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Desensitization of gonadotropin responses to kisspeptin in the female rat: analyses of LH and FSH secretion at different developmental and metabolic states
1 Department of Cell Biology, Physiology and Immunology, University of Córdoba, Córdoba; 2 Department of Physiology, University of Santiago de Compostela, Santiago de Compostela; and 3 CIBER, Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Córdoba, Spain Submitted 18 Februa...
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Published in: | American journal of physiology: endocrinology and metabolism 2008-06, Vol.294 (6), p.E1088-E1096 |
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creator | Roa, J Vigo, E Garcia-Galiano, D Castellano, J. M Navarro, V. M Pineda, R Dieguez, C Aguilar, E Pinilla, L Tena-Sempere, M |
description | 1 Department of Cell Biology, Physiology and Immunology, University of Córdoba, Córdoba; 2 Department of Physiology, University of Santiago de Compostela, Santiago de Compostela; and 3 CIBER, Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Córdoba, Spain
Submitted 18 February 2008
; accepted in final form 10 April 2008
Kisspeptins have emerged as potent elicitors of gonadotropin secretion and, therefore, putative targets for pharmacological intervention. In this context, desensitization of gonadotropin responses to continuous administration of kisspeptins has begun to be characterized, but information so far available is mostly restricted to LH responses in males, whereas the similar phenomenon in females, of obvious therapeutic interest, remains virtually unexplored. We report herein LH and FSH responses to continuous intracerebral administration of kisspeptin in female rats at different developmental and metabolic states. Infusion of kisspeptin-10 to adult female rats induced a transient elevation in serum LH concentrations, followed by a precipitous drop and normalization of LH levels thereafter. Elevation of LH after kisspeptin infusion was prolonged in underfed animals; a phenomenon mimicked by leptin administration. Conversely, FSH levels were persistently heightened along continuous kisspeptin infusion, but duration of this response was shortened by undernutrition. In pubertal females, LH and FSH levels remained elevated at the end of a 7-day infusion of kisspeptin; responses whose magnitude was augmented by subnutrition but not mimicked by leptin. In all settings, terminal gonadotropin-releasing hormone responses were fully preserved, suggesting that eventual desensitization must occur upstream from the pituitary. In summary, our current data document the pharmacological consequences of continuous administration of kisspeptin to female rats, with remarkable differences being detected between LH and FSH responses, in different developmental and metabolic states. These observations of potential pharmacological interest might help also to delineate the physiological roles of kisspeptins in the dynamic regulation of gonadotropin secretion in the female.
KiSS-1; G protein-coupled receptor 54; gonadotropin-releasing hormone; constant infusion; fasting; leptin; puberty; luteinizing hormone; follicle-stimulating hormone
Address for reprint requests and other correspondence: M. Tena-Sempere, Physiology Section. Dept. of Cell Biolog |
doi_str_mv | 10.1152/ajpendo.90240.2008 |
format | article |
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Submitted 18 February 2008
; accepted in final form 10 April 2008
Kisspeptins have emerged as potent elicitors of gonadotropin secretion and, therefore, putative targets for pharmacological intervention. In this context, desensitization of gonadotropin responses to continuous administration of kisspeptins has begun to be characterized, but information so far available is mostly restricted to LH responses in males, whereas the similar phenomenon in females, of obvious therapeutic interest, remains virtually unexplored. We report herein LH and FSH responses to continuous intracerebral administration of kisspeptin in female rats at different developmental and metabolic states. Infusion of kisspeptin-10 to adult female rats induced a transient elevation in serum LH concentrations, followed by a precipitous drop and normalization of LH levels thereafter. Elevation of LH after kisspeptin infusion was prolonged in underfed animals; a phenomenon mimicked by leptin administration. Conversely, FSH levels were persistently heightened along continuous kisspeptin infusion, but duration of this response was shortened by undernutrition. In pubertal females, LH and FSH levels remained elevated at the end of a 7-day infusion of kisspeptin; responses whose magnitude was augmented by subnutrition but not mimicked by leptin. In all settings, terminal gonadotropin-releasing hormone responses were fully preserved, suggesting that eventual desensitization must occur upstream from the pituitary. In summary, our current data document the pharmacological consequences of continuous administration of kisspeptin to female rats, with remarkable differences being detected between LH and FSH responses, in different developmental and metabolic states. These observations of potential pharmacological interest might help also to delineate the physiological roles of kisspeptins in the dynamic regulation of gonadotropin secretion in the female.
