISSN">0920-1742</idno><idno type="eISSN">1573-5168</idno><idno type="issue-article-count">8</idno><idno type="volume-issue-count">6</idno><imprint><publisher>Kluwer Academic Publishers</publisher><pubPlace>Dordrecht</pubPlace><date type="published" when="1995-08-01"></date><biblScope unit="volume">14</biblScope><biblScope unit="issue">4</biblScope><biblScope unit="page" from="313">313</biblScope><biblScope unit="page" to="322">322</biblScope></imprint></monogr><idno type="istex">89AA26D114C8C03C08AFCAFA40A8CB705CBF6094</idno><idno type="DOI">10.1007/BF00004069</idno><idno type="ArticleID">BF00004069</idno><idno type="ArticleID">Art6</idno></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1995</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Abstract: High levels of 11-ketotestosterone (11KT) were found (49 to 160 ng ml−1) in plasma of Siberian sturgeon females during the end of their reproductive cycle. These levels were measured either by specific radioimmunoassay, or both by specific radioimmunoassay and by UV absorption after HPLC (isocratic conditions, 33% methanol, 26% acetonitrile, 41% water). In order to find the origin of 11KT synthesis, ovaries were incubated (30 min and 2h at 20°C) with tritiated 17-hydroxyprogesterone (17OHP) or with tritiated androstenedione (A4). Testosterone (conversion rate from tritiated 17OHP: 4%) and 11-ketotestosterone (conversion rate from tritiated A4: 1.6%) were identified as metabolites of respectively 17OHP and A4 (TLC, HPLC and crystallization). 11β-hydroxyandrostenedione (11βOHA4) and 11β-hydroxytestosterone (11βOHT) were suggested to be intermediate metabolites. Besides interrenal and blood cells were incubated respectively with tritiated cortisol and tritiated A4. 11βOHA4 was identified in interrenal incubation (yield from tritiated cortisol: 1.2%). 11KT in interrenal (yield from tritiated cortisol: 0.14%), and 11βOHA4 and 11KT in blood cells (yield from tritiated A4: 1.6%), were suspected to be synthesized (TLC, HPLC, acetylation). No significant metabolization of tritiated cortisol could be found in liver. The possible contribution of each of these tissues to high 11KT levels found in plasma is discussed.</p></abstract><textClass><keywords scheme="Journal Subject"><list><head>Life Sciences</head><item><term>Animal Biochemistry</term></item><item><term>Hydrobiology</term></item><item><term>Zoology</term></item><item><term>Animal Anatomy / Morphology / Histology</term></item><item><term>Animal Physiology</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1995-08-01">Published</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2016-11-22">References added</change><change xml:id="refBibs-istex" who="#ISTEX-API" when="2017-01-20">References added</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/89AA26D114C8C03C08AFCAFA40A8CB705CBF6094/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml 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ContainsESM="No"><ArticleID>BF00004069</ArticleID><ArticleDOI>10.1007/BF00004069</ArticleDOI><ArticleSequenceNumber>6</ArticleSequenceNumber><ArticleTitle Language="En">Occurrence and <Emphasis Type="Italic">in vitro</Emphasis> biosynthesis of 11-ketotestosterone in Siberian sturgeon, <Emphasis Type="Italic">Acipenser baeri</Emphasis> Brandt maturing females</ArticleTitle><ArticleFirstPage>313</ArticleFirstPage><ArticleLastPage>322</ArticleLastPage><ArticleHistory><RegistrationDate><Year>2004</Year><Month>3</Month><Day>23</Day></RegistrationDate><Accepted><Year>1995</Year><Month>1</Month><Day>12</Day></Accepted></ArticleHistory><ArticleCopyright><CopyrightHolderName>Kugler Publications</CopyrightHolderName><CopyrightYear>1995</CopyrightYear></ArticleCopyright><ArticleGrants Type="Regular"><MetadataGrant Grant="OpenAccess"></MetadataGrant><AbstractGrant Grant="OpenAccess"></AbstractGrant><BodyPDFGrant Grant="Restricted"></BodyPDFGrant><BodyHTMLGrant Grant="Restricted"></BodyHTMLGrant><BibliographyGrant Grant="Restricted"></BibliographyGrant><ESMGrant Grant="Restricted"></ESMGrant></ArticleGrants><ArticleContext><JournalID>10695</JournalID><VolumeIDStart>14</VolumeIDStart><VolumeIDEnd>14</VolumeIDEnd><IssueIDStart>4</IssueIDStart><IssueIDEnd>4</IssueIDEnd></ArticleContext></ArticleInfo><ArticleHeader><AuthorGroup><Author AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>B.