Understanding How Sex Influences the Impact of IL-10 on Bone Microarchitecture and Bone Metabolism Over Time

Dietary interventions with pre- and probiotics favorably affect the gut-bone axis, mediated in part by the anti-inflammatory cytokine, interleukin (IL)-10. This study sought to understand how IL-10’s impact on bone metabolism and microarchitecture differs with sex and time. Six-week-old B6.129P2-Il1...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Current developments in nutrition 2021-06, Vol.5 (Supplement_2), p.1138-1138
Hauptverfasser: Price, Payton, Perez, Leo, Hatter, Bethany, Robinson, Kara, Islam, Proapa, Alake, Sanmi, Ice, John, Lucas, Edralin, Smith, Brenda
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1138
container_issue Supplement_2
container_start_page 1138
container_title Current developments in nutrition
container_volume 5
creator Price, Payton
Perez, Leo
Hatter, Bethany
Robinson, Kara
Islam, Proapa
Alake, Sanmi
Ice, John
Lucas, Edralin
Smith, Brenda
description Dietary interventions with pre- and probiotics favorably affect the gut-bone axis, mediated in part by the anti-inflammatory cytokine, interleukin (IL)-10. This study sought to understand how IL-10’s impact on bone metabolism and microarchitecture differs with sex and time. Six-week-old B6.129P2-Il10tm1Cgn/J (KO) and C57BL/6 (WT) mice were assigned in a 2 × 2 × 2 factorial design with strain (WT & KO), sex, and time (3 & 6 m) as factors. Mice were fed AIN-93G diet for 3 m followed by AIN-93 M for the study duration. Dual-energy x-ray absorptiometry was used to assess bone mineral content (BMC) and density (BMD). Micro-computed tomography was used to assess femur and lumbar vertebrae trabecular and cortical bone. Serum procollagen 1 intact N-terminal propeptide (P1NP) and C-terminal telopeptide of type I collagen (CTX-1), bone formation and resorption markers respectively, were assessed by ELISA. Data were analyzed using ANOVA; p < 0.05 was considered significant. Reductions in BMC and BMD (P < 0.05) in KO vs WT and at 3 vs 6 m were observed; a sex effect was found with reductions in BMC in KO females compared to KO males. Femoral trabecular bone volume (BV/TV) was lower (P < 0.05) in KO vs WT, females vs males, and at 6 vs 3 m. Trabecular thickness (TbTh) decreased (P < 0.05) in KO vs WT and increased from 3 to 6 m, while decreases in trabecular number (TbN) were greater (P < 0.05) in KO mice, females, and at 6 m compared to counterparts. Cortical area and thickness were decreased (P < 0.05) in KO vs WT and in females vs males, which was greater at 6 m, while cortical bone porosity was higher in KO vs WT and increased at 6 mo. Vertebral trabecular BV/TV was lower (P < 0.05) in KO vs WT at 3 and 6 m, with KO females showing reduced BV/TV (P < 0.05) from 3 to 6 m. Reduced TbTh and TbN were observed in KO vs WT, and females had increased (P < 0.05) TbTh and trabecular separation and reduced TbN. P1NP showed a time effect (P < 0.05) with reductions in WT females and males at 6 m compared to 3 m KO females (P < 0.05). CTX-1 shows a sex effect (P < 0.05) and a trending strain effect (P = 0.059), with elevated serum CTX-1 in 3 m KO males compared to WT and KO females at 6 m (P < 0.05). While IL-10 plays an important role in maintaining both trabecular and cortical bone, it may have a more protective effect on the cortical bone of female mice over time. Oklahoma Agricultural Experiment Station.