KiSS-1; G protein-coupled receptor 54; gonadotropin-releasing hormone; constant infusion; fasting; leptin; puberty; luteinizing hormone; follicle-stimulating hormone
Address for reprint requests and other correspondence: M. Tena-Sempere, Physiology Section. Dept. of Cell Biology, Physiology and Immunology. Faculty of Medicine, Univ. of Córdoba, Avda. Menéndez Pidal s/n, 14004 Córdoba, Spain (e-mail: fi1tesem{at}uco.es )</description><identifier>ISSN: 0193-1849</identifier><identifier>EISSN: 1522-1555</identifier><identifier>DOI: 10.1152/ajpendo.90240.2008</identifier><identifier>PMID: 18413669</identifier><identifier>CODEN: AJPMD9</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Age Factors ; Animals ; Body Weight - drug effects ; Body Weight - physiology ; Eating - drug effects ; Eating - physiology ; Endocrinology ; Female ; Follicle Stimulating Hormone - secretion ; Hormones ; Kisspeptins ; Leptin - pharmacology ; Luteinizing Hormone - secretion ; Metabolism ; Oligopeptides - pharmacology ; Pharmacology ; Proteins ; Rats ; Rats, Wistar ; Rodents ; Sexual Maturation - drug effects ; Sexual Maturation - physiology</subject><ispartof>American journal of physiology: endocrinology and metabolism, 2008-06, Vol.294 (6), p.E1088-E1096</ispartof><rights>Copyright American Physiological Society Jun 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c449t-434572e62ee3cdaaf7e549d123770e71d27feecc7db8d029e77c837e9a39e1103</citedby><cites>FETCH-LOGICAL-c449t-434572e62ee3cdaaf7e549d123770e71d27feecc7db8d029e77c837e9a39e1103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18413669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roa, J</creatorcontrib><creatorcontrib>Vigo, E</creatorcontrib><creatorcontrib>Garcia-Galiano, D</creatorcontrib><creatorcontrib>Castellano, J. M</creatorcontrib><creatorcontrib>Navarro, V. M</creatorcontrib><creatorcontrib>Pineda, R</creatorcontrib><creatorcontrib>Dieguez, C</creatorcontrib><creatorcontrib>Aguilar, E</creatorcontrib><creatorcontrib>Pinilla, L</creatorcontrib><creatorcontrib>Tena-Sempere, M</creatorcontrib><title>Desensitization of gonadotropin responses to kisspeptin in the female rat: analyses of LH and FSH secretion at different developmental and metabolic states</title><title>American journal of physiology: endocrinology and metabolism</title><addtitle>Am J Physiol Endocrinol Metab</addtitle><description>1 Department of Cell Biology, Physiology and Immunology, University of Córdoba, Córdoba; 2 Department of Physiology, University of Santiago de Compostela, Santiago de Compostela; and 3 CIBER, Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Córdoba, Spain
Submitted 18 February 2008
; accepted in final form 10 April 2008
Kisspeptins have emerged as potent elicitors of gonadotropin secretion and, therefore, putative targets for pharmacological intervention. In this context, desensitization of gonadotropin responses to continuous administration of kisspeptins has begun to be characterized, but information so far available is mostly restricted to LH responses in males, whereas the similar phenomenon in females, of obvious therapeutic interest, remains virtually unexplored. We report herein LH and FSH responses to continuous intracerebral administration of kisspeptin in female rats at different developmental and metabolic states. Infusion of kisspeptin-10 to adult female rats induced a transient elevation in serum LH concentrations, followed by a precipitous drop and normalization of LH levels thereafter. Elevation of LH after kisspeptin infusion was prolonged in underfed animals; a phenomenon mimicked by leptin administration. Conversely, FSH levels were persistently heightened along continuous kisspeptin infusion, but duration of this response was shortened by undernutrition. In pubertal females, LH and FSH levels remained elevated at the end of a 7-day infusion of kisspeptin; responses whose magnitude was augmented by subnutrition but not mimicked by leptin. In all settings, terminal gonadotropin-releasing hormone responses were fully preserved, suggesting that eventual desensitization must occur upstream from the pituitary. In summary, our current data document the pharmacological consequences of continuous administration of kisspeptin to female rats, with remarkable differences being detected between LH and FSH responses, in different developmental and metabolic states. These observations of potential pharmacological interest might help also to delineate the physiological roles of kisspeptins in the dynamic regulation of gonadotropin secretion in the female.