</GivenName><FamilyName>Cuisset</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff2"><AuthorName DisplayOrder="Western"><GivenName>A.</GivenName><FamilyName>Fostier</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff3"><AuthorName DisplayOrder="Western"><GivenName>P.</GivenName><FamilyName>Williot</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff1 Aff4"><AuthorName DisplayOrder="Western"><GivenName>C.</GivenName><FamilyName>Bennetau-Pelissero</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>F.</GivenName><Particle>Le</Particle><FamilyName>Menn</FamilyName></AuthorName></Author><Affiliation ID="Aff1"><OrgName>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons</OrgName><OrgAddress><Street>Avenue des Facultés</Street><Postcode>33405</Postcode><City>Talence Cedex</City><Country>France</Country></OrgAddress></Affiliation><Affiliation ID="Aff2"><OrgName>Institut National de la Recherche Agronomique, Laboratoire de Physiologie des Poissons, Campus de Beaulieu</OrgName><OrgAddress><Postcode>35042</Postcode><City>Rennes Cedex</City><Country>France</Country></OrgAddress></Affiliation><Affiliation ID="Aff3"><OrgDivision>Division Aquaculture et Pechê</OrgDivision><OrgName>Centre National du Machinisme Agricole, du Génie Rural, des Eaux des Forêts</OrgName><OrgAddress><Street>50 Avenue de Verdun</Street><Postcode>BP 3, 33611</Postcode><City>Gazinet Cedex</City><Country>France</Country></OrgAddress></Affiliation><Affiliation ID="Aff4"><OrgName>ENITA Bordeaux</OrgName><OrgAddress><Postcode>33170</Postcode><City>Gradigham</City><Country>France</Country></OrgAddress></Affiliation></AuthorGroup><Abstract ID="Abs1" Language="En"><Heading>Abstract</Heading><Para>High levels of 11-ketotestosterone (11KT) were found (49 to 160 ng ml<Superscript>−1</Superscript>) in plasma of Siberian sturgeon females during the end of their reproductive cycle. These levels were measured either by specific radioimmunoassay, or both by specific radioimmunoassay and by UV absorption after HPLC (isocratic conditions, 33% methanol, 26% acetonitrile, 41% water). In order to find the origin of 11KT synthesis, ovaries were incubated (30 min and 2h at 20°C) with tritiated 17-hydroxyprogesterone (17OHP) or with tritiated androstenedione (A4). Testosterone (conversion rate from tritiated 17OHP: 4%) and 11-ketotestosterone (conversion rate from tritiated A4: 1.6%) were identified as metabolites of respectively 17OHP and A4 (TLC, HPLC and crystallization). 11β-hydroxyandrostenedione (11βOHA4) and 11β-hydroxytestosterone (11βOHT) were suggested to be intermediate metabolites. Besides interrenal and blood cells were incubated respectively with tritiated cortisol and tritiated A4. 11βOHA4 was identified in interrenal incubation (yield from tritiated cortisol: 1.2%). 11KT in interrenal (yield from tritiated cortisol: 0.14%), and 11βOHA4 and 11KT in blood cells (yield from tritiated A4: 1.6%), were suspected to be synthesized (TLC, HPLC, acetylation). No significant metabolization of tritiated cortisol could be found in liver. The possible contribution of each of these tissues to high 11KT levels found in plasma is discussed.</Para></Abstract><KeywordGroup Language="En"><Heading>Keywords</Heading><Keyword>11KT</Keyword><Keyword>steroidogenesis</Keyword><Keyword>plasma steroids</Keyword><Keyword>ovary</Keyword><Keyword>sturgeon</Keyword><Keyword><Emphasis Type="Italic">Acipenser baeri</Emphasis></Keyword></KeywordGroup><ArticleNote Type="Misc"><SimplePara>To whom correspondence should be sent</SimplePara></ArticleNote></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Occurrence and in vitro biosynthesis of 11-ketotestosterone in Siberian sturgeon, Acipenser baeri Brandt maturing females</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Occurrence and in vitro biosynthesis of 11-ketotestosterone in Siberian sturgeon, Acipenser baeri Brandt maturing females</title></titleInfo><name type="personal"><namePart type="given">B.</namePart><namePart type="family">Cuisset</namePart><affiliation>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A.</namePart><namePart type="family">Fostier</namePart><affiliation>Institut National de la Recherche Agronomique, Laboratoire de Physiologie des Poissons, Campus de Beaulieu, 35042, Rennes Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">P.