Purslane Suppresses Osteoclast Differentiation and Bone Resorbing Activity via Inhibition of Akt/GSK3β-c-Fos-NFATc1 Signaling in Vitro and Prevents Lipopolysaccharide-Induced Bone Loss in Vivo

Purslane (Portulaca oleracea L.) is popular as a potherb in many areas of Europe, Asia, and the Mediterranean region and is widely distributed around the globe. It has a wide range of pharmacological effects, such as antibacterial, anti-aging, anti-inflammatory, and anti-oxidative properties. Althou...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biological & pharmaceutical bulletin 2015/01/01, Vol.38(1), pp.66-74
Hauptverfasser: Kim, Ju-Young, Oh, Hyun Mee, Kwak, Sung Chul, Cheon, Yoon-Hee, Lee, Myeung Su, Rho, Mun Chual, Oh, Jaemin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 74
container_issue 1
container_start_page 66
container_title Biological & pharmaceutical bulletin
container_volume 38
creator Kim, Ju-Young
Oh, Hyun Mee
Kwak, Sung Chul
Cheon, Yoon-Hee
Lee, Myeung Su
Rho, Mun Chual
Oh, Jaemin
description Purslane (Portulaca oleracea L.) is popular as a potherb in many areas of Europe, Asia, and the Mediterranean region and is widely distributed around the globe. It has a wide range of pharmacological effects, such as antibacterial, anti-aging, anti-inflammatory, and anti-oxidative properties. Although the extract of purslane has numerous beneficial pharmacological effects, its effect on osteoclasts remains unknown. We aimed to investigate the anti-osteoclastogenic activity in vitro and in vivo and to elucidate the underlying mechanism. The effect of purslane on the differentiation and function of bone marrow-derived macrophages (BMMs) into osteoclasts was examined using a phenotype assay such as tartrate-resistant acid phosphatase (TRAP) staining, F-actin staining, and pit assay and followed by confirmation by real-time reverse transcription polymerase chain reaction (RT-PCR) and Western blot analysis. To address the effect of purslane in vivo, the inflammatory, lipopolysaccharide (LPS)-induced osteolysis mouse model was chosen. Bone volume and bone microarchitecture were evaluated by microcomputed tomography and histologic analysis. Purslane inhibited receptor activator of nuclear factor-kappa B ligand (RANKL)-stimulated osteoclast differentiation accompanied by inhibition of Akt/glycogen synthase kinase 3β (GSK3β) signaling, which could underlie purslane-induced downregulation of c-Fos and nuclear factor of activated T cells 1 (NFATc1) expression levels, transcription factors that regulate osteoclast-specific genes, as well as osteoclast fusion and resorption-related molecules. Moreover, in vivo studies further verified the bone protection activity of purslane in the LPS-induced osteolysis animal model. Purslane could exhibit its anti-osteoclastogenic activity by inhibiting Akt/GSK3β-c-Fos-NFATc1 signaling cascades. Therefore, purslane is a potential natural medicine for the treatment of osteoclast-related diseases.
doi_str_mv 10.1248/bpb.b14-00567
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1837328537</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1661330840</sourcerecordid><originalsourceid>FETCH-LOGICAL-c515t-616eaa10113f705895f6dd28fc05f1b6ec0baeef8f101a486154ed42f0215ce43</originalsourceid><addsrcrecordid>eNqFkcFy0zAQhj0MDA2FI1dGRy5qJUuy1WMIpGTItB1SuHpkeZWqOJYryZnJa_EGvADPhJyEXHvZPey3_87-f5a9p-SC5lxe1n19UVOOCRFF-SKbUMZLLHIqXmYTckUlLqiQZ9mbEB4JISXJ2evsLBcl57wgk-zP3eBDqzpAq6HvPYQAAd2GCE63KkT02RoDHrpoVbSuQ6pr0CeX8O8QnK9tt0ZTHe3Wxh3aWoUW3YOt7R51Bk1_xcvr1Tf29zfWeO4CvplP7zVFK7vuVDsu2w79tNG7vfCdh206FdDS9q537S4orR-Utw3gRdcMGo7Hly6Ew-rWvc1eGdUGeHfs59mP-Zf72Ve8vL1ezKZLrAUVMdlQgFKUUMpMSYS8EqZomlwaTYShdQGa1ArASJMYxWWyjUPDc0OSlxo4O88-HnR7754GCLHa2KChHc1zQ6ioZCXLpUj1WbQoKGNEcpJQfEC1Tz95MFXv7Ub5XUVJNQZcpYCrFHC1DzjxH47SQ72B5kT_TzQBswPwGKJawwlQPlrdwl6OyYqO5SR7mo5uV9Cxf9iivJY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1661330840</pqid></control><display><type>article</type><title>Purslane Suppresses Osteoclast Differentiation and Bone Resorbing Activity via Inhibition of Akt/GSK3β-c-Fos-NFATc1 Signaling in Vitro and Prevents Lipopolysaccharide-Induced Bone Loss in Vivo</title><source>J-STAGE