doi_str_mv 10.1093/cdn/nzab061_022
format Article
fullrecord <record><control><sourceid>oup_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1093_cdn_nzab061_022</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/cdn/nzab061_022</oup_id><els_id>S2475299123116568</els_id><sourcerecordid>10.1093/cdn/nzab061_022</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1662-740fb36efebd5ea3d2c7b54cc2b9555577a55ff569a0ac43109db822043830cd3</originalsourceid><addsrcrecordid>eNqNkM1PAjEQxRujiQQ5e-3ZZKXtftGjEpVNMByEc9Ntp1LDtqRd8OOvtwQOXEycy0wy773M_BC6peSeEp6PlXZj9yNbUlFBGLtAA1bUZcY4p5dn8zUaxfhBCKGc84rwAdqsnIYQe-m0de945j_xG3zhxpnNDpyCiPs14KbbStVjb3AzzyjB3uFH7wC_WhW8DGpte1D9LgBOOacV9LL1Gxs7vNhDwEvbwQ26MnITYXTqQ7R6flpOZ9l88dJMH-aZolXFsrogps0rMNDqEmSumarbslCKtbxMVdeyLI0pKy6JVEWeCOh2whgp8klOlM6HaHzMTdfFGMCIbbCdDN-CEnHgJRIvccYrOe6ODr_b_kPMj2JIP-wtBBGVPcDSNiQMQnv7p_cXTPSBdw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Understanding How Sex Influences the Impact of IL-10 on Bone Microarchitecture and Bone Metabolism Over Time</title><source>Oxford Journals Open Access Collection</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><creator>Price, Payton ; Perez, Leo ; Hatter, Bethany ; Robinson, Kara ; Islam, Proapa ; Alake, Sanmi ; Ice, John ; Lucas, Edralin ; Smith, Brenda</creator><creatorcontrib>Price, Payton ; Perez, Leo ; Hatter, Bethany ; Robinson, Kara ; Islam, Proapa ; Alake, Sanmi ; Ice, John ; Lucas, Edralin ; Smith, Brenda</creatorcontrib><description><![CDATA[Dietary interventions with pre- and probiotics favorably affect the gut-bone axis, mediated in part by the anti-inflammatory cytokine, interleukin (IL)-10. This study sought to understand how IL-10’s impact on bone metabolism and microarchitecture differs with sex and time. Six-week-old B6.129P2-Il10tm1Cgn/J (KO) and C57BL/6 (WT) mice were assigned in a 2 × 2 × 2 factorial design with strain (WT & KO), sex, and time (3 & 6 m) as factors. Mice were fed AIN-93G diet for 3 m followed by AIN-93 M for the study duration. Dual-energy x-ray absorptiometry was used to assess bone mineral content (BMC) and density (BMD). Micro-computed tomography was used to assess femur and lumbar vertebrae trabecular and cortical bone. Serum procollagen 1 intact N-terminal propeptide (P1NP) and C-terminal telopeptide of type I collagen (CTX-1), bone formation and resorption markers respectively, were assessed by ELISA. Data were analyzed using ANOVA; p < 0.05 was considered significant. Reductions in BMC and BMD (P < 0.05) in KO vs WT and at 3 vs 6 m were observed; a sex effect was found with reductions in BMC in KO females compared to KO males. Femoral trabecular bone volume (BV/TV) was lower (P < 0.05) in KO vs WT, females vs males, and at 6 vs 3 m. Trabecular thickness (TbTh) decreased (P < 0.05) in KO vs WT and increased from 3 to 6 m, while decreases in trabecular number (TbN) were greater (P < 0.05) in KO mice, females, and at 6 m compared to counterparts. Cortical area and thickness were decreased (P < 0.05) in KO vs WT and in females vs males, which was greater at 6 m, while cortical bone porosity was higher in KO vs WT and increased at 6 mo. Vertebral trabecular BV/TV was lower (P < 0.05) in KO vs WT at 3 and 6 m, with KO females showing reduced BV/TV (P < 0.05) from 3 to 6 m. Reduced TbTh and TbN were observed in KO vs WT, and females had increased (P < 0.05) TbTh and trabecular separation and reduced TbN. P1NP showed a time effect (P < 0.05) with reductions in WT females and males at 6 m compared to 3 m KO females (P < 0.05). CTX-1 shows a sex effect (P < 0.05) and a trending strain effect (P = 0.059), with elevated serum CTX-1 in 3 m KO males compared to WT and KO females at 6 m (P < 0.05). While IL-10 plays an important role in maintaining both trabecular and cortical bone, it may have a more protective effect on the cortical bone of female mice over time. Oklahoma Agricultural Experiment Station.]]></description><identifier>ISSN: 2475-2991</identifier><identifier>EISSN: 2475-2991</identifier><identifier>DOI: 10.1093/cdn/nzab061_022</identifier><language>eng</language><publisher>Elsevier Inc</publisher><ispartof>Current developments in nutrition, 2021-06, Vol.5 (Supplement_2), p.1138-1138</ispartof><rights>2021 American Society for Nutrition.</rights><rights>Copyright © The Author(s) on behalf of the American Society for Nutrition 2021. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Price, Payton</creatorcontrib><creatorcontrib>Perez, Leo</creatorcontrib><creatorcontrib>Hatter, Bethany</creatorcontrib><creatorcontrib>Robinson, Kara</creatorcontrib><creatorcontrib>Islam, Proapa</creatorcontrib><creatorcontrib>Alake, Sanmi</creatorcontrib><creatorcontrib>Ice, John</creatorcontrib><creatorcontrib>Lucas, Edralin</creatorcontrib><creatorcontrib>Smith, Brenda</creatorcontrib><title>Understanding How Sex Influences the Impact of IL-10 on Bone Microarchitecture and Bone Metabolism Over Time</title><title>Current developments in nutrition</title><description><![CDATA[Dietary interventions with pre- and probiotics favorably affect the gut-bone axis, mediated in part by the anti-inflammatory cytokine, interleukin (IL)-10. This study sought to understand how IL-10’s impact on bone metabolism and microarchitecture differs with sex and time. Six-week-old B6.129P2-Il10tm1Cgn/J (KO) and C57BL/6 (WT) mice were assigned in a 2 × 2 × 2 factorial design with strain (WT & KO), sex, and time (3 & 6 m) as factors. Mice were fed AIN-93G diet for 3 m followed by AIN-93 M for the study duration. Dual-energy x-ray absorptiometry was used to assess bone mineral content (BMC) and density (BMD). Micro-computed tomography was used to assess femur and lumbar vertebrae trabecular and cortical bone. Serum procollagen 1 intact N-terminal propeptide (P1NP) and C-terminal telopeptide of type I collagen (CTX-1), bone formation and resorption markers respectively, were assessed by ELISA. Data were analyzed using ANOVA; p < 0.05 was considered significant. Reductions in BMC and BMD (P < 0.05) in KO vs WT and at 3 vs 6 m were observed; a sex effect was found with reductions in BMC in KO females compared to KO males. Femoral trabecular bone volume (BV/TV) was lower (P < 0.05) in KO vs WT, females vs males, and at 6 vs 3 m. Trabecular thickness (TbTh) decreased (P < 0.05) in KO vs WT and increased from 3 to 6 m, while decreases in trabecular number (TbN) were greater (P < 0.05) in KO mice, females, and at 6 m compared to counterparts. Cortical area and thickness were decreased (P < 0.05) in KO vs WT and in females vs males, which was greater at 6 m, while cortical bone porosity was higher in KO vs WT and increased at 6 mo. Vertebral trabecular BV/TV was lower (P < 0.05) in KO vs WT at 3 and 6 m, with KO females showing reduced BV/TV (P < 0.05) from 3 to 6 m. Reduced TbTh and TbN were observed in KO vs WT, and females had increased (P < 0.05) TbTh and trabecular separation and reduced TbN. P1NP showed a time effect (P < 0.05) with reductions in WT females and males at 6 m compared to 3 m KO females (P < 0.05). CTX-1 shows a sex effect (P < 0.05) and a trending strain effect (P = 0.059), with elevated serum CTX-1 in 3 m KO males compared to WT and KO females at 6 m (P < 0.05). While IL-10 plays an important role in maintaining both trabecular and cortical bone, it may have a more protective effect on the cortical bone of female mice over time. Oklahoma Agricultural Experiment Station.]]></description><issn>2475-2991</issn><issn>2475-2991</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqNkM1PAjEQxRujiQQ5e-3ZZKXtftGjEpVNMByEc9Ntp1LDtqRd8OOvtwQOXEycy0wy773M_BC6peSeEp6PlXZj9yNbUlFBGLtAA1bUZcY4p5dn8zUaxfhBCKGc84rwAdqsnIYQe-m0de945j_xG3zhxpnNDpyCiPs14KbbStVjb3AzzyjB3uFH7wC_WhW8DGpte1D9LgBOOacV9LL1Gxs7vNhDwEvbwQ26MnITYXTqQ7R6flpOZ9l88dJMH-aZolXFsrogps0rMNDqEmSumarbslCKtbxMVdeyLI0pKy6JVEWeCOh2whgp8klOlM6HaHzMTdfFGMCIbbCdDN-CEnHgJRIvccYrOe6ODr_b_kPMj2JIP-wtBBGVPcDSNiQMQnv7p_cXTPSBdw</recordid><startdate>202106</startdate><enddate>202106</enddate><creator>Price, Payton</creator><creator>Perez, Leo</creator><creator>Hatter, Bethany</creator><creator>Robinson, Kara</creator><creator>Islam, Proapa</creator><creator>Alake, Sanmi</creator><creator>Ice, John</creator><creator>Lucas, Edralin</creator><creator>Smith, Brenda</creator><general>Elsevier Inc</general><general>Oxford University Press</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>202106</creationdate><title>Understanding How Sex Influences the Impact of IL-10 on Bone Microarchitecture and Bone Metabolism Over Time</title><author>Price, Payton ; Perez, Leo ; Hatter, Bethany ; Robinson, Kara ; Islam, Proapa ; Alake, Sanmi ; Ice, John ; Lucas, Edralin ; Smith, Brenda</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1662-740fb36efebd5ea3d2c7b54cc2b9555577a55ff569a0ac43109db822043830cd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Price, Payton</creatorcontrib><creatorcontrib>Perez, Leo</creatorcontrib><creatorcontrib>Hatter, Bethany</creatorcontrib><creatorcontrib>Robinson, Kara</creatorcontrib><creatorcontrib>Islam, Proapa</creatorcontrib><creatorcontrib>Alake, Sanmi</creatorcontrib><creatorcontrib>Ice, John</creatorcontrib><creatorcontrib>Lucas, Edralin</creatorcontrib><creatorcontrib>Smith, Brenda</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><jtitle>Current