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Leptin Within the Subphysiological to Physiological Range Dose Dependently Improves Male Reproductive Function in an Obesity Mouse Model
Obesity has recently been linked with reduced fertility, and the mechanisms underpinning this effect are currently unknown. The adipokine leptin is dysregulated in obesity and affects reproductive tracts; therefore, we investigated the dose-dependent effects of leptin on Leydig cell function and spe...
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Published in: | Endocrinology (Philadelphia) 2016-06, Vol.157 (6), p.2461-2468 |
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creator | Hoffmann, Annett Manjowk, Gloria-Maria Wagner, Isabel Viola Klöting, Nora Ebert, Thomas Jessnitzer, Beate Lössner, Ulrike Stukenborg, Jan-Bernd Blüher, Matthias Stumvoll, Michael Söder, Olle Svechnikov, Konstantin Fasshauer, Mathias Kralisch, Susan |
description | Obesity has recently been linked with reduced fertility, and the mechanisms underpinning this effect are currently unknown. The adipokine leptin is dysregulated in obesity and affects reproductive tracts; therefore, we investigated the dose-dependent effects of leptin on Leydig cell function and spermatogenesis. Eight-week-old leptin-deficient obese (ob/ob) male mice were treated with subphysiological (0.1- or 0.5-mg/kg body weight [BW]/d) or physiological (3.0-mg/kg BW/d) doses of leptin or saline for 12 weeks (chronic treatment) or 72 hours (acute treatment). We then evaluated male reproductive function markers. Mean testis weight increased significantly in the 0.1- and 3.0-mg/kg BW/d groups compared with saline controls (both P < .05). Intratesticular testosterone levels relative to testis weight significantly increased in the 0.5-mg/kg BW/d group compared with saline controls (P < .05). FSH levels increased in a dose-dependent manner with leptin treatment, whereas LH levels did not change. Leptin treatment significantly up-regulated both mRNA and protein expression of the steroidogenic enzyme cytochrome P450 17A1. Spermatogenesis improved in leptin-treated animals. Significantly more seminiferous tubules were observed in stages I–VIII (P < .01), and there were fewer abnormal seminiferous tubule structures (P < .01). Acute treatment with physiological leptin doses partially improved male reproductive markers without changing BW. Administration of subphysiological to physiological doses of leptin improves Leydig cell function and spermatogenesis. |
doi_str_mv | 10.1210/en.2015-1966 |
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The adipokine leptin is dysregulated in obesity and affects reproductive tracts; therefore, we investigated the dose-dependent effects of leptin on Leydig cell function and spermatogenesis. Eight-week-old leptin-deficient obese (ob/ob) male mice were treated with subphysiological (0.1- or 0.5-mg/kg body weight [BW]/d) or physiological (3.0-mg/kg BW/d) doses of leptin or saline for 12 weeks (chronic treatment) or 72 hours (acute treatment). We then evaluated male reproductive function markers. Mean testis weight increased significantly in the 0.1- and 3.0-mg/kg BW/d groups compared with saline controls (both P < .05). Intratesticular testosterone levels relative to testis weight significantly increased in the 0.5-mg/kg BW/d group compared with saline controls (P < .05). FSH levels increased in a dose-dependent manner with leptin treatment, whereas LH levels did not change. Leptin treatment significantly up-regulated both mRNA and protein expression of the steroidogenic enzyme cytochrome P450 17A1. Spermatogenesis improved in leptin-treated animals. Significantly more seminiferous tubules were observed in stages I–VIII (P < .01), and there were fewer abnormal seminiferous tubule structures (P < .01). Acute treatment with physiological leptin doses partially improved male reproductive markers without changing BW. Administration of subphysiological to physiological doses of leptin improves Leydig cell function and spermatogenesis.