Melatonin Induces the Expression of Gonadotropin-Inhibitory Hormone in the Avian Brain
We recently identified a novel hypothalamic neuropeptide inhibiting gonadotropin release in quail and termed it gonadotropin-inhibitory hormone (GnIH). Cell bodies and terminals containing the dodecapeptide GnIH are localized in the paraventricular nucleus (PVN) and median eminence, respectively. To...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2005-02, Vol.102 (8), p.3052-3057 |
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creator | Ubuka, Takayoshi Bentley, George E. Ukena, Kazuyoshi Wingfield, John C. Tsutsui, Kazuyoshi McCann, S. M. |
description | We recently identified a novel hypothalamic neuropeptide inhibiting gonadotropin release in quail and termed it gonadotropin-inhibitory hormone (GnIH). Cell bodies and terminals containing the dodecapeptide GnIH are localized in the paraventricular nucleus (PVN) and median eminence, respectively. To understand the physiological role of GnIH, we investigated the mechanisms that regulate GnIH expression. In this study, we show that melatonin originating from the pineal gland and eyes induces GnIH expression in the quail brain. Pinealectomy (Px) combined with orbital enucleation (Ex) (Px plus Ex) decreased the expression of GnIH precursor mRNA and content of mature GnIH peptide in the diencephalon, which includes the PVN and median eminence. Melatonin administration to Px plus Ex birds caused a dose-dependent increase in expression of GnIH precursor mRNA and production of mature peptide. The expression of GnIH was photoperiodically controlled and increased under short-day photoperiods, when the duration of melatonin secretion increases. To identify the mode of melatonin action on GnIH induction, we investigated the expression of Mel1 c, a melatonin receptor sub-type, in GnIH neurons. In situ hybridization of Mel1 cmRNA combined with immunocytochemistry for GnIH revealed that Mel1 cmRNA was expressed in GnIH-immunoreactive neurons in the PVN. Melatonin receptor autoradiography further revealed specific binding of melatonin in the PVN. These results indicate that melatonin is a key factor for GnIH induction. Melatonin appears to act directly on GnIH neurons through its receptor to induce GnIH expression. This is the first demonstration, to our knowledge, of a direct action of melatonin on neuropeptide induction in any vertebrate class. |
doi_str_mv | 10.1073/pnas.0403840102 |
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M.</creator><creatorcontrib>Ubuka, Takayoshi ; Bentley, George E. ; Ukena, Kazuyoshi ; Wingfield, John C. ; Tsutsui, Kazuyoshi ; McCann, S. M.</creatorcontrib><description>We recently identified a novel hypothalamic neuropeptide inhibiting gonadotropin release in quail and termed it gonadotropin-inhibitory hormone (GnIH). Cell bodies and terminals containing the dodecapeptide GnIH are localized in the paraventricular nucleus (PVN) and median eminence, respectively. To understand the physiological role of GnIH, we investigated the mechanisms that regulate GnIH expression. In this study, we show that melatonin originating from the pineal gland and eyes induces GnIH expression in the quail brain. Pinealectomy (Px) combined with orbital enucleation (Ex) (Px plus Ex) decreased the expression of GnIH precursor mRNA and content of mature GnIH peptide in the diencephalon, which includes the PVN and median eminence. Melatonin administration to Px plus Ex birds caused a dose-dependent increase in expression of GnIH precursor mRNA and production of mature peptide. The expression of GnIH was photoperiodically controlled and increased under short-day photoperiods, when the duration of melatonin secretion increases. To identify the mode of melatonin action on GnIH induction, we investigated the expression of Mel1 c, a melatonin receptor sub-type, in GnIH neurons. In situ hybridization of Mel1 cmRNA combined with immunocytochemistry for GnIH revealed that Mel1 cmRNA was expressed in GnIH-immunoreactive neurons in the PVN. Melatonin receptor autoradiography further revealed specific binding of melatonin in the PVN. These results indicate that melatonin is a key factor for GnIH induction. Melatonin appears to act directly on GnIH neurons through its receptor to induce GnIH expression. This is the first demonstration, to our knowledge, of a direct action of melatonin on neuropeptide induction in any vertebrate class.