Sperm characteristics and androgens in Acipenser ruthenus after induction of spermiation by carp pituitary extract or GnRHa implants.
Identifieur interne : 000430 ( Ncbi/Merge ); précédent : 000429; suivant : 000431Sperm characteristics and androgens in Acipenser ruthenus after induction of spermiation by carp pituitary extract or GnRHa implants.
Auteurs : Sayyed Mohammad Hadi Alavi [République tchèque] ; Azadeh Hatef ; Constantinos C. Mylonas ; David Gela ; Maria Papadaki ; Marek Rodina ; Vojtech Kašpar ; Martin Pšeni Ka ; Peter Podhorec ; Otomar LinhartSource :
- Fish physiology and biochemistry [ 1573-5168 ] ; 2012.
English descriptors
- KwdEn :
- Animals, Drug Implants, Fishes (blood), Fishes (physiology), Gonadotropin-Releasing Hormone (administration & dosage), Gonadotropin-Releasing Hormone (pharmacology), Male, Semen Analysis (veterinary), Sexual Maturation (drug effects), Sperm Motility, Spermatogenesis (drug effects), Spermatogenesis (physiology), Spermatozoa (drug effects), Spermatozoa (physiology), Testosterone (analogs & derivatives), Testosterone (blood), Testosterone (metabolism).
- MESH :
- chemical , administration & dosage : Gonadotropin-Releasing Hormone.
- chemical , analogs & derivatives : Testosterone.
- chemical , blood : Testosterone.
- chemical , metabolism : Testosterone.
- chemical , pharmacology : Gonadotropin-Releasing Hormone.
- chemical : Drug Implants.
- blood : Fishes.
- drug effects : Sexual Maturation, Spermatogenesis, Spermatozoa.
- physiology : Fishes, Spermatogenesis, Spermatozoa.
- veterinary : Semen Analysis.
- Animals, Male, Sperm Motility.
Abstract
Spermiation and changes in androgen (testosterone, T and 11-ketotestosterone, 11-KT) levels were studied in sterlet (Acipenser ruthenus) treated with GnRH agonist implants (DAla(6)-Pro(9)-LHRHa) at 25 and 75 μg kg(-1) b.w. and compared with those males treated with 4 mg kg(-1) b.w. of carp pituitary extract (CPE) and 3 pellets of Ovopel kg(-1) b.w., which contains DAla(6)-Pro(9)NEt-mGnRH and metoclopramide. Sperm quality (sperm mass, spermatozoa concentration and sperm motility and velocity) was evaluated 24, 48 and 72 h after hormonal treatments. Males did not release sperm in the control group injected with physiological solution, while sperm could not be collected 7 days after treatments in all hormonally treated groups. Spermiation rates were 100 % in the CPE and Ovopel groups and 25-50 % in the GnRHa-treated groups. Sperm production was significantly lower in the GnRHa-treated groups than in the CPE and Ovopel groups and decreased 72 h after hormonal treatment. Sperm motility and velocity were higher in the Ovopel and GnRHa (75 μg) groups compared to the CPE and GnRHa (25 μg) groups and decreased 72 h after hormonal treatment. Androgens were only affected in spermiating males and changed in the Ovopel and GnRHa (75 μg) after hormonal treatment. Significant correlations were observed between sperm production, sperm motility and sperm velocity, but not androgens. The present study suggests involvement of dopamine in sturgeon spawning. Additionally, better sperm quality observed in the Ovopel group and particularly sperm motility in the GnRHa (75 μg) suggests enhancement of sperm quality in sturgeon treated with GnRHa. Therefore, further study is needed to induce fully spermiation using GnRHa implants in combination with a dopamine inhibitor.