</description><identifier>ISSN: 0013-7227</identifier><identifier>ISSN: 1945-7170</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/en.2015-1966</identifier><identifier>PMID: 27105383</identifier><language>eng</language><publisher>United States: Endocrine Society</publisher><subject>Animals ; Body weight ; Cytochrome P450 ; Cytochromes P450 ; Enzyme-Linked Immunosorbent Assay ; Fertility ; Follicle Stimulating Hormone - metabolism ; Follicle-stimulating hormone ; Gene expression ; Leptin ; Leptin - pharmacology ; Leydig Cells - drug effects ; Male ; Males ; Medicin och hälsovetenskap ; Mice ; Mice, Obese ; mRNA ; Obesity ; Organ Size - drug effects ; Physiological effects ; Physiology ; Real-Time Polymerase Chain Reaction ; Seminiferous tubule ; Seminiferous Tubules - drug effects ; Spermatogenesis ; Spermatogenesis - drug effects ; Steroid 17-alpha-Hydroxylase - genetics ; Steroid 17-alpha-Hydroxylase - metabolism ; Testes ; Testis - drug effects ; Testosterone ; Testosterone - metabolism ; Tubules</subject><ispartof>Endocrinology (Philadelphia), 2016-06, Vol.157 (6), p.2461-2468</ispartof><rights>Copyright © 2016 by the Endocrine Society</rights><rights>Copyright © 2016 by the Endocrine Society 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c554t-f98e74a93d9fd368131b50a194828c9824d83a63e04a0a1401e82dd337e7d6f53</citedby><cites>FETCH-LOGICAL-c554t-f98e74a93d9fd368131b50a194828c9824d83a63e04a0a1401e82dd337e7d6f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27105383$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:133662012$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoffmann, Annett</creatorcontrib><creatorcontrib>Manjowk, Gloria-Maria</creatorcontrib><creatorcontrib>Wagner, Isabel Viola</creatorcontrib><creatorcontrib>Klöting, Nora</creatorcontrib><creatorcontrib>Ebert, Thomas</creatorcontrib><creatorcontrib>Jessnitzer, Beate</creatorcontrib><creatorcontrib>Lössner, Ulrike</creatorcontrib><creatorcontrib>Stukenborg, Jan-Bernd</creatorcontrib><creatorcontrib>Blüher, Matthias</creatorcontrib><creatorcontrib>Stumvoll, Michael</creatorcontrib><creatorcontrib>Söder, Olle</creatorcontrib><creatorcontrib>Svechnikov, Konstantin</creatorcontrib><creatorcontrib>Fasshauer, Mathias</creatorcontrib><creatorcontrib>Kralisch, Susan</creatorcontrib><title>Leptin Within the Subphysiological to Physiological Range Dose Dependently Improves Male Reproductive Function in an Obesity Mouse Model</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>Obesity has recently been linked with reduced fertility, and the mechanisms underpinning this effect are currently unknown. The adipokine leptin is dysregulated in obesity and affects reproductive tracts; therefore, we investigated the dose-dependent effects of leptin on Leydig cell function and spermatogenesis. Eight-week-old leptin-deficient obese (ob/ob) male mice were treated with subphysiological (0.1- or 0.5-mg/kg body weight [BW]/d) or physiological (3.0-mg/kg BW/d) doses of leptin or saline for 12 weeks (chronic treatment) or 72 hours (acute treatment). We then evaluated male reproductive function markers. Mean testis weight increased significantly in the 0.1- and 3.0-mg/kg BW/d groups compared with saline controls (both P < .05). Intratesticular testosterone levels relative to testis weight significantly increased in the 0.5-mg/kg BW/d group compared with saline controls (P < .05). FSH levels increased in a dose-dependent manner with leptin treatment, whereas LH levels did not change. Leptin treatment significantly up-regulated both mRNA and protein expression of the steroidogenic enzyme cytochrome P450 17A1. Spermatogenesis improved in leptin-treated animals. Significantly more seminiferous tubules were observed in stages I–VIII (P < .01), and there were fewer abnormal seminiferous tubule structures (P < .01). Acute treatment with physiological leptin doses partially improved male reproductive markers without changing BW. Administration of subphysiological to physiological doses of leptin improves Leydig cell function and spermatogenesis.