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0403840102</identifier><identifier>PMID: 15708982</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Animals ; Avian Proteins - genetics ; Base Sequence ; Biological Sciences ; Birds ; Brain - drug effects ; Brain - metabolism ; Coturnix ; Coturnix japonica ; Diencephalon ; Gene expression ; Gene Expression Regulation - drug effects ; Hormones ; Hypothalamic Hormones - genetics ; Immunocytochemistry ; In situ hybridization ; Male ; Melatonin - metabolism ; Melatonin - pharmacology ; Melatonin receptors ; Messenger RNA ; Molecular Sequence Data ; Neurology ; Neurons ; Neuropeptides ; Orbit - physiology ; Paraventricular Hypothalamic Nucleus - metabolism ; Peptides ; Photoperiod ; Pineal Gland - physiology ; Quails ; Receptors, Melatonin - genetics ; RNA, Messenger - analysis ; Secretion</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2005-02, Vol.102 (8), p.3052-3057</ispartof><rights>Copyright 1993/2005 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Feb 22, 2005</rights><rights>Copyright © 2005, The National Academy of Sciences 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c590t-f560383936380904a8b030558005365a3994a1baea5e4d6ffba9e2dea01107c53</citedby><cites>FETCH-LOGICAL-c590t-f560383936380904a8b030558005365a3994a1baea5e4d6ffba9e2dea01107c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/102/8.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3374744$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3374744$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,315,728,781,785,804,886,27929,27930,53796,53798,58022,58255</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15708982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ubuka, Takayoshi</creatorcontrib><creatorcontrib>Bentley, George E.</creatorcontrib><creatorcontrib>Ukena, Kazuyoshi</creatorcontrib><creatorcontrib>Wingfield, John C.</creatorcontrib><creatorcontrib>Tsutsui, Kazuyoshi</creatorcontrib><creatorcontrib>McCann, S. M.</creatorcontrib><title>Melatonin Induces the Expression of Gonadotropin-Inhibitory Hormone in the Avian Brain</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>We recently identified a novel hypothalamic neuropeptide inhibiting gonadotropin release in quail and termed it gonadotropin-inhibitory hormone (GnIH). Cell bodies and terminals containing the dodecapeptide GnIH are localized in the paraventricular nucleus (PVN) and median eminence, respectively. To understand the physiological role of GnIH, we investigated the mechanisms that regulate GnIH expression. In this study, we show that melatonin originating from the pineal gland and eyes induces GnIH expression in the quail brain. Pinealectomy (Px) combined with orbital enucleation (Ex) (Px plus Ex) decreased the expression of GnIH precursor mRNA and content of mature GnIH peptide in the diencephalon, which includes the PVN and median eminence. Melatonin administration to Px plus Ex birds caused a dose-dependent increase in expression of GnIH precursor mRNA and production of mature peptide. The expression of GnIH was photoperiodically controlled and increased under short-day photoperiods, when the duration of melatonin secretion increases. To identify the mode of melatonin action on GnIH induction, we investigated the expression of Mel1 c, a melatonin receptor sub-type, in GnIH neurons. In situ hybridization of Mel1 cmRNA combined with immunocytochemistry for GnIH revealed that Mel1 cmRNA was expressed in GnIH-immunoreactive neurons in the PVN. Melatonin receptor autoradiography further revealed specific binding of melatonin in the PVN. These results indicate that melatonin is a key factor for GnIH induction. Melatonin appears to act directly on GnIH neurons through its receptor to induce GnIH expression. This is the first demonstration, to our knowledge, of a direct action of melatonin on neuropeptide induction in any vertebrate class.