Periosteal Remodeling at the Femoral Neck in Nonhuman Primates

Periosteal bone turnover is poorly understood. We documented intramembranous periosteal bone turnover in the femoral neck in intact nonhuman primates and an increase in osteoclast numbers at the periosteal surface in sex steroid–deficient animals. Our studies are the first to systematically document...

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Veröffentlicht in:Journal of bone and mineral research 2006-07, Vol.21 (7), p.1060-1067
Hauptverfasser: Bliziotes, Michael, Sibonga, Jean D, Turner, Russell T, Orwoll, Eric
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container_end_page 1067
container_issue 7
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container_title Journal of bone and mineral research
container_volume 21
creator Bliziotes, Michael
Sibonga, Jean D
Turner, Russell T
Orwoll, Eric
description Periosteal bone turnover is poorly understood. We documented intramembranous periosteal bone turnover in the femoral neck in intact nonhuman primates and an increase in osteoclast numbers at the periosteal surface in sex steroid–deficient animals. Our studies are the first to systematically document periosteal turnover at the femoral neck. Introduction: Bone size is an important determinant of bone strength, and cellular events at the periosteal surface could alter bone dimensions. We characterized periosteal cellular activity with dynamic histomorphometric studies of nonhuman primate femoral neck and shaft. Materials and Methods: Femur specimens from 16 intact adult male and female nonhuman primates (Rhesus [Macaca mulatta, n = 9] and Japanese Macaque [Macaca fuscata, n = 7]) were analyzed. Animals were double‐labeled with tetracycline, and necropsy was performed 2–7 days after the last dose. We characterized periosteal resorptive activity in an additional group of five intact and four castrate female animals. Multiple group comparisons in intact animals were performed by one‐way ANOVA followed by a Fisher PLSD posthoc test. In gonadectomized animals, Fisher's exact test was used for dichotomous and Mann‐Whitney U‐test for continuous variables. Results: Bone turnover in the periosteum of the femoral neck in intact animals was more rapid than at the femoral shaft but slower than in femoral neck cancellous bone. Similarly, in these intact animals, the eroded surface of cortical bone at the femoral neck periosteal surface was significantly greater than in the cancellous bone compartment (p < 0.0001) or on the femoral shaft (p < 0.0001). Gonadectomized female animals showed an increase in osteoclast number on the periosteal surface compared with intact controls (p < 0.01). Conclusions: We documented intramembranous periosteal bone turnover in the femoral neck by histomorphometric analyses. The tissue level bone formation rate was sufficient to add substantively to femoral neck size over time. Periosteal osteoclastic activity was not the result of the emergence of intracortical tunneling at the bone surface. Sex steroid deficiency produced an increase in osteoclast numbers at the periosteal surface. This is the first systematic documentation of periosteal turnover at the femoral neck.
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We documented intramembranous periosteal bone turnover in the femoral neck in intact nonhuman primates and an increase in osteoclast numbers at the periosteal surface in sex steroid–deficient animals. Our studies are the first to systematically document periosteal turnover at the femoral neck. Introduction: Bone size is an important determinant of bone strength, and cellular events at the periosteal surface could alter bone dimensions. We characterized periosteal cellular activity with dynamic histomorphometric studies of nonhuman primate femoral neck and shaft. Materials and Methods: Femur specimens from 16 intact adult male and female nonhuman primates (Rhesus [Macaca mulatta, n = 9] and Japanese Macaque [Macaca fuscata, n = 7]) were analyzed. Animals were double‐labeled with tetracycline, and necropsy was performed 2–7 days after the last dose. We characterized periosteal resorptive activity in an additional group of five intact and four castrate female animals. Multiple group comparisons in intact animals were performed by one‐way ANOVA followed by a Fisher PLSD posthoc test. In gonadectomized animals, Fisher's exact test was used for dichotomous and Mann‐Whitney U‐test for continuous variables. Results: Bone turnover in the periosteum of the femoral neck in intact animals was more rapid than at the femoral shaft but slower than in femoral neck cancellous bone. Similarly, in these intact animals, the eroded surface of cortical bone at the femoral neck periosteal surface was significantly greater than in the cancellous bone compartment (p &lt; 0.0001) or on the femoral shaft (p &lt; 0.0001). Gonadectomized female animals showed an increase in osteoclast number on the periosteal surface compared with intact controls (p &lt; 0.01). Conclusions: We documented intramembranous periosteal bone turnover in the femoral neck by histomorphometric analyses. The tissue level bone formation rate was sufficient to add substantively to femoral neck size over time. Periosteal osteoclastic activity was not the result of the emergence of intracortical tunneling at the bone surface. Sex steroid deficiency produced an increase in osteoclast numbers at the periosteal surface. 