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The in Vivo and in Vitro Effects of Exogenous Leptin on Ovulation in the Rat
Abstract Leptin, a hormonal product of the Lep gene, is expressed by adipocytes and is thought to play a role in regulating food intake and reproduction. The leptin protein has been localized in many reproductive tissues, including the ovary. Several publications indicate that the ovary is directly...
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Published in: | Endocrinology (Philadelphia) 2000-06, Vol.141 (6), p.1971-1976 |
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container_end_page | 1976 |
container_issue | 6 |
container_start_page | 1971 |
container_title | Endocrinology (Philadelphia) |
container_volume | 141 |
creator | Duggal, Priya S. Van der Hoek, Kylie H. Milner, Clyde R. Ryan, Natalie K. Armstrong, David T. Magoffin, Denis A. Norman, Robert J. |
description | Abstract
Leptin, a hormonal product of the Lep gene, is expressed by adipocytes and is thought to play a role in regulating food intake and reproduction. The leptin protein has been localized in many reproductive tissues, including the ovary. Several publications indicate that the ovary is directly affected by leptin and that leptin may be a factor linking obesity and reproductive dysfunction. In this study, the effect of systemic leptin administration on ovulation in the rat ovary, both in vivo and in vitro, was investigated. Ip administration of leptin (30 μg at 3 hourly intervals for 15 h) to immature gonadotropin-primed rats caused a decline in ovulation in vivo, from 15.9 ± 2.0 oocytes in the control animals to 5.3 ± 1.6 oocytes in the leptin-treated animals (P < 0.001). Plasma progesterone and estradiol levels were analyzed immediately before ovulation, and neither was altered significantly in animals receiving the leptin treatment. Food consumption and body weight decreased following leptin treatment; however, a loss in body weight alone (pair-fed controls) was insufficient to explain the decrease in ovulation observed in the leptin-treated animals. In vitro perfusion of FSH-primed whole ovaries showed that treatment with leptin in combination with LH significantly decreased ovulations from 5.7 ± 1.6 per ovary perfused with LH alone to 1.3 ± 0.6 in those with LH and 1 μg/ml leptin (P < 0.05). Progesterone and estradiol levels in the samples taken during the perfusion period were unaffected by leptin treatment. In summary, leptin administration resulted in fewer ovulations, both in vivo and in vitro, but did not influence steroid levels. Systemic leptin administration at these doses can therefore inhibit ovulation, a process that occurs through a direct effect on the ovary. |
doi_str_mv | 10.1210/endo.141.6.7509 |
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Leptin, a hormonal product of the Lep gene, is expressed by adipocytes and is thought to play a role in regulating food intake and reproduction. The leptin protein has been localized in many reproductive tissues, including the ovary. Several publications indicate that the ovary is directly affected by leptin and that leptin may be a factor linking obesity and reproductive dysfunction. In this study, the effect of systemic leptin administration on ovulation in the rat ovary, both in vivo and in vitro, was investigated. Ip administration of leptin (30 μg at 3 hourly intervals for 15 h) to immature gonadotropin-primed rats caused a decline in ovulation in vivo, from 15.9 ± 2.0 oocytes in the control animals to 5.3 ± 1.6 oocytes in the leptin-treated animals (P < 0.001). Plasma progesterone and estradiol levels were analyzed immediately before ovulation, and neither was altered significantly in animals receiving the leptin treatment. Food consumption and body weight decreased following leptin treatment; however, a loss in body weight alone (pair-fed controls) was insufficient to explain the decrease in ovulation observed in the leptin-treated animals. In vitro perfusion of FSH-primed whole ovaries showed that treatment with leptin in combination with LH significantly decreased ovulations from 5.7 ± 1.6 per ovary perfused with LH alone to 1.3 ± 0.6 in those with LH and 1 μg/ml leptin (P < 0.05). Progesterone and estradiol levels in the samples taken during the perfusion period were unaffected by leptin treatment. In summary, leptin administration resulted in fewer ovulations, both in vivo and in vitro, but did not influence steroid levels. Systemic leptin administration at these doses can therefore inhibit ovulation, a process that occurs through a direct effect on the ovary.