</namePart><namePart type="family">Williot</namePart><affiliation>Division Aquaculture et Pechê, Centre National du Machinisme Agricole, du Génie Rural, des Eaux des Forêts, 50 Avenue de Verdun, BP 3, 33611, Gazinet Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C.</namePart><namePart type="family">Bennetau-Pelissero</namePart><affiliation>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</affiliation><affiliation>ENITA Bordeaux, 33170, Gradigham, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">F.</namePart><namePart type="family">Le Menn</namePart><affiliation>Université Bordeaux I, U.A.-I.N.R.A. de Biologie de la Reproduction des Poissons, Avenue des Facultés, 33405, Talence Cedex, France</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="OriginalPaper"></genre><originInfo><publisher>Kluwer Academic Publishers</publisher><place><placeTerm type="text">Dordrecht</placeTerm></place><dateIssued encoding="w3cdtf">1995-08-01</dateIssued><copyrightDate encoding="w3cdtf">1995</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Abstract: High levels of 11-ketotestosterone (11KT) were found (49 to 160 ng ml−1) in plasma of Siberian sturgeon females during the end of their reproductive cycle. These levels were measured either by specific radioimmunoassay, or both by specific radioimmunoassay and by UV absorption after HPLC (isocratic conditions, 33% methanol, 26% acetonitrile, 41% water). In order to find the origin of 11KT synthesis, ovaries were incubated (30 min and 2h at 20°C) with tritiated 17-hydroxyprogesterone (17OHP) or with tritiated androstenedione (A4). Testosterone (conversion rate from tritiated 17OHP: 4%) and 11-ketotestosterone (conversion rate from tritiated A4: 1.6%) were identified as metabolites of respectively 17OHP and A4 (TLC, HPLC and crystallization). 11β-hydroxyandrostenedione (11βOHA4) and 11β-hydroxytestosterone (11βOHT) were suggested to be intermediate metabolites. Besides interrenal and blood cells were incubated respectively with tritiated cortisol and tritiated A4. 11βOHA4 was identified in interrenal incubation (yield from tritiated cortisol: 1.2%). 11KT in interrenal (yield from tritiated cortisol: 0.14%), and 11βOHA4 and 11KT in blood cells (yield from tritiated A4: 1.6%), were suspected to be synthesized (TLC, HPLC, acetylation). No significant metabolization of tritiated cortisol could be found in liver. The possible contribution of each of these tissues to high 11KT levels found in plasma is discussed.</abstract><relatedItem type="host"><titleInfo><title>Fish Physiology and Biochemistry</title></titleInfo><titleInfo type="abbreviated"><title>Fish Physiol Biochem</title></titleInfo><genre type="journal" displayLabel="Archive Journal"></genre><originInfo><dateIssued encoding="w3cdtf">1995-08-01</dateIssued><copyrightDate encoding="w3cdtf">1995</copyrightDate></originInfo><subject><genre>Life Sciences</genre><topic>Animal Biochemistry</topic><topic>Hydrobiology</topic><topic>Zoology</topic><topic>Animal Anatomy / Morphology / Histology</topic><topic>Animal Physiology</topic></subject><identifier type="ISSN">0920-1742</identifier><identifier type="eISSN">1573-5168</identifier><identifier type="JournalID">10695</identifier><identifier type="IssueArticleCount">8</identifier><identifier type="VolumeIssueCount">6</identifier><part><date>1995</date><detail type="volume"><number>14</number><caption>vol.</caption></detail><detail type="issue"><number>4</number><caption>no.</caption></detail><extent unit="pages"><start>313</start><end>322</end></extent></part><recordInfo><recordOrigin>Kugler Publications, 1995</recordOrigin></recordInfo></relatedItem><identifier type="istex">89AA26D114C8C03C08AFCAFA40A8CB705CBF6094</identifier><identifier type="DOI">10.1007/BF00004069</identifier><identifier type="ArticleID">BF00004069</identifier><identifier type="ArticleID">Art6</identifier><accessCondition type="use and reproduction" contentType="copyright">Kugler Publications, 1995</accessCondition><recordInfo><recordContentSource>SPRINGER</recordContentSource><recordOrigin>Kugler Publications, 1995</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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