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Kisspeptin neurons mediate reflex ovulation in the musk shrew (Suncus murinus)
The present study investigated whether kisspeptin–G protein-coupled receptor 54 (GPR54) signaling plays a role in mediating mating-induced ovulation in the musk shrew (Suncus murinus), a reflex ovulator. For this purpose, we cloned suncus Kiss1 and Gpr54 cDNA from the hypothalamus and found that sun...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2011-10, Vol.108 (42), p.17527-17532 |
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creator | Inoue, Naoko Sasagawa, Karin Ikai, Kotaro Sasaki, Yuki Tomikawa, Junko Oishi, Shinya Fujii, Nobutaka Uenoyama, Yoshihisa Ohmori, Yasushige Yamamoto, Naoyuki Hondo, Eiichi Maeda, Kei-ichiro Tsukamura, Hiroko |
description | The present study investigated whether kisspeptin–G protein-coupled receptor 54 (GPR54) signaling plays a role in mediating mating-induced ovulation in the musk shrew (Suncus murinus), a reflex ovulator. For this purpose, we cloned suncus Kiss1 and Gpr54 cDNA from the hypothalamus and found that suncus kisspeptin (sKp) consists of 29 amino acid residues (sKp-29). Injection of exogenous sKp-29 mimicked the mating stimulus to induce follicular maturation and ovulation. Administration of several kisspeptins and GPR54 agonists also induced presumed ovulation in a dose-dependent manner, and Gpr54 mRNA was distributed in the hypothalamus, showing that kisspeptins induce ovulation through binding to GPR54. The sKp-29–induced ovulation was blocked completely by pretreatment with a gonadotropin-releasing hormone (GnRH) antagonist, suggesting that kisspeptin activates GnRH neurons to induce ovulation in the musk shrew. In addition, in situ hybridization revealed that Kiss1-expressing cells are located in the medial preoptic area (POA) and arcuate nucleus in the musk shrew hypothalamus. The number of Kiss1-expressing cells in the POA or arcuate nucleus was up-regulated or down-regulated by estradiol, suggesting that kisspeptin neurons in these regions were the targets of the estrogen feedback action. Finally, mating stimulus largely induced c-Fos expression in Kiss1-positive cells in the POA, indicating that the mating stimulus activates POA kisspeptin neurons to induce ovulation. Taken together, these results indicate that kisspeptin–GPR54 signaling plays a role in the induction of ovulation in the musk shrew, a reflex ovulator, as it does in spontaneous ovulators. |
doi_str_mv | 10.1073/pnas.1113035108 |
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fullrecord | <record><control><sourceid>jstor_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1663559455</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>41352537</jstor_id><sourcerecordid>41352537</sourcerecordid><originalsourceid>FETCH-LOGICAL-c622t-96005314bd10536270a71aa3e0678c132a9c2a66c61b59b1aa3584a187db5bf23</originalsourceid><addsrcrecordid>eNqFkTtvFDEUhS0EIkugpgJGVKGY5F6_p0FCES8RQRFSW55Zb3aWWXtijwP8ezzaZQM0VLc43z33cQh5inCKoNjZ6G06RUQGTCDoe2SB0GAteQP3yQKAqlpzyo_Io5Q2ANAIDQ_JEcVGK416QT5_6lMa3Tj1vvIux-BTtXXL3k6uim41uB9VuM2Dnfrgq8JMa1dtc_pWpXV036uTy-y7XFpy7H1Orx6TBys7JPdkX4_J1bu3X88_1Bdf3n88f3NRd5LSqW4kgGDI2yWWKqkCq9Ba5kAq3SGjtumolbKT2IqmnSWhuUWtlq1oV5Qdk9c73zG3Zd3O-SnawYyx39r40wTbm78V36_Ndbg1rFzO-GxwsjeI4Sa7NJltnzo3DNa7kJNBKZkQDRfi_yg0jDPUOLu-_AfdhBx9-YRpyve1olIV6GwHdTGkVJ58WBvBzKmaOVVzl2rpeP7ntQf-d4wFqPbA3Hlnpw2nBpWg89RnO2STphAPDEcmqGCz_mKnr2ww9jr2yVxdUkAOgFpKztgvwWy6Vw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>900087267</pqid></control><display><type>article</type><title>Kisspeptin