KiSS-1; G protein-coupled receptor 54; gonadotropin-releasing hormone; constant infusion; fasting; leptin; puberty; luteinizing hormone; follicle-stimulating hormone
Address for reprint requests and other correspondence: M. Tena-Sempere, Physiology Section. Dept. of Cell Biology, Physiology and Immunology. Faculty of Medicine, Univ. of Córdoba, Avda. Menéndez Pidal s/n, 14004 Córdoba, Spain (e-mail: fi1tesem{at}uco.es )</description><subject>Age Factors</subject><subject>Animals</subject><subject>Body Weight - drug effects</subject><subject>Body Weight - physiology</subject><subject>Eating - drug effects</subject><subject>Eating - physiology</subject><subject>Endocrinology</subject><subject>Female</subject><subject>Follicle Stimulating Hormone - secretion</subject><subject>Hormones</subject><subject>Kisspeptins</subject><subject>Leptin - pharmacology</subject><subject>Luteinizing Hormone - secretion</subject><subject>Metabolism</subject><subject>Oligopeptides - pharmacology</subject><subject>Pharmacology</subject><subject>Proteins</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Rodents</subject><subject>Sexual Maturation - drug effects</subject><subject>Sexual Maturation - physiology</subject><issn>0193-1849</issn><issn>1522-1555</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkc2O0zAUhSMEYsrAC7BAFgt2Kf5J4nh2aJhSpEosGNaWG9-0Lk5sbAem8yq8LO7PCISEkCzd6-vvHFn3FMVLgueE1PSt2nkYtZsLTCs8pxi3j4pZfqAlqev6cTHDRLCStJW4KJ7FuMMY87qiT4uLPCOsacSs-PkeIozRJHOvknEjcj3auFFpl4LzZkQBondjhIiSQ19NjB58yvN80hZQD4OygIJKV0iNyu4PZPZYLfNVo8XnJYrQBTh6q4S06XsIMOYOvoN1fsi9skd4gKTWzpoOxaQSxOfFk17ZCC_O9bL4sri5vV6Wq08fPl6_W5VdVYlUVqyqOYWGArBOK9VzqCuhCWWcY-BEU94DdB3X61ZjKoDzrmUchGICCMHssnhz8vXBfZsgJjmY2IG1agQ3RclJw1rBxH9Bitua4IZk8PVf4M5NIa8nM4wyXOP64EZPUBdcjAF66YMZVNhLguUhYHkOWB4DloeAs-jV2XlaD6B_S86JZuDqBGzNZvvDBJB-u4_GWbfZy8Vk7S3cpQdnKirZyBuC21Z63Wfx_N_ih9_8IWK_ACmQy1s</recordid><startdate>20080601</startdate><enddate>20080601</enddate><creator>Roa, J</creator><creator>Vigo, E</creator><creator>Garcia-Galiano, D</creator><creator>Castellano, J. M</creator><creator>Navarro, V. M</creator><creator>Pineda, R</creator><creator>Dieguez, C</creator><creator>Aguilar, E</creator><creator>Pinilla, L</creator><creator>Tena-Sempere, M</creator><general>American Physiological Society</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>7QP</scope><scope>7TS</scope><scope>7U7</scope><scope>C1K</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20080601</creationdate><title>Desensitization of gonadotropin responses to kisspeptin in the female rat: analyses of LH and FSH secretion at different developmental and metabolic states</title><author>Roa, J ; Vigo, E ; Garcia-Galiano, D ; Castellano, J. M ; Navarro, V. 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M</creatorcontrib><creatorcontrib>Navarro, V. M</creatorcontrib><creatorcontrib>Pineda, R</creatorcontrib><creatorcontrib>Dieguez, C</creatorcontrib><creatorcontrib>Aguilar, E</creatorcontrib><creatorcontrib>Pinilla, L</creatorcontrib><creatorcontrib>Tena-Sempere, M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology: endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roa, J</au><au>Vigo, E</au><au>Garcia-Galiano, D</au><au>Castellano, J. M</au><au>Navarro, V. M</au><au>Pineda, R</au><au>Dieguez, C</au><au>Aguilar, E</au><au>Pinilla, L</au><au>Tena-Sempere, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Desensitization of gonadotropin responses to kisspeptin in the female rat: analyses of LH and FSH secretion at different developmental and metabolic states</atitle><jtitle>American journal of physiology: endocrinology and metabolism</jtitle><addtitle>Am J Physiol Endocrinol Metab</addtitle><date>2008-06-01</date><risdate>2008</risdate><volume>294</volume><issue>6</issue><spage>E1088</spage><epage>E1096</epage><pages>E1088-E1096</pages><issn>0193-1849</issn><eissn>1522-1555</eissn><coden>AJPMD9</coden><abstract>1 Department of Cell Biology, Physiology and Immunology, University of Córdoba, Córdoba; 2 Department of Physiology, University of Santiago de Compostela, Santiago de Compostela; and 3 CIBER, Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Córdoba, Spain