Free</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Free Full-Text Journals in Chemistry</source><creator>Kim, Ju-Young ; Oh, Hyun Mee ; Kwak, Sung Chul ; Cheon, Yoon-Hee ; Lee, Myeung Su ; Rho, Mun Chual ; Oh, Jaemin</creator><creatorcontrib>Kim, Ju-Young ; Oh, Hyun Mee ; Kwak, Sung Chul ; Cheon, Yoon-Hee ; Lee, Myeung Su ; Rho, Mun Chual ; Oh, Jaemin</creatorcontrib><description>Purslane (Portulaca oleracea L.) is popular as a potherb in many areas of Europe, Asia, and the Mediterranean region and is widely distributed around the globe. It has a wide range of pharmacological effects, such as antibacterial, anti-aging, anti-inflammatory, and anti-oxidative properties. Although the extract of purslane has numerous beneficial pharmacological effects, its effect on osteoclasts remains unknown. We aimed to investigate the anti-osteoclastogenic activity in vitro and in vivo and to elucidate the underlying mechanism. The effect of purslane on the differentiation and function of bone marrow-derived macrophages (BMMs) into osteoclasts was examined using a phenotype assay such as tartrate-resistant acid phosphatase (TRAP) staining, F-actin staining, and pit assay and followed by confirmation by real-time reverse transcription polymerase chain reaction (RT-PCR) and Western blot analysis. To address the effect of purslane in vivo, the inflammatory, lipopolysaccharide (LPS)-induced osteolysis mouse model was chosen. Bone volume and bone microarchitecture were evaluated by microcomputed tomography and histologic analysis. Purslane inhibited receptor activator of nuclear factor-kappa B ligand (RANKL)-stimulated osteoclast differentiation accompanied by inhibition of Akt/glycogen synthase kinase 3β (GSK3β) signaling, which could underlie purslane-induced downregulation of c-Fos and nuclear factor of activated T cells 1 (NFATc1) expression levels, transcription factors that regulate osteoclast-specific genes, as well as osteoclast fusion and resorption-related molecules. Moreover, in vivo studies further verified the bone protection activity of purslane in the LPS-induced osteolysis animal model. Purslane could exhibit its anti-osteoclastogenic activity by inhibiting Akt/GSK3β-c-Fos-NFATc1 signaling cascades. Therefore, purslane is a potential natural medicine for the treatment of osteoclast-related diseases.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.b14-00567</identifier><identifier>PMID: 25744460</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Animals ; bone loss ; Bone Marrow Cells - cytology ; Bone Resorption - chemically induced ; Bone Resorption - metabolism ; Bone Resorption - prevention &amp; control ; Cell Differentiation - drug effects ; Glycogen Synthase Kinase 3 - antagonists &amp; inhibitors ; Glycogen Synthase Kinase 3 - metabolism ; Glycogen Synthase Kinase 3 beta ; Lipopolysaccharides ; Male ; Mice, Inbred ICR ; natural medicine ; NFATC Transcription Factors - antagonists &amp; inhibitors ; NFATC Transcription Factors - metabolism ; osteoclast ; Osteoclasts - cytology ; Osteoclasts - drug effects ; Osteoclasts - metabolism ; osteoporosis ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; Portulaca ; Portulaca oleracea ; Proto-Oncogene Proteins c-akt - antagonists &amp; inhibitors ; Proto-Oncogene Proteins c-akt - metabolism ; Proto-Oncogene Proteins c-fos - antagonists &amp; inhibitors ; Proto-Oncogene Proteins c-fos - metabolism ; purslane (Portulaca oleracea) ; RANK Ligand - pharmacology ; Signal Transduction - drug effects</subject><ispartof>Biological and Pharmaceutical Bulletin, 2015/01/01, Vol.38(1), pp.66-74</ispartof><rights>2015 The Pharmaceutical Society of Japan</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c515t-616eaa10113f705895f6dd28fc05f1b6ec0baeef8f101a486154ed42f0215ce43</citedby><cites>FETCH-LOGICAL-c515t-616eaa10113f705895f6dd28fc05f1b6ec0baeef8f101a486154ed42f0215ce43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25744460$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Ju-Young</creatorcontrib><creatorcontrib>Oh, Hyun Mee</creatorcontrib><creatorcontrib>Kwak, Sung Chul</creatorcontrib><creatorcontrib>Cheon, Yoon-Hee</creatorcontrib><creatorcontrib>Lee, Myeung Su</creatorcontrib><creatorcontrib>Rho, Mun