neurons mediate reflex ovulation in the musk shrew (Suncus murinus)</title><source>JSTOR Archival Journals and Primary Sources Collection</source><source>PubMed Central</source><creator>Inoue, Naoko ; Sasagawa, Karin ; Ikai, Kotaro ; Sasaki, Yuki ; Tomikawa, Junko ; Oishi, Shinya ; Fujii, Nobutaka ; Uenoyama, Yoshihisa ; Ohmori, Yasushige ; Yamamoto, Naoyuki ; Hondo, Eiichi ; Maeda, Kei-ichiro ; Tsukamura, Hiroko</creator><creatorcontrib>Inoue, Naoko ; Sasagawa, Karin ; Ikai, Kotaro ; Sasaki, Yuki ; Tomikawa, Junko ; Oishi, Shinya ; Fujii, Nobutaka ; Uenoyama, Yoshihisa ; Ohmori, Yasushige ; Yamamoto, Naoyuki ; Hondo, Eiichi ; Maeda, Kei-ichiro ; Tsukamura, Hiroko</creatorcontrib><description>The present study investigated whether kisspeptin–G protein-coupled receptor 54 (GPR54) signaling plays a role in mediating mating-induced ovulation in the musk shrew (Suncus murinus), a reflex ovulator. For this purpose, we cloned suncus Kiss1 and Gpr54 cDNA from the hypothalamus and found that suncus kisspeptin (sKp) consists of 29 amino acid residues (sKp-29). Injection of exogenous sKp-29 mimicked the mating stimulus to induce follicular maturation and ovulation. Administration of several kisspeptins and GPR54 agonists also induced presumed ovulation in a dose-dependent manner, and Gpr54 mRNA was distributed in the hypothalamus, showing that kisspeptins induce ovulation through binding to GPR54. The sKp-29–induced ovulation was blocked completely by pretreatment with a gonadotropin-releasing hormone (GnRH) antagonist, suggesting that kisspeptin activates GnRH neurons to induce ovulation in the musk shrew. In addition, in situ hybridization revealed that Kiss1-expressing cells are located in the medial preoptic area (POA) and arcuate nucleus in the musk shrew hypothalamus. The number of Kiss1-expressing cells in the POA or arcuate nucleus was up-regulated or down-regulated by estradiol, suggesting that kisspeptin neurons in these regions were the targets of the estrogen feedback action. Finally, mating stimulus largely induced c-Fos expression in Kiss1-positive cells in the POA, indicating that the mating stimulus activates POA kisspeptin neurons to induce ovulation. Taken together, these results indicate that kisspeptin–GPR54 signaling plays a role in the induction of ovulation in the musk shrew, a reflex ovulator, as it does in spontaneous ovulators.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1113035108</identifier><identifier>PMID: 21987818</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>agonists ; Amino Acid Sequence ; Amino acids ; Animals ; antagonists ; Arcuate nucleus ; Arcuate Nucleus of Hypothalamus - drug effects ; Arcuate Nucleus of Hypothalamus - physiology ; Base Sequence ; Biological Sciences ; Brain ; c-Fos protein ; Cells ; Complementary DNA ; Copulation - physiology ; Corpus Luteum - physiology ; DNA, Complementary - genetics ; Estradiol ; Estradiol - pharmacology ; Estrogens ; Feedback ; Female ; Gene Expression - drug effects ; Gonadotropin-releasing hormone ; Gonadotropin-Releasing Hormone - physiology ; Hormonal regulation ; Hybridization ; in situ hybridization ; Kiss1 protein ; Kisspeptins - genetics ; Kisspeptins - physiology ; Male ; Mating ; Mating behavior ; Messenger RNA ; Molecular Sequence Data ; mRNA ; Neurons ; Ovarian Follicle - physiology ; Ovaries ; Ovulation ; Ovulation - genetics ; Ovulation - physiology ; Phylogeny ; Preoptic area ; Preoptic Area - drug effects ; Preoptic Area - physiology ; Proteins ; Rats ; Receptors, G-Protein-Coupled - genetics ; Receptors, G-Protein-Coupled - physiology ; Reflexes ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Rodents ; Sequence Homology, Amino Acid ; Shrews ; Shrews - physiology ; Suncus ; Suncus murinus ; Tissue Distribution</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2011-10, Vol.108 (42), p.17527-17532</ispartof><rights>copyright © 1993-2008 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Oct 18, 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c622t-96005314bd10536270a71aa3e0678c132a9c2a66c61b59b1aa3584a187db5bf23</citedby><cites>FETCH-LOGICAL-c622t-96005314bd10536270a71aa3e0678c132a9c2a66c61b59b1aa3584a187db5bf23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/108/42.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/41352537$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/41352537$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768,58213,58446</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21987818$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Inoue, Naoko</creatorcontrib><creatorcontrib>Sasagawa, Karin</creatorcontrib><creatorcontrib>Ikai, Kotaro</creatorcontrib><creatorcontrib>Sasaki, Yuki</creatorcontrib><creatorcontrib>Tomikawa, Junko</creatorcontrib><creatorcontrib>Oishi, Shinya</creatorcontrib><creatorcontrib>Fujii, Nobutaka</creatorcontrib><creatorcontrib>Uenoyama, Yoshihisa</creatorcontrib><creatorcontrib>Ohmori, Yasushige</creatorcontrib><creatorcontrib>Yamamoto, Naoyuki</creatorcontrib><creatorcontrib>Hondo, Eiichi</creatorcontrib><creatorcontrib>Maeda, Kei-ichiro</creatorcontrib><creatorcontrib>Tsukamura, Hiroko</creatorcontrib><title>Kisspeptin neurons mediate reflex ovulation in the musk shrew (Suncus murinus)</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The present study investigated whether kisspeptin–G protein-coupled receptor 54 (GPR54) signaling plays a role in mediating mating-induced ovulation in the musk shrew (Suncus murinus), a reflex ovulator. For this purpose, we cloned suncus Kiss1 and Gpr54 cDNA from the hypothalamus and found that suncus kisspeptin (sKp) consists of 29 amino acid residues (sKp-29). Injection of exogenous sKp-29 mimicked the mating stimulus to induce follicular maturation and ovulation. Administration of several kisspeptins and GPR54 agonists also induced presumed ovulation in a dose-dependent manner, and Gpr54 mRNA was distributed in the hypothalamus, showing that kisspeptins induce ovulation through binding to GPR54. The sKp-29–induced ovulation was blocked completely by pretreatment with a gonadotropin-releasing hormone (GnRH) antagonist, suggesting that kisspeptin activates GnRH neurons to induce ovulation in the musk shrew. In addition, in situ hybridization revealed that Kiss1-expressing cells are located in the medial preoptic area (POA) and arcuate nucleus in the musk shrew hypothalamus. The number of Kiss1-expressing cells in the POA or arcuate nucleus was up-regulated or down-regulated by estradiol, suggesting that kisspeptin neurons in these regions were the targets of the estrogen feedback action. Finally, mating stimulus largely induced c-Fos expression in Kiss1-positive cells in the POA, indicating that the mating stimulus activates POA kisspeptin neurons to induce ovulation. Taken together, these results indicate that kisspeptin–GPR54 signaling plays a role in the induction of ovulation in the musk shrew, a reflex ovulator, as it does in spontaneous ovulators.