DOI: 10.1007/s10695-012-9662-9
PubMed: 22665160
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Mylonas</name></author><author><name sortKey="Gela, David" sort="Gela, David" uniqKey="Gela D" first="David" last="Gela">David Gela</name></author><author><name sortKey="Papadaki, Maria" sort="Papadaki, Maria" uniqKey="Papadaki M" first="Maria" last="Papadaki">Maria Papadaki</name></author><author><name sortKey="Rodina, Marek" sort="Rodina, Marek" uniqKey="Rodina M" first="Marek" last="Rodina">Marek Rodina</name></author><author><name sortKey="Kaspar, Vojtech" sort="Kaspar, Vojtech" uniqKey="Kaspar V" first="Vojtech" last="Kašpar">Vojtech Kašpar</name></author><author><name sortKey="Pseni Ka, Martin" sort="Pseni Ka, Martin" uniqKey="Pseni Ka M" first="Martin" last="Pšeni Ka">Martin Pšeni Ka</name></author><author><name sortKey="Podhorec, Peter" sort="Podhorec, Peter" uniqKey="Podhorec P" first="Peter" last="Podhorec">Peter Podhorec</name></author><author><name sortKey="Linhart, Otomar" sort="Linhart, Otomar" uniqKey="Linhart O" first="Otomar" last="Linhart">Otomar Linhart</name></author></analytic><series><title level="j">Fish physiology and biochemistry</title><idno type="eISSN">1573-5168</idno><imprint><date when="2012" type="published">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Drug Implants</term><term>Fishes (blood)</term><term>Fishes (physiology)</term><term>Gonadotropin-Releasing Hormone (administration & dosage)</term><term>Gonadotropin-Releasing Hormone (pharmacology)</term><term>Male</term><term>Semen Analysis (veterinary)</term><term>Sexual Maturation (drug effects)</term><term>Sperm Motility</term><term>Spermatogenesis (drug effects)</term><term>Spermatogenesis (physiology)</term><term>Spermatozoa (drug effects)</term><term>Spermatozoa (physiology)</term><term>Testosterone (analogs & derivatives)</term><term>Testosterone (blood)</term><term>Testosterone (metabolism)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en"><term>Gonadotropin-Releasing Hormone</term></keywords><keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en"><term>Testosterone</term></keywords><keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en"><term>Testosterone</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Testosterone</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Gonadotropin-Releasing Hormone</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Drug Implants</term></keywords><keywords scheme="MESH" qualifier="blood" xml:lang="en"><term>Fishes</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Sexual Maturation</term><term>Spermatogenesis</term><term>Spermatozoa</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Fishes</term><term>Spermatogenesis</term><term>Spermatozoa</term></keywords><keywords scheme="MESH" qualifier="veterinary" xml:lang="en"><term>Semen Analysis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Male</term><term>Sperm Motility</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Spermiation and changes in androgen (testosterone, T and 11-ketotestosterone, 11-KT) levels were studied in sterlet (Acipenser ruthenus) treated with GnRH agonist implants (DAla(6)-Pro(9)-LHRHa) at 25 and 75 μg kg(-1) b.w. and compared with those males treated with 4 mg kg(-1) b.w. of carp pituitary extract (CPE) and 3 pellets of Ovopel kg(-1) b.w., which contains DAla(6)-Pro(9)NEt-mGnRH and metoclopramide. Sperm quality (sperm mass, spermatozoa concentration and sperm motility and velocity) was evaluated 24, 48 and 72 h after hormonal treatments. Males did not release sperm in the control group injected with physiological solution, while sperm could not be collected 7 days after treatments in all hormonally treated groups. Spermiation rates were 100 % in the CPE and Ovopel groups and 25-50 % in the GnRHa-treated groups. Sperm production was significantly lower in the GnRHa-treated groups than in the CPE and Ovopel groups and decreased 72 h after hormonal treatment. Sperm motility and velocity were higher in the Ovopel and GnRHa (75 μg) groups compared to the CPE and GnRHa (25 μg) groups and decreased 72 h after hormonal treatment. Androgens were only affected in spermiating males and changed in the Ovopel and GnRHa (75 μg) after hormonal treatment. Significant correlations were observed between sperm production, sperm motility and sperm velocity, but not androgens. The present study suggests involvement of dopamine in sturgeon spawning. Additionally, better sperm quality observed in the Ovopel group and particularly sperm motility in the GnRHa (75 μg) suggests enhancement of sperm quality in sturgeon treated with GnRHa. Therefore, further study is needed to induce fully spermiation using GnRHa implants in combination with a dopamine inhibitor.