Submitted 18 February 2008
; accepted in final form 10 April 2008
Kisspeptins have emerged as potent elicitors of gonadotropin secretion and, therefore, putative targets for pharmacological intervention. In this context, desensitization of gonadotropin responses to continuous administration of kisspeptins has begun to be characterized, but information so far available is mostly restricted to LH responses in males, whereas the similar phenomenon in females, of obvious therapeutic interest, remains virtually unexplored. We report herein LH and FSH responses to continuous intracerebral administration of kisspeptin in female rats at different developmental and metabolic states. Infusion of kisspeptin-10 to adult female rats induced a transient elevation in serum LH concentrations, followed by a precipitous drop and normalization of LH levels thereafter. Elevation of LH after kisspeptin infusion was prolonged in underfed animals; a phenomenon mimicked by leptin administration. Conversely, FSH levels were persistently heightened along continuous kisspeptin infusion, but duration of this response was shortened by undernutrition. In pubertal females, LH and FSH levels remained elevated at the end of a 7-day infusion of kisspeptin; responses whose magnitude was augmented by subnutrition but not mimicked by leptin. In all settings, terminal gonadotropin-releasing hormone responses were fully preserved, suggesting that eventual desensitization must occur upstream from the pituitary. In summary, our current data document the pharmacological consequences of continuous administration of kisspeptin to female rats, with remarkable differences being detected between LH and FSH responses, in different developmental and metabolic states. These observations of potential pharmacological interest might help also to delineate the physiological roles of kisspeptins in the dynamic regulation of gonadotropin secretion in the female.
KiSS-1; G protein-coupled receptor 54; gonadotropin-releasing hormone; constant infusion; fasting; leptin; puberty; luteinizing hormone; follicle-stimulating hormone
Address for reprint requests and other correspondence: M. Tena-Sempere, Physiology Section. Dept. of Cell Biology, Physiology and Immunology. Faculty of Medicine, Univ. of Córdoba, Avda. Menéndez Pidal s/n, 14004 Córdoba, Spain (e-mail: fi1tesem{at}uco.es )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>18413669</pmid><doi>10.1152/ajpendo.90240.2008</doi></addata></record> |
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source | American Physiological Society Journals |
subjects | Age Factors Animals Body Weight - drug effects Body Weight - physiology Eating - drug effects Eating - physiology Endocrinology Female Follicle Stimulating Hormone - secretion Hormones Kisspeptins Leptin - pharmacology Luteinizing Hormone - secretion Metabolism Oligopeptides - pharmacology Pharmacology Proteins Rats Rats, Wistar Rodents Sexual Maturation - drug effects Sexual Maturation - physiology |
title | Desensitization of gonadotropin responses to kisspeptin in the female rat: analyses of LH and FSH secretion at different developmental and metabolic states |
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