</description><subject>agonists</subject><subject>Amino Acid Sequence</subject><subject>Amino acids</subject><subject>Animals</subject><subject>antagonists</subject><subject>Arcuate nucleus</subject><subject>Arcuate Nucleus of Hypothalamus - drug effects</subject><subject>Arcuate Nucleus of Hypothalamus - physiology</subject><subject>Base Sequence</subject><subject>Biological Sciences</subject><subject>Brain</subject><subject>c-Fos protein</subject><subject>Cells</subject><subject>Complementary DNA</subject><subject>Copulation - physiology</subject><subject>Corpus Luteum - physiology</subject><subject>DNA, Complementary - genetics</subject><subject>Estradiol</subject><subject>Estradiol - pharmacology</subject><subject>Estrogens</subject><subject>Feedback</subject><subject>Female</subject><subject>Gene Expression - drug effects</subject><subject>Gonadotropin-releasing hormone</subject><subject>Gonadotropin-Releasing Hormone - physiology</subject><subject>Hormonal regulation</subject><subject>Hybridization</subject><subject>in situ hybridization</subject><subject>Kiss1 protein</subject><subject>Kisspeptins - genetics</subject><subject>Kisspeptins - physiology</subject><subject>Male</subject><subject>Mating</subject><subject>Mating behavior</subject><subject>Messenger RNA</subject><subject>Molecular Sequence Data</subject><subject>mRNA</subject><subject>Neurons</subject><subject>Ovarian Follicle - physiology</subject><subject>Ovaries</subject><subject>Ovulation</subject><subject>Ovulation - genetics</subject><subject>Ovulation - physiology</subject><subject>Phylogeny</subject><subject>Preoptic area</subject><subject>Preoptic Area - drug effects</subject><subject>Preoptic Area - physiology</subject><subject>Proteins</subject><subject>Rats</subject><subject>Receptors, G-Protein-Coupled - genetics</subject><subject>Receptors, G-Protein-Coupled - physiology</subject><subject>Reflexes</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Rodents</subject><subject>Sequence Homology, Amino Acid</subject><subject>Shrews</subject><subject>Shrews - physiology</subject><subject>Suncus</subject><subject>Suncus murinus</subject><subject>Tissue Distribution</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkTtvFDEUhS0EIkugpgJGVKGY5F6_p0FCES8RQRFSW55Zb3aWWXtijwP8ezzaZQM0VLc43z33cQh5inCKoNjZ6G06RUQGTCDoe2SB0GAteQP3yQKAqlpzyo_Io5Q2ANAIDQ_JEcVGK416QT5_6lMa3Tj1vvIux-BTtXXL3k6uim41uB9VuM2Dnfrgq8JMa1dtc_pWpXV036uTy-y7XFpy7H1Orx6TBys7JPdkX4_J1bu3X88_1Bdf3n88f3NRd5LSqW4kgGDI2yWWKqkCq9Ba5kAq3SGjtumolbKT2IqmnSWhuUWtlq1oV5Qdk9c73zG3Zd3O-SnawYyx39r40wTbm78V36_Ndbg1rFzO-GxwsjeI4Sa7NJltnzo3DNa7kJNBKZkQDRfi_yg0jDPUOLu-_AfdhBx9-YRpyve1olIV6GwHdTGkVJ58WBvBzKmaOVVzl2rpeP7ntQf-d4wFqPbA3Hlnpw2nBpWg89RnO2STphAPDEcmqGCz_mKnr2ww9jr2yVxdUkAOgFpKztgvwWy6Vw</recordid><startdate>20111018</startdate><enddate>20111018</enddate><creator>Inoue, Naoko</creator><creator>Sasagawa, Karin</creator><creator>Ikai, Kotaro</creator><creator>Sasaki, Yuki</creator><creator>Tomikawa, Junko</creator><creator>Oishi, Shinya</creator><creator>Fujii, Nobutaka</creator><creator>Uenoyama, Yoshihisa</creator><creator>Ohmori, Yasushige</creator><creator>Yamamoto, Naoyuki</creator><creator>Hondo, Eiichi</creator><creator>Maeda, Kei-ichiro</creator><creator>Tsukamura, Hiroko</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</scope><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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20111018</creationdate><title>Kisspeptin neurons mediate reflex ovulation in the musk shrew (Suncus murinus)</title><author>Inoue, Naoko ; Sasagawa, Karin ; Ikai, Kotaro ; Sasaki, Yuki ; Tomikawa, Junko ; Oishi, Shinya ; Fujii, Nobutaka ; Uenoyama, Yoshihisa ; Ohmori, Yasushige ; Yamamoto, Naoyuki ; Hondo, Eiichi ; Maeda, Kei-ichiro ; Tsukamura, Hiroko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c622t-96005314bd10536270a71aa3e0678c132a9c2a66c61b59b1aa3584a187db5bf23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>agonists</topic><topic>Amino Acid Sequence</topic><topic>Amino acids</topic><topic>Animals</topic><topic>antagonists</topic><topic>Arcuate nucleus</topic><topic>Arcuate Nucleus of Hypothalamus - drug effects</topic><topic>Arcuate Nucleus of Hypothalamus - physiology</topic><topic>Base Sequence</topic><topic>Biological Sciences</topic><topic>Brain</topic><topic>c-Fos protein</topic><topic>Cells</topic><topic>Complementary DNA</topic><topic>Copulation - physiology</topic><topic>Corpus Luteum - physiology</topic><topic>DNA, Complementary - genetics</topic><topic>Estradiol</topic><topic>Estradiol - pharmacology</topic><topic>Estrogens</topic><topic>Feedback</topic><topic>Female</topic><topic>Gene Expression - drug effects</topic><topic>Gonadotropin-releasing hormone</topic><topic>Gonadotropin-Releasing Hormone - physiology</topic><topic>Hormonal regulation</topic><topic>Hybridization</topic><topic>in situ hybridization</topic><topic>Kiss1 protein</topic><topic>Kisspeptins - genetics</topic><topic>Kisspeptins - physiology</topic><topic>Male</topic><topic>Mating</topic><topic>Mating behavior</topic><topic>Messenger RNA</topic><topic>Molecular Sequence Data</topic><topic>mRNA</topic><topic>Neurons</topic><topic>Ovarian Follicle - physiology</topic><topic>Ovaries</topic><topic>Ovulation</topic><topic>Ovulation - genetics</topic><topic>Ovulation - physiology</topic><topic>Phylogeny</topic><topic>Preoptic area</topic><topic>Preoptic Area - drug effects</topic><topic>Preoptic Area - physiology</topic><topic>Proteins</topic><topic>Rats</topic><topic>Receptors, G-Protein-Coupled - genetics</topic><topic>Receptors, G-Protein-Coupled - physiology</topic><topic>Reflexes</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Rodents</topic><topic>Sequence Homology, Amino Acid</topic><topic>Shrews</topic><topic>Shrews - physiology</topic><topic>Suncus</topic><topic>Suncus murinus</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Inoue, Naoko</creatorcontrib><creatorcontrib>Sasagawa, Karin</creatorcontrib><creatorcontrib>Ikai, Kotaro</creatorcontrib><creatorcontrib>Sasaki, Yuki</creatorcontrib><creatorcontrib>Tomikawa, Junko</creatorcontrib><creatorcontrib>Oishi, Shinya</creatorcontrib><creatorcontrib>Fujii, Nobutaka</creatorcontrib><creatorcontrib>Uenoyama, Yoshihisa</creatorcontrib><creatorcontrib>Ohmori, Yasushige</creatorcontrib><creatorcontrib>Yamamoto, Naoyuki</creatorcontrib><creatorcontrib>Hondo, Eiichi</creatorcontrib><creatorcontrib>Maeda, Kei-ichiro</creatorcontrib><creatorcontrib>Tsukamura, Hiroko</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Inoue, Naoko</au><au>Sasagawa, Karin</au><au>Ikai, Kotaro</au><au>Sasaki, Yuki</au><au>Tomikawa, Junko</au><au>Oishi, Shinya</au><au>Fujii, Nobutaka</au><au>Uenoyama, Yoshihisa</au><au>Ohmori, Yasushige</au><au>Yamamoto, Naoyuki</au><au>Hondo, Eiichi</au><au>Maeda, Kei-ichiro</au><au>Tsukamura, Hiroko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kisspeptin neurons mediate reflex ovulation in the musk shrew (Suncus murinus)</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2011-10-18</date><risdate>2011</risdate><volume>108</volume><issue>42</issue><spage>17527</spage><epage>17532</epage><pages>17527-17532</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>The present study investigated whether kisspeptin–G protein-coupled receptor 54 (GPR54) signaling plays a role in mediating mating-induced ovulation in the musk shrew (Suncus murinus), a reflex ovulator. For this