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22665160</PMID><DateCreated><Year>2012</Year><Month>11</Month><Day>12</Day></DateCreated><DateCompleted><Year>2013</Year><Month>04</Month><Day>29</Day></DateCompleted><DateRevised><Year>2015</Year><Month>11</Month><Day>19</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1573-5168</ISSN><JournalIssue CitedMedium="Internet"><Volume>38</Volume><Issue>6</Issue><PubDate><Year>2012</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Fish physiology and biochemistry</Title><ISOAbbreviation>Fish Physiol. Biochem.</ISOAbbreviation></Journal><ArticleTitle>Sperm characteristics and androgens in Acipenser ruthenus after induction of spermiation by carp pituitary extract or GnRHa implants.</ArticleTitle><Pagination><MedlinePgn>1655-66</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/s10695-012-9662-9</ELocationID><Abstract><AbstractText>Spermiation and changes in androgen (testosterone, T and 11-ketotestosterone, 11-KT) levels were studied in sterlet (Acipenser ruthenus) treated with GnRH agonist implants (DAla(6)-Pro(9)-LHRHa) at 25 and 75 μg kg(-1) b.w. and compared with those males treated with 4 mg kg(-1) b.w. of carp pituitary extract (CPE) and 3 pellets of Ovopel kg(-1) b.w., which contains DAla(6)-Pro(9)NEt-mGnRH and metoclopramide. Sperm quality (sperm mass, spermatozoa concentration and sperm motility and velocity) was evaluated 24, 48 and 72 h after hormonal treatments. Males did not release sperm in the control group injected with physiological solution, while sperm could not be collected 7 days after treatments in all hormonally treated groups. Spermiation rates were 100 % in the CPE and Ovopel groups and 25-50 % in the GnRHa-treated groups. Sperm production was significantly lower in the GnRHa-treated groups than in the CPE and Ovopel groups and decreased 72 h after hormonal treatment. Sperm motility and velocity were higher in the Ovopel and GnRHa (75 μg) groups compared to the CPE and GnRHa (25 μg) groups and decreased 72 h after hormonal treatment. Androgens were only affected in spermiating males and changed in the Ovopel and GnRHa (75 μg) after hormonal treatment. Significant correlations were observed between sperm production, sperm motility and sperm velocity, but not androgens. The present study suggests involvement of dopamine in sturgeon spawning. Additionally, better sperm quality observed in the Ovopel group and particularly sperm motility in the GnRHa (75 μg) suggests enhancement of sperm quality in sturgeon treated with GnRHa. Therefore, further study is needed to induce fully spermiation using GnRHa implants in combination with a dopamine inhibitor.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Alavi</LastName><ForeName>Sayyed Mohammad Hadi</ForeName><Initials>SM</Initials><AffiliationInfo><Affiliation>South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses, Research Institute of Fish Culture and Hydrobiology, Faculty of Fisheries and Protection of Waters, University of South Bohemia, 389 25 Vodnany, Czech Republic. alavi@frov.jcu.cz</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hatef</LastName><ForeName>Azadeh</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Mylonas</LastName><ForeName>Constantinos C</ForeName><Initials>CC</Initials></Author><Author ValidYN="Y"><LastName>Gela</LastName><ForeName>David</ForeName><Initials>D</Initials></Author><Author ValidYN="Y"><LastName>Papadaki</LastName><ForeName>Maria</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Rodina</LastName><ForeName>Marek</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Kašpar</LastName><ForeName>Vojtech</ForeName><Initials>V</Initials></Author><Author ValidYN="Y"><LastName>Pšenička</LastName><ForeName>Martin</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Podhorec</LastName><ForeName>Peter</ForeName><Initials>P</Initials></Author><Author