There is Kisspeptin – And Then There is Kisspeptin
While kisspeptin was initially found to function as a metastasis suppressor, after identification of its receptor KISS1R and their expression profiles in tissues such as the hypothalamus and adrenals, kisspeptin and KISS1R were predominantly assigned endocrine functions, including regulating puberty...
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Veröffentlicht in: | Trends in endocrinology and metabolism 2015-10, Vol.26 (10), p.564-572 |
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description | While kisspeptin was initially found to function as a metastasis suppressor, after identification of its receptor KISS1R and their expression profiles in tissues such as the hypothalamus and adrenals, kisspeptin and KISS1R were predominantly assigned endocrine functions, including regulating puberty and fertility through their actions on hypothalamic gonadotropin releasing hormone production. More recently, an alter ego for kisspeptin has emerged, with a significant role in regulating glucose homeostasis, insulin secretion, as well as food intake and body composition, and deficient kisspeptin signaling results in reduced locomotor activity and increased adiposity. This review highlights these recent observations on the role of kisspeptin in metabolism as well as several key questions that need to be addressed in the future. |
doi_str_mv | 10.1016/j.tem.2015.07.008 |
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More recently, an alter ego for kisspeptin has emerged, with a significant role in regulating glucose homeostasis, insulin secretion, as well as food intake and body composition, and deficient kisspeptin signaling results in reduced locomotor activity and increased adiposity. This review highlights these recent observations on the role of kisspeptin in metabolism as well as several key questions that need to be addressed in the future.</description><identifier>ISSN: 1043-2760</identifier><identifier>EISSN: 1879-3061</identifier><identifier>DOI: 10.1016/j.tem.2015.07.008</identifier><identifier>PMID: 26412157</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Animals ; Endocrinology & Metabolism ; Female ; glucagon ; Glucagon - genetics ; Glucagon - metabolism ; Humans ; insulin ; Kisspeptin ; Kisspeptins - genetics ; Kisspeptins - metabolism ; Male ; obesity ; Receptors, G-Protein-Coupled - genetics ; Receptors, G-Protein-Coupled - metabolism ; satiety ; Satiety Response - physiology ; sexual dimorphism</subject><ispartof>Trends in endocrinology and metabolism, 2015-10, Vol.26 (10), p.564-572</ispartof><rights>Elsevier Ltd</rights><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. 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More recently, an alter ego for kisspeptin has emerged, with a significant role in regulating glucose homeostasis, insulin secretion, as well as food intake and body composition, and deficient kisspeptin signaling results in reduced locomotor activity and increased adiposity. This review highlights these recent observations on the role of kisspeptin in metabolism as well as several key questions that need to be addressed in the future.</description><subject>Animals</subject><subject>Endocrinology & Metabolism</subject><subject>Female</subject><subject>glucagon</subject><subject>Glucagon - genetics</subject><subject>Glucagon - metabolism</subject><subject>Humans</subject><subject>insulin</subject><subject>Kisspeptin</subject><subject>Kisspeptins - genetics</subject><subject>Kisspeptins - metabolism</subject><subject>Male</subject><subject>obesity</subject><subject>Receptors, G-Protein-Coupled - genetics</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>satiety</subject><subject>Satiety Response - physiology</subject><subject>sexual dimorphism</subject><issn>1043-2760</issn><issn>1879-3061</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1TAQhS0EoqXwAGxQlmwSPHb8EyFVqir-RCUWlPUosSfUl1znYudW6o534A15EhzdUgFCrMbSnHPG-g5jT4E3wEG_2DQLbRvBQTXcNJzbe-wYrOlqyTXcL2_eyloYzY_Yo5w3nENrQT1kR0K3IECZY9ZeXlGiKuTqfch5R7slxOrHt-_VWfRV2cXqH4LH7MHYT5me3M4T9un1q8vzt_XFhzfvzs8uaqe4XmqvRkW99NY4GpzSw-CtU67rOqVtz601RnAvrRRqAOX4MBg7ekNCj34cWy1P2Okhd7cftuQdxSX1E-5S2PbpBuc-4J-bGK7w83yNrbJGdrIEPL8NSPPXPeUFtyE7mqY-0rzPCAZMa0TXrlI4SF2ac0403p0Bjitt3GChjStt5AYL7eJ59vv_7hy_8BbBy4OACqXrQAmzCxQd-ZDILejn8N_407_cbgoxuH76QjeUN_M-xYIfAbNAjh_Xute2Qa1NA8ifumylmQ</recordid><startdate>20151001</startdate><enddate>20151001</enddate><creator>Hussain, Mehboob A</creator><creator>Song, Woo-Jin</creator><creator>Wolfe, Andrew</creator><general>Elsevier Ltd</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>5PM</scope></search><sort><creationdate>20151001</creationdate><title>There is Kisspeptin – And Then There is Kisspeptin</title><author>Hussain, Mehboob A ; Song, Woo-Jin ; Wolfe, Andrew</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-d5f5ea3d87cebc56bbd8c5c999568a0887720d38325b15c0bb78fd7e26fdff463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Endocrinology & Metabolism</topic><topic>Female</topic><topic>glucagon</topic><topic>Glucagon - genetics</topic><topic>Glucagon - metabolism</topic><topic>Humans</topic><topic>insulin</topic><topic>Kisspeptin</topic><topic>Kisspeptins - genetics</topic><topic>Kisspeptins - metabolism</topic><topic>Male</topic><topic>obesity</topic><topic>Receptors, G-Protein-Coupled - genetics</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>satiety</topic><topic>Satiety Response - physiology</topic><topic>sexual dimorphism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hussain, Mehboob A</creatorcontrib><creatorcontrib>Song, Woo-Jin</creatorcontrib><creatorcontrib>Wolfe, Andrew</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>PubMed Central (Full Participant titles)</collection><jtitle>Trends in endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hussain, Mehboob A</au><au>Song, Woo-Jin</au><au>Wolfe, Andrew</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>There is Kisspeptin – And Then There is Kisspeptin</atitle><jtitle>Trends in endocrinology and metabolism</jtitle><addtitle>Trends Endocrinol Metab</addtitle><date>2015-10-01</date><risdate>2015</risdate><volume>26</volume><issue>10</issue><spage>564</spage><epage>572</epage><pages>564-572</pages><issn>1043-2760</issn><eissn>1879-3061</eissn><abstract>While kisspeptin was initially found to function as a metastasis suppressor, after identification of its receptor KISS1R and their expression profiles in tissues such as the hypothalamus and adrenals, kisspeptin and KISS1R were predominantly assigned endocrine functions, including regulating puberty and fertility through their actions on hypothalamic gonadotropin releasing hormone production. 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subjects | Animals Endocrinology & Metabolism Female glucagon Glucagon - genetics Glucagon - metabolism Humans insulin Kisspeptin Kisspeptins - genetics Kisspeptins - metabolism Male obesity Receptors, G-Protein-Coupled - genetics Receptors, G-Protein-Coupled - metabolism satiety Satiety Response - physiology sexual dimorphism |
title | There is Kisspeptin – And Then There is Kisspeptin |
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