purpose, we cloned suncus Kiss1 and Gpr54 cDNA from the hypothalamus and found that suncus kisspeptin (sKp) consists of 29 amino acid residues (sKp-29). Injection of exogenous sKp-29 mimicked the mating stimulus to induce follicular maturation and ovulation. Administration of several kisspeptins and GPR54 agonists also induced presumed ovulation in a dose-dependent manner, and Gpr54 mRNA was distributed in the hypothalamus, showing that kisspeptins induce ovulation through binding to GPR54. The sKp-29–induced ovulation was blocked completely by pretreatment with a gonadotropin-releasing hormone (GnRH) antagonist, suggesting that kisspeptin activates GnRH neurons to induce ovulation in the musk shrew. In addition, in situ hybridization revealed that Kiss1-expressing cells are located in the medial preoptic area (POA) and arcuate nucleus in the musk shrew hypothalamus. The number of Kiss1-expressing cells in the POA or arcuate nucleus was up-regulated or down-regulated by estradiol, suggesting that kisspeptin neurons in these regions were the targets of the estrogen feedback action. Finally, mating stimulus largely induced c-Fos expression in Kiss1-positive cells in the POA, indicating that the mating stimulus activates POA kisspeptin neurons to induce ovulation. Taken together, these results indicate that kisspeptin–GPR54 signaling plays a role in the induction of ovulation in the musk shrew, a reflex ovulator, as it does in spontaneous ovulators.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>21987818</pmid><doi>10.1073/pnas.1113035108</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | agonists Amino Acid Sequence Amino acids Animals antagonists Arcuate nucleus Arcuate Nucleus of Hypothalamus - drug effects Arcuate Nucleus of Hypothalamus - physiology Base Sequence Biological Sciences Brain c-Fos protein Cells Complementary DNA Copulation - physiology Corpus Luteum - physiology DNA, Complementary - genetics Estradiol Estradiol - pharmacology Estrogens Feedback Female Gene Expression - drug effects Gonadotropin-releasing hormone Gonadotropin-Releasing Hormone - physiology Hormonal regulation Hybridization in situ hybridization Kiss1 protein Kisspeptins - genetics Kisspeptins - physiology Male Mating Mating behavior Messenger RNA Molecular Sequence Data mRNA Neurons Ovarian Follicle - physiology Ovaries Ovulation Ovulation - genetics Ovulation - physiology Phylogeny Preoptic area Preoptic Area - drug effects Preoptic Area - physiology Proteins Rats Receptors, G-Protein-Coupled - genetics Receptors, G-Protein-Coupled - physiology Reflexes RNA, Messenger - genetics RNA, Messenger - metabolism Rodents Sequence Homology, Amino Acid Shrews Shrews - physiology Suncus Suncus murinus Tissue Distribution |
title | Kisspeptin neurons mediate reflex ovulation in the musk shrew (Suncus murinus) |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T20%3A43%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Kisspeptin%20neurons%20mediate%20reflex%20ovulation%20in%20the%20musk%20shrew%20(Suncus%20murinus)&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20-%20PNAS&rft.au=Inoue,%20Naoko&rft.date=2011-10-18&rft.volume=108&rft.issue=42&rft.spage=17527&rft.epage=17532&rft.pages=17527-17532&rft.issn=0027-8424&rft.eissn=1091-6490&rft_id=info:doi/10.1073/pnas.1113035108&rft_dat=%3Cjstor_proqu%3E41352537%3C/jstor_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c622t-96005314bd10536270a71aa3e0678c132a9c2a66c61b59b1aa3584a187db5bf23%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=900087267&rft_id=info:pmid/21987818&rft_jstor_id=41352537&rfr_iscdi=true |