ValidYN="Y"><LastName>Linhart</LastName><ForeName>Otomar</ForeName><Initials>O</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2012</Year><Month>06</Month><Day>05</Day></ArticleDate></Article><MedlineJournalInfo><Country>Netherlands</Country><MedlineTA>Fish Physiol Biochem</MedlineTA><NlmUniqueID>100955049</NlmUniqueID><ISSNLinking>0920-1742</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D004343">Drug Implants</NameOfSubstance></Chemical><Chemical><RegistryNumber>33515-09-2</RegistryNumber><NameOfSubstance UI="D007987">Gonadotropin-Releasing Hormone</NameOfSubstance></Chemical><Chemical><RegistryNumber>3XMK78S47O</RegistryNumber><NameOfSubstance UI="D013739">Testosterone</NameOfSubstance></Chemical><Chemical><RegistryNumber>KF38W1A85U</RegistryNumber><NameOfSubstance UI="C003600">11-ketotestosterone</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004343" MajorTopicYN="N">Drug Implants</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005399" MajorTopicYN="N">Fishes</DescriptorName><QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007987" MajorTopicYN="N">Gonadotropin-Releasing Hormone</DescriptorName><QualifierName UI="Q000008" MajorTopicYN="N">administration & dosage</QualifierName><QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D055101" MajorTopicYN="N">Semen Analysis</DescriptorName><QualifierName UI="Q000662" MajorTopicYN="N">veterinary</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012741" MajorTopicYN="N">Sexual Maturation</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013081" MajorTopicYN="N">Sperm Motility</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013091" MajorTopicYN="N">Spermatogenesis</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName><QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013094" MajorTopicYN="N">Spermatozoa</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013739" MajorTopicYN="N">Testosterone</DescriptorName><QualifierName UI="Q000031" MajorTopicYN="Y">analogs & derivatives</QualifierName><QualifierName UI="Q000097" MajorTopicYN="N">blood</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2011</Year><Month>12</Month><Day>06</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2012</Year><Month>05</Month><Day>18</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2012</Year><Month>6</Month><Day>6</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2012</Year><Month>6</Month><Day>6</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2013</Year><Month>4</Month><Day>30</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">22665160</ArticleId><ArticleId IdType="doi">10.1007/s10695-012-9662-9</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>République tchèque</li></country></list><tree><noCountry><name sortKey="Gela, David" sort="Gela, David" uniqKey="Gela D" first="David" last="Gela">David Gela</name><name sortKey="Hatef, Azadeh" sort="Hatef, Azadeh" uniqKey="Hatef A" first="Azadeh" last="Hatef">Azadeh Hatef</name><name sortKey="Kaspar, Vojtech" sort="Kaspar, Vojtech" uniqKey="Kaspar V" first="Vojtech" last="Kašpar">Vojtech Kašpar</name><name sortKey="Linhart, Otomar" sort="Linhart, Otomar" uniqKey="Linhart O" first="Otomar" last="Linhart">Otomar Linhart</name><name sortKey="Mylonas, Constantinos C" sort="Mylonas, Constantinos C" uniqKey="Mylonas C" first="Constantinos C" last="Mylonas">Constantinos C. Mylonas</name><name sortKey="Papadaki, Maria" sort="Papadaki, Maria" uniqKey="Papadaki M" first="Maria" last="Papadaki">Maria Papadaki</name><name sortKey="Podhorec, Peter" sort="Podhorec, Peter" uniqKey="Podhorec P" first="Peter" last="Podhorec">Peter Podhorec</name><name sortKey="Pseni Ka, Martin" sort="Pseni Ka, Martin" uniqKey="Pseni Ka M" first="Martin" last="Pšeni Ka">Martin Pšeni Ka</name><name sortKey="Rodina, Marek" sort="Rodina, Marek" uniqKey="Rodina M" first="Marek" last="Rodina">Marek Rodina</name></noCountry><country name="République tchèque"><noRegion><name sortKey="Alavi, Sayyed Mohammad Hadi" sort="Alavi, Sayyed Mohammad Hadi" uniqKey="Alavi S" first="Sayyed Mohammad Hadi" last="Alavi">Sayyed Mohammad Hadi Alavi</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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