Loss of sex-specific difference in femoral bone parameters in male leptin knockout mice
Sex-dependent differences were identified in the femoral bone parameters of male and female ob/ob (leptin knockout) mice compared with their C57BL/6 wild-type background strain. Total fat, lean weight and body weight were not different between adult male and female leptin knockout mice. However, lep...
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description | Sex-dependent differences were identified in the femoral bone parameters of male and female ob/ob (leptin knockout) mice compared with their C57BL/6 wild-type background strain. Total fat, lean weight and body weight were not different between adult male and female leptin knockout mice. However, leptin knockout males exhibited lower lean weights than C57BL/6 males. Peripheral quantitative computerized tomographic measurements at the femoral midshaft revealed that the normal differences in the periosteal circumference, endosteal circumference, total bone mineral content, and polar moment of inertia normally observed between adult male and female wild-type mice were lost between adult male and female ob/ob mice. Significant reductions in these bone parameters were seen in male ob/ob mice compared to male wild-type mice but not in female ob/ob mice compared to female wild-type mice. In prepubertal mice, there were no differences in phenotype and femoral bone parameters between males and females within any strain, suggesting sex hormone functions. Serum free testosterone levels were 5.6-fold higher in adult male ob/ob mice than in adult male C57BL/6 wild-type mice, and serum estradiol levels were 1.8- and 1.3-fold greater in adult male and female ob/ob mice, respectively, than in their wild-type counterparts. Androgen receptor gene expression was not different in femur-derived bone cells of male ob/ob mice compared with wild-type mice. The loss of sex-related differences in these bone parameters in adult male ob/ob mice might result from deficient signaling in the androgen signaling pathway and the fact that leptin functions are permissive for androgen effects on bone development. |
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Total fat, lean weight and body weight were not different between adult male and female leptin knockout mice. However, leptin knockout males exhibited lower lean weights than C57BL/6 males. Peripheral quantitative computerized tomographic measurements at the femoral midshaft revealed that the normal differences in the periosteal circumference, endosteal circumference, total bone mineral content, and polar moment of inertia normally observed between adult male and female wild-type mice were lost between adult male and female ob/ob mice. Significant reductions in these bone parameters were seen in male ob/ob mice compared to male wild-type mice but not in female ob/ob mice compared to female wild-type mice. In prepubertal mice, there were no differences in phenotype and femoral bone parameters between males and females within any strain, suggesting sex hormone functions. Serum free testosterone levels were 5.6-fold higher in adult male ob/ob mice than in adult male C57BL/6 wild-type mice, and serum estradiol levels were 1.8- and 1.3-fold greater in adult male and female ob/ob mice, respectively, than in their wild-type counterparts. Androgen receptor gene expression was not different in femur-derived bone cells of male ob/ob mice compared with wild-type mice. The loss of sex-related differences in these bone parameters in adult male ob/ob mice might result from deficient signaling in the androgen signaling pathway and the fact that leptin functions are permissive for androgen effects on bone development.</description><identifier>ISSN: 0171-967X</identifier><identifier>EISSN: 1432-0827</identifier><identifier>DOI: 10.1007/s00223-007-9026-0</identifier><identifier>PMID: 17516018</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Androgens - metabolism ; Animals ; Body Weight ; Bone and Bones - metabolism ; Bone Density ; Bones ; Comparative studies ; Female ; Femur - metabolism ; Femur - pathology ; Gender differences ; Genetics ; Genotype & phenotype ; Leptin - genetics ; Leptin - metabolism ; Leptin - physiology ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Receptors, Androgen - metabolism ; Rodents ; Sex Factors ; Tomography ; Tomography, X-Ray Computed - methods</subject><ispartof>Calcified