</description><subject>Animals</subject><subject>Body weight</subject><subject>Cytochrome P450</subject><subject>Cytochromes P450</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Fertility</subject><subject>Follicle Stimulating Hormone - metabolism</subject><subject>Follicle-stimulating hormone</subject><subject>Gene expression</subject><subject>Leptin</subject><subject>Leptin - pharmacology</subject><subject>Leydig Cells - drug effects</subject><subject>Male</subject><subject>Males</subject><subject>Medicin och hälsovetenskap</subject><subject>Mice</subject><subject>Mice, Obese</subject><subject>mRNA</subject><subject>Obesity</subject><subject>Organ Size - drug effects</subject><subject>Physiological effects</subject><subject>Physiology</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Seminiferous tubule</subject><subject>Seminiferous Tubules - drug effects</subject><subject>Spermatogenesis</subject><subject>Spermatogenesis - drug effects</subject><subject>Steroid 17-alpha-Hydroxylase - genetics</subject><subject>Steroid 17-alpha-Hydroxylase - metabolism</subject><subject>Testes</subject><subject>Testis - drug effects</subject><subject>Testosterone</subject><subject>Testosterone - metabolism</subject><subject>Tubules</subject><issn>0013-7227</issn><issn>1945-7170</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFksFu1DAQhi0EokvhxhlZ4gAHUuzYiZ1jVShU2lVRAXG0nHjSdcnaIU6K9g14bGaVbSsQFRfbM_rm94z9E_KcsyOec_YWwlHOeJHxqiwfkAWvZJEprthDsmCMi0zluTogT1K6wlBKKR6Tg1xxVggtFuTXEvrRB_rNj2vcxjXQz1Pdr7fJxy5e-sZ2dIz00x-JCxsugb6LCRfoITgIY7elZ5t-iNeQ6Mp2QC8AIzc1o78GejoFPMRA8Q4b6HkNyY9buooTaqyig-4pedTaLsGz_X5Ivp6-_3LyMVuefzg7OV5mTVHIMWsrDUraSriqdaLUXPC6YBan1rluKp1Lp4UtBTBpMS0ZB507J4QC5cq2EIckm3XTT-in2vSD39hha6L1Zp_6jicwBStKXSJf3cvvBrwruinkQpQlfkmOta_nWgR_TJBGs_Gpga6zAXByw3XFtUZQ_h9VlagYk4Ih-vIv9CpOQ8BHM4ILpphUTCP1ZqaaIaY0QHvbOWdmZxwDweyMY3bGQfzFXnSqN-Bu4RunIPBqBuLU3yeV7aXETKIxYjP4gEaAlO66_GcDvwEEGdxQ</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Hoffmann, Annett</creator><creator>Manjowk, Gloria-Maria</creator><creator>Wagner, Isabel Viola</creator><creator>Klöting, Nora</creator><creator>Ebert, Thomas</creator><creator>Jessnitzer, Beate</creator><creator>Lössner, Ulrike</creator><creator>Stukenborg, Jan-Bernd</creator><creator>Blüher, Matthias</creator><creator>Stumvoll, Michael</creator><creator>Söder, Olle</creator><creator>Svechnikov, Konstantin</creator><creator>Fasshauer, Mathias</creator><creator>Kralisch, Susan</creator><general>Endocrine Society</general><general>Oxford University Press</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>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><scope>7X8</scope><scope>ADTPV</scope><scope>AOWAS</scope></search><sort><creationdate>20160601</creationdate><title>Leptin Within the Subphysiological to Physiological Range Dose Dependently Improves Male Reproductive Function in an Obesity Mouse Model</title><author>Hoffmann, Annett ; Manjowk, Gloria-Maria ; Wagner, Isabel Viola ; Klöting, Nora ; Ebert, Thomas ; Jessnitzer, Beate ; Lössner, Ulrike ; Stukenborg, Jan-Bernd ; Blüher, Matthias ; Stumvoll, Michael ; Söder, Olle ; Svechnikov, Konstantin ; Fasshauer, Mathias ; Kralisch, Susan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c554t-f98e74a93d9fd368131b50a194828c9824d83a63e04a0a1401e82dd337e7d6f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Body weight</topic><topic>Cytochrome P450</topic><topic>Cytochromes P450</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Fertility</topic><topic>Follicle Stimulating Hormone - metabolism</topic><topic>Follicle-stimulating hormone</topic><topic>Gene expression</topic><topic>Leptin</topic><topic>Leptin - pharmacology</topic><topic>Leydig Cells - drug effects</topic><topic>Male</topic><topic>Males</topic><topic>Medicin och hälsovetenskap</topic><topic>Mice</topic><topic>Mice, Obese</topic><topic>mRNA</topic><topic>Obesity</topic><topic>Organ Size - drug effects</topic><topic>Physiological effects</topic><topic>Physiology</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Seminiferous tubule</topic><topic>Seminiferous Tubules - drug effects</topic><topic>Spermatogenesis</topic><topic>Spermatogenesis - drug effects</topic><topic>Steroid 17-alpha-Hydroxylase - genetics</topic><topic>Steroid 17-alpha-Hydroxylase - metabolism</topic><topic>Testes</topic><topic>Testis - drug effects</topic><topic>Testosterone</topic><topic>Testosterone - metabolism</topic><topic>Tubules</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoffmann, Annett</creatorcontrib><creatorcontrib>Manjowk, Gloria-Maria</creatorcontrib><creatorcontrib>Wagner, Isabel