</description><subject>Animals</subject><subject>Avian Proteins - genetics</subject><subject>Base Sequence</subject><subject>Biological Sciences</subject><subject>Birds</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Coturnix</subject><subject>Coturnix japonica</subject><subject>Diencephalon</subject><subject>Gene expression</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Hormones</subject><subject>Hypothalamic Hormones - genetics</subject><subject>Immunocytochemistry</subject><subject>In situ hybridization</subject><subject>Male</subject><subject>Melatonin - metabolism</subject><subject>Melatonin - pharmacology</subject><subject>Melatonin receptors</subject><subject>Messenger RNA</subject><subject>Molecular Sequence Data</subject><subject>Neurology</subject><subject>Neurons</subject><subject>Neuropeptides</subject><subject>Orbit - physiology</subject><subject>Paraventricular Hypothalamic Nucleus - metabolism</subject><subject>Peptides</subject><subject>Photoperiod</subject><subject>Pineal Gland - physiology</subject><subject>Quails</subject><subject>Receptors, Melatonin - genetics</subject><subject>RNA, Messenger - analysis</subject><subject>Secretion</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkb9v1DAYhi1ERY-WmQWhiAGmtJ9_JfbAUKrSnlTE0na1nMThfMrZwXaq9r_H0Z16LQNMHvw8r77vexF6j-EEQ01PR6fjCTCgggEG8gotMEhcVkzCa7QAIHUpGGGH6G2MawCQXMAbdIh5DUIKskB3P8ygk3fWFUvXTa2JRVqZ4uJhDCZG613h--LSO935FPxoXbl0K9vY5MNjceXDxjtTZHmWzu6tdsW3oK07Rge9HqJ5t3uP0O33i5vzq_L65-Xy_Oy6bLmEVPa8yqNTSSsqQALTogEKPA8JnFZcUymZxo02mhvWVX3faGlIZzTgvH7L6RH6us0dp2Zjuta4FPSgxmA3Ojwqr616-ePsSv3y94ozyWid_c87P_jfk4lJbWxszTBoZ_wUVVWzCipM_gviWgDDZE789Be49lNw-QiKAKaVFGKGTrdQG3yMwfRPE2NQc7FqLlbti83Gx-eL7vldk8-A2dzHESVUPukMfPknoPppGJJ5SJn8sCXXMdf8hFJas5ox-gdw17_G</recordid><startdate>20050222</startdate><enddate>20050222</enddate><creator>Ubuka, Takayoshi</creator><creator>Bentley, George E.</creator><creator>Ukena, Kazuyoshi</creator><creator>Wingfield, John C.</creator><creator>Tsutsui, Kazuyoshi</creator><creator>McCann, S. 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M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Melatonin Induces the Expression of Gonadotropin-Inhibitory Hormone in the Avian Brain</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2005-02-22</date><risdate>2005</risdate><volume>102</volume><issue>8</issue><spage>3052</spage><epage>3057</epage><pages>3052-3057</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>We recently identified a novel hypothalamic neuropeptide inhibiting gonadotropin release in quail and termed it gonadotropin-inhibitory hormone (GnIH). Cell bodies and terminals containing the dodecapeptide GnIH are localized in the paraventricular nucleus (PVN) and median eminence, respectively. To understand the physiological role of GnIH, we investigated the mechanisms that regulate GnIH expression. In this study, we show that melatonin originating from the pineal gland and eyes induces GnIH expression in the quail brain. Pinealectomy (Px) combined with orbital enucleation (Ex) (Px plus Ex) decreased the expression of GnIH precursor mRNA and content of mature GnIH peptide in the diencephalon, which includes the PVN and median eminence. Melatonin administration to Px plus Ex birds caused a dose-dependent increase in expression of GnIH precursor mRNA and production of mature peptide. The expression of GnIH was photoperiodically controlled and increased under short-day photoperiods, when the duration of melatonin secretion increases. To identify the mode of melatonin action on GnIH induction, we investigated the expression of Mel1 c, a melatonin receptor sub-type, in GnIH neurons. In situ hybridization of Mel1 cmRNA combined with immunocytochemistry for GnIH revealed that Mel1 cmRNA was expressed in GnIH-immunoreactive neurons in the PVN. Melatonin receptor autoradiography further revealed specific binding of melatonin in the PVN. These results indicate that melatonin is a key factor for GnIH induction. Melatonin appears to act directly on GnIH neurons through its receptor to induce GnIH expression. This is the first demonstration, to our knowledge, of a direct action of melatonin on neuropeptide induction in any vertebrate class.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>15708982</pmid><doi>10.1073/pnas.0403840102</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Avian Proteins - genetics Base Sequence Biological Sciences Birds Brain - drug effects Brain - metabolism Coturnix Coturnix japonica Diencephalon Gene expression Gene Expression Regulation - drug effects Hormones Hypothalamic Hormones - genetics Immunocytochemistry In situ hybridization Male Melatonin - metabolism Melatonin - pharmacology Melatonin receptors Messenger RNA Molecular Sequence Data Neurology Neurons Neuropeptides Orbit - physiology Paraventricular Hypothalamic Nucleus - metabolism Peptides Photoperiod Pineal Gland - physiology Quails Receptors, Melatonin - genetics RNA, Messenger - analysis Secretion |
title | Melatonin Induces the Expression of Gonadotropin-Inhibitory Hormone in the Avian Brain |
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