tissue international, 2007-06, Vol.80 (6), p.374-382</ispartof><rights>Springer Science+Business Media, LLC 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-ab1254a8fecfd96d46c0a271415c11d5207905495e41151b29752d4faf8a2b893</citedby><cites>FETCH-LOGICAL-c357t-ab1254a8fecfd96d46c0a271415c11d5207905495e41151b29752d4faf8a2b893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17516018$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Xiaoguang</creatorcontrib><creatorcontrib>Rundle, Charles H</creatorcontrib><creatorcontrib>Wergedal, Jon E</creatorcontrib><creatorcontrib>Srivastava, Apurva K</creatorcontrib><creatorcontrib>Mohan, Subburaman</creatorcontrib><creatorcontrib>Lau, K-H William</creatorcontrib><title>Loss of sex-specific difference in femoral bone parameters in male leptin knockout mice</title><title>Calcified tissue international</title><addtitle>Calcif Tissue Int</addtitle><description>Sex-dependent differences were identified in the femoral bone parameters of male and female ob/ob (leptin knockout) mice compared with their C57BL/6 wild-type background strain. Total fat, lean weight and body weight were not different between adult male and female leptin knockout mice. However, leptin knockout males exhibited lower lean weights than C57BL/6 males. Peripheral quantitative computerized tomographic measurements at the femoral midshaft revealed that the normal differences in the periosteal circumference, endosteal circumference, total bone mineral content, and polar moment of inertia normally observed between adult male and female wild-type mice were lost between adult male and female ob/ob mice. Significant reductions in these bone parameters were seen in male ob/ob mice compared to male wild-type mice but not in female ob/ob mice compared to female wild-type mice. In prepubertal mice, there were no differences in phenotype and femoral bone parameters between males and females within any strain, suggesting sex hormone functions. Serum free testosterone levels were 5.6-fold higher in adult male ob/ob mice than in adult male C57BL/6 wild-type mice, and serum estradiol levels were 1.8- and 1.3-fold greater in adult male and female ob/ob mice, respectively, than in their wild-type counterparts. Androgen receptor gene expression was not different in femur-derived bone cells of male ob/ob mice compared with wild-type mice. The loss of sex-related differences in these bone parameters in adult male ob/ob mice might result from deficient signaling in the androgen signaling pathway and the fact that leptin functions are permissive for androgen effects on bone development.</description><subject>Androgens - metabolism</subject><subject>Animals</subject><subject>Body Weight</subject><subject>Bone and Bones - metabolism</subject><subject>Bone Density</subject><subject>Bones</subject><subject>Comparative studies</subject><subject>Female</subject><subject>Femur - metabolism</subject><subject>Femur - pathology</subject><subject>Gender differences</subject><subject>Genetics</subject><subject>Genotype & phenotype</subject><subject>Leptin - genetics</subject><subject>Leptin - metabolism</subject><subject>Leptin - physiology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Receptors, Androgen - metabolism</subject><subject>Rodents</subject><subject>Sex Factors</subject><subject>Tomography</subject><subject>Tomography, X-Ray Computed - methods</subject><issn>0171-967X</issn><issn>1432-0827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkU9r1UAUxQdR7Gv1A7iR4MLd6L2T-ZNZSqlWeODGUnfDZHIH0iaZOJOA_fZNeA8EN67ugfs7B-49jL1D-IQA5nMBEKLmm-QWhObwgh1Q1oJDI8xLdgA0yK02vy7YZSkPACi11q_ZBRqFGrA5sPtjKqVKsSr0h5eZQh_7UHV9jJRpClT1UxVpTNkPVZsmqmaf_UgL5bKvRj9QNdC8bPpxSuExrUs19oHesFfRD4XenucVu_t68_P6lh9_fPt-_eXIQ63Mwn2LQknfRAqxs7qTOoAXBiWqgNgpAcaCklaRRFTYCmuU6GT0sfGibWx9xT6ecuecfq9UFjf2JdAw-InSWpwBLWQt5X9BAdJqrZoN_PAP-JDWPG1HOIHCqlrBDuEJCnn7X6bo5tyPPj85BLd3407duF3u3TjYPO_PwWs7UvfXcS6jfgYMl4h1</recordid><startdate>20070601</startdate><enddate>20070601</enddate><creator>Wang, Xiaoguang</creator><creator>Rundle, Charles H</creator><creator>Wergedal, Jon E</creator><creator>Srivastava, Apurva K</creator><creator>Mohan, Subburaman</creator><creator>Lau, K-H William</creator><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20070601</creationdate><title>Loss of sex-specific difference in femoral bone parameters in male leptin knockout mice</title><author>Wang, Xiaoguang ; Rundle, Charles H ; Wergedal, Jon E ; Srivastava, Apurva K ; Mohan, Subburaman ; Lau, K-H William</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-ab1254a8fecfd96d46c0a271415c11d5207905495e41151b29752d4faf8a2b893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Androgens - metabolism</topic><topic>Animals</topic><topic>Body Weight</topic><topic>Bone and Bones - metabolism</topic><topic>Bone Density</topic><topic>Bones</topic><topic>Comparative studies</topic><topic>Female</topic><topic>Femur - metabolism</topic><topic>Femur - pathology</topic><topic>Gender differences</topic><topic>Genetics</topic><topic>Genotype & phenotype</topic><topic>Leptin - genetics</topic><topic>Leptin - metabolism</topic><topic>Leptin - physiology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Receptors, Androgen - metabolism</topic><topic>Rodents</topic><topic>Sex Factors</topic><topic>Tomography</topic><topic>Tomography, X-Ray Computed - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Xiaoguang</creatorcontrib><creatorcontrib>Rundle, Charles H</creatorcontrib><creatorcontrib>Wergedal, Jon E</creatorcontrib><creatorcontrib>Srivastava, Apurva K</creatorcontrib><creatorcontrib>Mohan, Subburaman</creatorcontrib><creatorcontrib>Lau, K-H William</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Calcified tissue international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Xiaoguang</au><au>Rundle, Charles H</au><au>Wergedal, Jon E</au><au>Srivastava, Apurva K</au><au>Mohan, Subburaman</au><au>Lau, K-H William</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Loss of sex-specific difference in femoral bone parameters in male leptin knockout mice</atitle><jtitle>Calcified tissue international</jtitle><addtitle>Calcif Tissue Int</addtitle><date>2007-06-01</date><risdate>2007</risdate><volume>80</volume><issue>6</issue><spage>374</spage><epage>382</epage><pages>374-382</pages><issn>0171-967X</issn><eissn>1432-0827</eissn><abstract>Sex-dependent differences were identified in the femoral bone parameters of male and female ob/ob (leptin knockout) mice compared with their C57BL/6 wild-type background strain. Total fat, lean weight and body weight were not different between adult male and female leptin knockout mice. However, leptin knockout males exhibited lower lean weights than C57BL/6 males. Peripheral quantitative computerized tomographic measurements at the femoral midshaft revealed that the normal differences in the periosteal circumference, endosteal circumference, total bone mineral content, and polar moment of inertia normally observed between adult male and female wild-type mice were lost between adult male and female ob/ob mice. Significant reductions in these bone parameters were seen in male ob/ob mice compared to male wild-type mice but not in female ob/ob mice compared to female wild-type mice. In prepubertal mice, there were no differences in phenotype and femoral bone parameters between males and females within any strain, suggesting sex hormone functions. Serum free testosterone levels were 5.6-fold higher in adult male ob/ob mice than in adult male C57BL/6 wild-type mice, and serum estradiol levels were 1.8- and 1.3-fold greater in adult male and female ob/ob mice, respectively, than in their wild-type counterparts. Androgen receptor gene expression was not different in femur-derived bone cells of male ob/ob mice compared with wild-type mice. The loss of sex-related differences in these bone parameters in adult male ob/ob mice might result from deficient signaling in the androgen signaling pathway and the fact that leptin functions are permissive for androgen effects on bone development.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>17516018</pmid><doi>10.1007/s00223-007-9026-0</doi><tpages>9</tpages></addata></record> |
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subjects | Androgens - metabolism Animals Body Weight Bone and Bones - metabolism Bone Density Bones Comparative studies Female Femur - metabolism Femur - pathology Gender differences Genetics Genotype & phenotype Leptin - genetics Leptin - metabolism Leptin - physiology Male Mice Mice, Inbred C57BL Mice, Knockout Receptors, Androgen - metabolism Rodents Sex Factors Tomography Tomography, X-Ray Computed - methods |
title | Loss of sex-specific difference in femoral bone parameters in male leptin knockout mice |
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