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Psychology ; Macaca fuscata ; Macaca mulatta ; Male ; modeling and remodeling ; Orchiectomy ; osteoblasts ; Osteoclasts - cytology ; Osteoclasts - physiology ; Ovariectomy ; periosteum ; Periosteum - cytology ; Periosteum - physiology ; primate ; Primates ; Skeleton and joints ; Vertebrates: osteoarticular system, musculoskeletal system</subject><ispartof>Journal of bone and mineral research, 2006-07, Vol.21 (7), p.1060-1067</ispartof><rights>Copyright © 2006 ASBMR</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4339-e2b56bcb9e114b6c79fda5b5a5833fee4690207f426051fa9175c4e72349d1ba3</citedby><cites>FETCH-LOGICAL-c4339-e2b56bcb9e114b6c79fda5b5a5833fee4690207f426051fa9175c4e72349d1ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1359%2Fjbmr.060414$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1359%2Fjbmr.060414$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17948025$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16813526$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bliziotes, Michael</creatorcontrib><creatorcontrib>Sibonga, Jean D</creatorcontrib><creatorcontrib>Turner, Russell T</creatorcontrib><creatorcontrib>Orwoll, Eric</creatorcontrib><title>Periosteal Remodeling at the Femoral Neck in Nonhuman Primates</title><title>Journal of bone and mineral research</title><addtitle>J Bone Miner Res</addtitle><description>Periosteal bone turnover is poorly understood. We documented intramembranous periosteal bone turnover in the femoral neck in intact nonhuman primates and an increase in osteoclast numbers at the periosteal surface in sex steroid–deficient animals. Our studies are the first to systematically document periosteal turnover at the femoral neck. Introduction: Bone size is an important determinant of bone strength, and cellular events at the periosteal surface could alter bone dimensions. We characterized periosteal cellular activity with dynamic histomorphometric studies of nonhuman primate femoral neck and shaft. Materials and Methods: Femur specimens from 16 intact adult male and female nonhuman primates (Rhesus [Macaca mulatta, n = 9] and Japanese Macaque [Macaca fuscata, n = 7]) were analyzed. Animals were double‐labeled with tetracycline, and necropsy was performed 2–7 days after the last dose. We characterized periosteal resorptive activity in an additional group of five intact and four castrate female animals. Multiple group comparisons in intact animals were performed by one‐way ANOVA followed by a Fisher PLSD posthoc test. In gonadectomized animals, Fisher's exact test was used for dichotomous and Mann‐Whitney U‐test for continuous variables. Results: Bone turnover in the periosteum of the femoral neck in intact animals was more rapid than at the femoral shaft but slower than in femoral neck cancellous bone. Similarly, in these intact animals, the eroded surface of cortical bone at the femoral neck periosteal surface was significantly greater than in the cancellous bone compartment (p &lt; 0.0001) or on the femoral shaft (p &lt; 0.0001). Gonadectomized female animals showed an increase in osteoclast number on the periosteal surface compared with intact controls (p &lt; 0.01). Conclusions: We documented intramembranous periosteal bone turnover in the femoral neck by histomorphometric analyses. The tissue level bone formation rate was sufficient to add substantively to femoral neck size over time. Periosteal osteoclastic activity was not the result of the emergence of intracortical tunneling at the bone surface. Sex steroid deficiency produced an increase in osteoclast numbers at the periosteal surface. This is the first systematic documentation of periosteal turnover at the femoral neck.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>bone histomorphometry</subject><subject>bone mineralization</subject><subject>Bone Resorption - metabolism</subject><subject>Female</subject><subject>Femur Neck - cytology</subject><subject>Femur Neck - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Macaca fuscata</subject><subject>Macaca mulatta</subject><subject>Male</subject><subject>modeling and remodeling</subject><subject>Orchiectomy</subject><subject>osteoblasts</subject><subject>Osteoclasts - cytology</subject><subject>Osteoclasts - physiology</subject><subject>Ovariectomy</subject><subject>periosteum</subject><subject>Periosteum - cytology</subject><subject>Periosteum - physiology</subject><subject>primate</subject><subject>Primates</subject><subject>Skeleton and joints</subject><subject>Vertebrates: osteoarticular system, musculoskeletal system</subject><issn>0884-0431</issn><issn>1523-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0EtLw0AQB_BFFFurJ--Si14kdTb7SPYiaLE-qLUUPYfNdmJT86i7CdJvb0ILvelpYObHDPMn5JzCkDKhblZJYYcggVN-QPpUBMznMqKHpA9RxH3gjPbIiXMrAJBCymPSo-2ciUD2ye0MbVa5GnXuzbGoFphn5aena69eojduO7adTNF8eVnpTaty2RS69GY2K3SN7pQcpTp3eLarA_IxfngfPfmTt8fn0d3EN5wx5WOQCJmYRCGlPJEmVOlCi0RoETGWInKpIIAw5YEEQVOtaCgMxzBgXC1ootmAXG33rm313aCr4yJzBvNcl1g1LpaRBKCR-BdSxRWTrIPXW2hs5ZzFNF53P9lNTCHuco27XONtrq2-2K1tkgIXe7sLsgWXO6Cd0XlqdWkyt3eh4hEE3dlw636yHDd_3Yxf7l_nQgoIKISg2C_8aI-b</recordid><startdate>200607</startdate><enddate>200607</enddate><creator>Bliziotes, Michael</creator><creator>Sibonga, Jean D</creator><creator>Turner, Russell