Viola</creatorcontrib><creatorcontrib>Klöting, Nora</creatorcontrib><creatorcontrib>Ebert, Thomas</creatorcontrib><creatorcontrib>Jessnitzer, Beate</creatorcontrib><creatorcontrib>Lössner, Ulrike</creatorcontrib><creatorcontrib>Stukenborg, Jan-Bernd</creatorcontrib><creatorcontrib>Blüher, Matthias</creatorcontrib><creatorcontrib>Stumvoll, Michael</creatorcontrib><creatorcontrib>Söder, Olle</creatorcontrib><creatorcontrib>Svechnikov, Konstantin</creatorcontrib><creatorcontrib>Fasshauer, Mathias</creatorcontrib><creatorcontrib>Kralisch, Susan</creatorcontrib><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>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><collection>MEDLINE - Academic</collection><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoffmann, Annett</au><au>Manjowk, Gloria-Maria</au><au>Wagner, Isabel Viola</au><au>Klöting, Nora</au><au>Ebert, Thomas</au><au>Jessnitzer, Beate</au><au>Lössner, Ulrike</au><au>Stukenborg, Jan-Bernd</au><au>Blüher, Matthias</au><au>Stumvoll, Michael</au><au>Söder, Olle</au><au>Svechnikov, Konstantin</au><au>Fasshauer, Mathias</au><au>Kralisch, Susan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leptin Within the Subphysiological to Physiological Range Dose Dependently Improves Male Reproductive Function in an Obesity Mouse Model</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>2016-06-01</date><risdate>2016</risdate><volume>157</volume><issue>6</issue><spage>2461</spage><epage>2468</epage><pages>2461-2468</pages><issn>0013-7227</issn><issn>1945-7170</issn><eissn>1945-7170</eissn><abstract>Obesity has recently been linked with reduced fertility, and the mechanisms underpinning this effect are currently unknown. The adipokine leptin is dysregulated in obesity and affects reproductive tracts; therefore, we investigated the dose-dependent effects of leptin on Leydig cell function and spermatogenesis. Eight-week-old leptin-deficient obese (ob/ob) male mice were treated with subphysiological (0.1- or 0.5-mg/kg body weight [BW]/d) or physiological (3.0-mg/kg BW/d) doses of leptin or saline for 12 weeks (chronic treatment) or 72 hours (acute treatment). We then evaluated male reproductive function markers. Mean testis weight increased significantly in the 0.1- and 3.0-mg/kg BW/d groups compared with saline controls (both P < .05). Intratesticular testosterone levels relative to testis weight significantly increased in the 0.5-mg/kg BW/d group compared with saline controls (P < .05). FSH levels increased in a dose-dependent manner with leptin treatment, whereas LH levels did not change. Leptin treatment significantly up-regulated both mRNA and protein expression of the steroidogenic enzyme cytochrome P450 17A1. Spermatogenesis improved in leptin-treated animals. Significantly more seminiferous tubules were observed in stages I–VIII (P < .01), and there were fewer abnormal seminiferous tubule structures (P < .01). Acute treatment with physiological leptin doses partially improved male reproductive markers without changing BW. Administration of subphysiological to physiological doses of leptin improves Leydig cell function and spermatogenesis.</abstract><cop>United States</cop><pub>Endocrine Society</pub><pmid>27105383</pmid><doi>10.1210/en.2015-1966</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Body weight Cytochrome P450 Cytochromes P450 Enzyme-Linked Immunosorbent Assay Fertility Follicle Stimulating Hormone - metabolism Follicle-stimulating hormone Gene expression Leptin Leptin - pharmacology Leydig Cells - drug effects Male Males Medicin och hälsovetenskap Mice Mice, Obese mRNA Obesity Organ Size - drug effects Physiological effects Physiology Real-Time Polymerase Chain Reaction Seminiferous tubule Seminiferous Tubules - drug effects Spermatogenesis Spermatogenesis - drug effects Steroid 17-alpha-Hydroxylase - genetics Steroid 17-alpha-Hydroxylase - metabolism Testes Testis - drug effects Testosterone Testosterone - metabolism Tubules |
title | Leptin Within the Subphysiological to Physiological Range Dose Dependently Improves Male Reproductive Function in an Obesity Mouse Model |
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