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/endo.141.6.7509</identifier><language>eng</language><publisher>Washington: Oxford University Press</publisher><subject>17β-Estradiol ; Adipocytes ; Animals ; Body weight ; Follicle-stimulating hormone ; Food consumption ; Food intake ; Gametocytes ; Gonadotropins ; In vivo methods and tests ; LEP gene ; Leptin ; Oocytes ; Ovaries ; Ovulation ; Perfusion ; Pituitary (anterior) ; Progesterone ; Sex hormones</subject><ispartof>Endocrinology (Philadelphia), 2000-06, Vol.141 (6), p.1971-1976</ispartof><rights>Copyright © 2000 by The Endocrine Society 2000</rights><rights>Copyright © 2000 by The Endocrine Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2589-35333bff436b9e835d3ce80ccd9a451259b6ee6bcc664a95ec9cfd2accd40bde3</citedby><cites>FETCH-LOGICAL-c2589-35333bff436b9e835d3ce80ccd9a451259b6ee6bcc664a95ec9cfd2accd40bde3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Duggal, Priya S.</creatorcontrib><creatorcontrib>Van der Hoek, Kylie H.</creatorcontrib><creatorcontrib>Milner, Clyde R.</creatorcontrib><creatorcontrib>Ryan, Natalie K.</creatorcontrib><creatorcontrib>Armstrong, David T.</creatorcontrib><creatorcontrib>Magoffin, Denis A.</creatorcontrib><creatorcontrib>Norman, Robert J.</creatorcontrib><title>The in Vivo and in Vitro Effects of Exogenous Leptin on Ovulation in the Rat</title><title>Endocrinology (Philadelphia)</title><description>Abstract
Leptin, a hormonal product of the Lep gene, is expressed by adipocytes and is thought to play a role in regulating food intake and reproduction. The leptin protein has been localized in many reproductive tissues, including the ovary. Several publications indicate that the ovary is directly affected by leptin and that leptin may be a factor linking obesity and reproductive dysfunction. In this study, the effect of systemic leptin administration on ovulation in the rat ovary, both in vivo and in vitro, was investigated. Ip administration of leptin (30 μg at 3 hourly intervals for 15 h) to immature gonadotropin-primed rats caused a decline in ovulation in vivo, from 15.9 ± 2.0 oocytes in the control animals to 5.3 ± 1.6 oocytes in the leptin-treated animals (P < 0.001). Plasma progesterone and estradiol levels were analyzed immediately before ovulation, and neither was altered significantly in animals receiving the leptin treatment. Food consumption and body weight decreased following leptin treatment; however, a loss in body weight alone (pair-fed controls) was insufficient to explain the decrease in ovulation observed in the leptin-treated animals. In vitro perfusion of FSH-primed whole ovaries showed that treatment with leptin in combination with LH significantly decreased ovulations from 5.7 ± 1.6 per ovary perfused with LH alone to 1.3 ± 0.6 in those with LH and 1 μg/ml leptin (P < 0.05). Progesterone and estradiol levels in the samples taken during the perfusion period were unaffected by leptin treatment. In summary, leptin administration resulted in fewer ovulations, both in vivo and in vitro, but did not influence steroid levels. Systemic leptin administration at these doses can therefore inhibit ovulation, a process that occurs through a direct effect on the ovary.</description><subject>17β-Estradiol</subject><subject>Adipocytes</subject><subject>Animals</subject><subject>Body weight</subject><subject>Follicle-stimulating hormone</subject><subject>Food consumption</subject><subject>Food intake</subject><subject>Gametocytes</subject><subject>Gonadotropins</subject><subject>In vivo methods and tests</subject><subject>LEP gene</subject><subject>Leptin</subject><subject>Oocytes</subject><subject>Ovaries</subject><subject>Ovulation</subject><subject>Perfusion</subject><subject>Pituitary (anterior)</subject><subject>Progesterone</subject><subject>Sex hormones</subject><issn>0013-7227</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqFkM9LwzAcxYMoOKdnrwFvQruk-bUcZcwpFAYyvYY0TbRjNjVJh_73ZtS7p-978HnvCw-AW4xKXGG0sH3rS0xxyUvBkDwDMywpKwQW6BzMEMKkEFUlLsFVjPtsKaVkBurdh4VdD9-6o4e6byedgodr56xJEXoH19_-3fZ-jLC2Q8qE7-H2OB506rLKPuWSF52uwYXTh2hv_u4cvD6ud6unot5unlcPdWEqtpQFYYSQxjlKeCPtkrCWGLtExrRSU4YrJhtuLW-M4ZxqyayRxrWVzgBFTWvJHNxNvUPwX6ONSe39GPr8UhFMEMNCYJ6pxUSZ4GMM1qkhdJ86_CiM1GkydZpM5ckUV6fJcuJ-Svhx-Bf-BdnnbIc</recordid><startdate>20000601</startdate><enddate>20000601</enddate><creator>Duggal, Priya S.</creator><creator>Van der Hoek, Kylie H.</creator><creator>Milner, Clyde R.</creator><creator>Ryan, Natalie K.</creator><creator>Armstrong, David T.