T</creator><creator>Orwoll, Eric</creator><general>John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR)</general><general>American Society for Bone and Mineral Research</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>200607</creationdate><title>Periosteal Remodeling at the Femoral Neck in Nonhuman Primates</title><author>Bliziotes, Michael ; Sibonga, Jean D ; Turner, Russell T ; Orwoll, Eric</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4339-e2b56bcb9e114b6c79fda5b5a5833fee4690207f426051fa9175c4e72349d1ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>bone histomorphometry</topic><topic>bone mineralization</topic><topic>Bone Resorption - metabolism</topic><topic>Female</topic><topic>Femur Neck - cytology</topic><topic>Femur Neck - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Macaca fuscata</topic><topic>Macaca mulatta</topic><topic>Male</topic><topic>modeling and remodeling</topic><topic>Orchiectomy</topic><topic>osteoblasts</topic><topic>Osteoclasts - cytology</topic><topic>Osteoclasts - physiology</topic><topic>Ovariectomy</topic><topic>periosteum</topic><topic>Periosteum - cytology</topic><topic>Periosteum - physiology</topic><topic>primate</topic><topic>Primates</topic><topic>Skeleton and joints</topic><topic>Vertebrates: osteoarticular system, musculoskeletal system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bliziotes, Michael</creatorcontrib><creatorcontrib>Sibonga, Jean D</creatorcontrib><creatorcontrib>Turner, Russell T</creatorcontrib><creatorcontrib>Orwoll, Eric</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of bone and mineral research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bliziotes, Michael</au><au>Sibonga, Jean D</au><au>Turner, Russell T</au><au>Orwoll, Eric</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Periosteal Remodeling at the Femoral Neck in Nonhuman Primates</atitle><jtitle>Journal of bone and mineral research</jtitle><addtitle>J Bone Miner Res</addtitle><date>2006-07</date><risdate>2006</risdate><volume>21</volume><issue>7</issue><spage>1060</spage><epage>1067</epage><pages>1060-1067</pages><issn>0884-0431</issn><eissn>1523-4681</eissn><coden>JBMREJ</coden><abstract>Periosteal bone turnover is poorly understood. We documented intramembranous periosteal bone turnover in the femoral neck in intact nonhuman primates and an increase in osteoclast numbers at the periosteal surface in sex steroid–deficient animals. Our studies are the first to systematically document periosteal turnover at the femoral neck. Introduction: Bone size is an important determinant of bone strength, and cellular events at the periosteal surface could alter bone dimensions. We characterized periosteal cellular activity with dynamic histomorphometric studies of nonhuman primate femoral neck and shaft. Materials and Methods: Femur specimens from 16 intact adult male and female nonhuman primates (Rhesus [Macaca mulatta, n = 9] and Japanese Macaque [Macaca fuscata, n = 7]) were analyzed. Animals were double‐labeled with tetracycline, and necropsy was performed 2–7 days after the last dose. We characterized periosteal resorptive activity in an additional group of five intact and four castrate female animals. Multiple group comparisons in intact animals were performed by one‐way ANOVA followed by a Fisher PLSD posthoc test. In gonadectomized animals, Fisher's exact test was used for dichotomous and Mann‐Whitney U‐test for continuous variables. Results: Bone turnover in the periosteum of the femoral neck in intact animals was more rapid than at the femoral shaft but slower than in femoral neck cancellous bone. Similarly, in these intact animals, the eroded surface of cortical bone at the femoral neck periosteal surface was significantly greater than in the cancellous bone compartment (p &lt; 0.0001) or on the femoral shaft (p &lt; 0.0001). Gonadectomized female animals showed an increase in osteoclast number on the periosteal surface compared with intact controls (p &lt; 0.01). Conclusions: We documented intramembranous periosteal bone turnover in the femoral neck by histomorphometric analyses. The tissue level bone formation rate was sufficient to add substantively to femoral neck size over time. Periosteal osteoclastic activity was not the result of the emergence of intracortical tunneling at the bone surface. Sex steroid deficiency produced an increase in osteoclast numbers at the periosteal surface. This is the first systematic documentation of periosteal turnover at the femoral neck.</abstract><cop>Washington, DC</cop><pub>John Wiley and Sons and The American Society for Bone and Mineral Research (ASBMR)</pub><pmid>16813526</pmid><doi>10.1359/jbmr.060414</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current)
subjects Animals
Biological and medical sciences
bone histomorphometry
bone mineralization
Bone Resorption - metabolism
Female
Femur Neck - cytology
Femur Neck - physiology
Fundamental and applied biological sciences. Psychology
Macaca fuscata
Macaca mulatta
Male
modeling and remodeling
Orchiectomy
osteoblasts
Osteoclasts - cytology
Osteoclasts - physiology
Ovariectomy
periosteum
Periosteum - cytology
Periosteum - physiology
primate
Primates
Skeleton and joints
Vertebrates: osteoarticular system, musculoskeletal system
title Periosteal Remodeling at the Femoral Neck in Nonhuman Primates
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