developments in nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Price, Payton</au><au>Perez, Leo</au><au>Hatter, Bethany</au><au>Robinson, Kara</au><au>Islam, Proapa</au><au>Alake, Sanmi</au><au>Ice, John</au><au>Lucas, Edralin</au><au>Smith, Brenda</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Understanding How Sex Influences the Impact of IL-10 on Bone Microarchitecture and Bone Metabolism Over Time</atitle><jtitle>Current developments in nutrition</jtitle><date>2021-06</date><risdate>2021</risdate><volume>5</volume><issue>Supplement_2</issue><spage>1138</spage><epage>1138</epage><pages>1138-1138</pages><issn>2475-2991</issn><eissn>2475-2991</eissn><abstract><![CDATA[Dietary interventions with pre- and probiotics favorably affect the gut-bone axis, mediated in part by the anti-inflammatory cytokine, interleukin (IL)-10. This study sought to understand how IL-10’s impact on bone metabolism and microarchitecture differs with sex and time. Six-week-old B6.129P2-Il10tm1Cgn/J (KO) and C57BL/6 (WT) mice were assigned in a 2 × 2 × 2 factorial design with strain (WT & KO), sex, and time (3 & 6 m) as factors. Mice were fed AIN-93G diet for 3 m followed by AIN-93 M for the study duration. Dual-energy x-ray absorptiometry was used to assess bone mineral content (BMC) and density (BMD). Micro-computed tomography was used to assess femur and lumbar vertebrae trabecular and cortical bone. Serum procollagen 1 intact N-terminal propeptide (P1NP) and C-terminal telopeptide of type I collagen (CTX-1), bone formation and resorption markers respectively, were assessed by ELISA. Data were analyzed using ANOVA; p < 0.05 was considered significant. Reductions in BMC and BMD (P < 0.05) in KO vs WT and at 3 vs 6 m were observed; a sex effect was found with reductions in BMC in KO females compared to KO males. Femoral trabecular bone volume (BV/TV) was lower (P < 0.05) in KO vs WT, females vs males, and at 6 vs 3 m. Trabecular thickness (TbTh) decreased (P < 0.05) in KO vs WT and increased from 3 to 6 m, while decreases in trabecular number (TbN) were greater (P < 0.05) in KO mice, females, and at 6 m compared to counterparts. Cortical area and thickness were decreased (P < 0.05) in KO vs WT and in females vs males, which was greater at 6 m, while cortical bone porosity was higher in KO vs WT and increased at 6 mo. Vertebral trabecular BV/TV was lower (P < 0.05) in KO vs WT at 3 and 6 m, with KO females showing reduced BV/TV (P < 0.05) from 3 to 6 m. Reduced TbTh and TbN were observed in KO vs WT, and females had increased (P < 0.05) TbTh and trabecular separation and reduced TbN. P1NP showed a time effect (P < 0.05) with reductions in WT females and males at 6 m compared to 3 m KO females (P < 0.05). CTX-1 shows a sex effect (P < 0.05) and a trending strain effect (P = 0.059), with elevated serum CTX-1 in 3 m KO males compared to WT and KO females at 6 m (P < 0.05). While IL-10 plays an important role in maintaining both trabecular and cortical bone, it may have a more protective effect on the cortical bone of female mice over time. Oklahoma Agricultural Experiment Station.]]></abstract><pub>Elsevier Inc</pub><doi>10.1093/cdn/nzab061_022</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2475-2991
ispartof Current developments in nutrition, 2021-06, Vol.5 (Supplement_2), p.1138-1138
issn 2475-2991
2475-2991
language eng
recordid cdi_crossref_primary_10_1093_cdn_nzab061_022
source Oxford Journals Open Access Collection; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
title Understanding How Sex Influences the Impact of IL-10 on Bone Microarchitecture and Bone Metabolism Over Time
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-14T00%3A32%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-oup_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Understanding%20How%20Sex%20Influences%20the%20Impact%20of%20IL-10%20on%20Bone%20Microarchitecture%20and%20Bone%20Metabolism%20Over%20Time&rft.jtitle=Current%20developments%20in%20nutrition&rft.au=Price,%20Payton&rft.date=2021-06&rft.volume=5&rft.issue=Supplement_2&rft.spage=1138&rft.epage=1138&rft.pages=1138-1138&rft.issn=2475-2991&rft.eissn=2475-2991&rft_id=info:doi/10.1093/cdn/nzab061_022&rft_dat=%3Coup_cross%3E10.1093/cdn/nzab061_022%3C/oup_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_oup_id=10.1093/cdn/nzab061_022&rft_els_id=S2475299123116568&rfr_iscdi=true