</creator><creator>Magoffin, Denis A.</creator><creator>Norman, Robert J.</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope></search><sort><creationdate>20000601</creationdate><title>The in Vivo and in Vitro Effects of Exogenous Leptin on Ovulation in the Rat</title><author>Duggal, Priya S. ; Van der Hoek, Kylie H. ; Milner, Clyde R. ; Ryan, Natalie K. ; Armstrong, David T. ; Magoffin, Denis A. ; Norman, Robert J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2589-35333bff436b9e835d3ce80ccd9a451259b6ee6bcc664a95ec9cfd2accd40bde3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>17β-Estradiol</topic><topic>Adipocytes</topic><topic>Animals</topic><topic>Body weight</topic><topic>Follicle-stimulating hormone</topic><topic>Food consumption</topic><topic>Food intake</topic><topic>Gametocytes</topic><topic>Gonadotropins</topic><topic>In vivo methods and tests</topic><topic>LEP gene</topic><topic>Leptin</topic><topic>Oocytes</topic><topic>Ovaries</topic><topic>Ovulation</topic><topic>Perfusion</topic><topic>Pituitary (anterior)</topic><topic>Progesterone</topic><topic>Sex hormones</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duggal, Priya S.</creatorcontrib><creatorcontrib>Van der Hoek, Kylie H.</creatorcontrib><creatorcontrib>Milner, Clyde R.</creatorcontrib><creatorcontrib>Ryan, Natalie K.</creatorcontrib><creatorcontrib>Armstrong, David T.</creatorcontrib><creatorcontrib>Magoffin, Denis A.</creatorcontrib><creatorcontrib>Norman, Robert J.</creatorcontrib><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology 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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duggal, Priya S.</au><au>Van der Hoek, Kylie H.</au><au>Milner, Clyde R.</au><au>Ryan, Natalie K.</au><au>Armstrong, David T.</au><au>Magoffin, Denis A.</au><au>Norman, Robert J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The in Vivo and in Vitro Effects of Exogenous Leptin on Ovulation in the Rat</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><date>2000-06-01</date><risdate>2000</risdate><volume>141</volume><issue>6</issue><spage>1971</spage><epage>1976</epage><pages>1971-1976</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><abstract>Abstract
Leptin, a hormonal product of the Lep gene, is expressed by adipocytes and is thought to play a role in regulating food intake and reproduction. The leptin protein has been localized in many reproductive tissues, including the ovary. Several publications indicate that the ovary is directly affected by leptin and that leptin may be a factor linking obesity and reproductive dysfunction. In this study, the effect of systemic leptin administration on ovulation in the rat ovary, both in vivo and in vitro, was investigated. Ip administration of leptin (30 μg at 3 hourly intervals for 15 h) to immature gonadotropin-primed rats caused a decline in ovulation in vivo, from 15.9 ± 2.0 oocytes in the control animals to 5.3 ± 1.6 oocytes in the leptin-treated animals (P < 0.001). Plasma progesterone and estradiol levels were analyzed immediately before ovulation, and neither was altered significantly in animals receiving the leptin treatment. Food consumption and body weight decreased following leptin treatment; however, a loss in body weight alone (pair-fed controls) was insufficient to explain the decrease in ovulation observed in the leptin-treated animals. In vitro perfusion of FSH-primed whole ovaries showed that treatment with leptin in combination with LH significantly decreased ovulations from 5.7 ± 1.6 per ovary perfused with LH alone to 1.3 ± 0.6 in those with LH and 1 μg/ml leptin (P < 0.05). Progesterone and estradiol levels in the samples taken during the perfusion period were unaffected by leptin treatment. In summary, leptin administration resulted in fewer ovulations, both in vivo and in vitro, but did not influence steroid levels. Systemic leptin administration at these doses can therefore inhibit ovulation, a process that occurs through a direct effect on the ovary.</abstract><cop>Washington</cop><pub>Oxford University Press</pub><doi>10.1210/endo.141.6.7509</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 17β-Estradiol Adipocytes Animals Body weight Follicle-stimulating hormone Food consumption Food intake Gametocytes Gonadotropins In vivo methods and tests LEP gene Leptin Oocytes Ovaries Ovulation Perfusion Pituitary (anterior) Progesterone Sex hormones |
title | The in Vivo and in Vitro Effects of Exogenous Leptin on Ovulation in the Rat |
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