Chual</creatorcontrib><creatorcontrib>Oh, Jaemin</creatorcontrib><title>Purslane Suppresses Osteoclast Differentiation and Bone Resorbing Activity via Inhibition of Akt/GSK3β-c-Fos-NFATc1 Signaling in Vitro and Prevents Lipopolysaccharide-Induced Bone Loss in Vivo</title><title>Biological &amp; pharmaceutical bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>Purslane (Portulaca oleracea L.) is popular as a potherb in many areas of Europe, Asia, and the Mediterranean region and is widely distributed around the globe. It has a wide range of pharmacological effects, such as antibacterial, anti-aging, anti-inflammatory, and anti-oxidative properties. Although the extract of purslane has numerous beneficial pharmacological effects, its effect on osteoclasts remains unknown. We aimed to investigate the anti-osteoclastogenic activity in vitro and in vivo and to elucidate the underlying mechanism. The effect of purslane on the differentiation and function of bone marrow-derived macrophages (BMMs) into osteoclasts was examined using a phenotype assay such as tartrate-resistant acid phosphatase (TRAP) staining, F-actin staining, and pit assay and followed by confirmation by real-time reverse transcription polymerase chain reaction (RT-PCR) and Western blot analysis. To address the effect of purslane in vivo, the inflammatory, lipopolysaccharide (LPS)-induced osteolysis mouse model was chosen. Bone volume and bone microarchitecture were evaluated by microcomputed tomography and histologic analysis. Purslane inhibited receptor activator of nuclear factor-kappa B ligand (RANKL)-stimulated osteoclast differentiation accompanied by inhibition of Akt/glycogen synthase kinase 3β (GSK3β) signaling, which could underlie purslane-induced downregulation of c-Fos and nuclear factor of activated T cells 1 (NFATc1) expression levels, transcription factors that regulate osteoclast-specific genes, as well as osteoclast fusion and resorption-related molecules. Moreover, in vivo studies further verified the bone protection activity of purslane in the LPS-induced osteolysis animal model. Purslane could exhibit its anti-osteoclastogenic activity by inhibiting Akt/GSK3β-c-Fos-NFATc1 signaling cascades. Therefore, purslane is a potential natural medicine for the treatment of osteoclast-related diseases.</description><subject>Animals</subject><subject>bone loss</subject><subject>Bone Marrow Cells - cytology</subject><subject>Bone Resorption - chemically induced</subject><subject>Bone Resorption - metabolism</subject><subject>Bone Resorption - prevention &amp; control</subject><subject>Cell Differentiation - drug effects</subject><subject>Glycogen Synthase Kinase 3 - antagonists &amp; inhibitors</subject><subject>Glycogen Synthase Kinase 3 - metabolism</subject><subject>Glycogen Synthase Kinase 3 beta</subject><subject>Lipopolysaccharides</subject><subject>Male</subject><subject>Mice, Inbred ICR</subject><subject>natural medicine</subject><subject>NFATC Transcription Factors - antagonists &amp; inhibitors</subject><subject>NFATC Transcription Factors - metabolism</subject><subject>osteoclast</subject><subject>Osteoclasts - cytology</subject><subject>Osteoclasts - drug effects</subject><subject>Osteoclasts - metabolism</subject><subject>osteoporosis</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>Portulaca</subject><subject>Portulaca oleracea</subject><subject>Proto-Oncogene Proteins c-akt - antagonists &amp; inhibitors</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Proto-Oncogene Proteins c-fos - antagonists &amp; inhibitors</subject><subject>Proto-Oncogene Proteins c-fos - metabolism</subject><subject>purslane (Portulaca oleracea)</subject><subject>RANK Ligand - pharmacology</subject><subject>Signal Transduction - drug effects</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFy0zAQhj0MDA2FI1dGRy5qJUuy1WMIpGTItB1SuHpkeZWqOJYryZnJa_EGvADPhJyEXHvZPey3_87-f5a9p-SC5lxe1n19UVOOCRFF-SKbUMZLLHIqXmYTckUlLqiQZ9mbEB4JISXJ2evsLBcl57wgk-zP3eBDqzpAq6HvPYQAAd2GCE63KkT02RoDHrpoVbSuQ6pr0CeX8O8QnK9tt0ZTHe3Wxh3aWoUW3YOt7R51Bk1_xcvr1Tf29zfWeO4CvplP7zVFK7vuVDsu2w79tNG7vfCdh206FdDS9q537S4orR-Utw3gRdcMGo7Hly6Ew-rWvc1eGdUGeHfs59mP-Zf72Ve8vL1ezKZLrAUVMdlQgFKUUMpMSYS8EqZomlwaTYShdQGa1ArASJMYxWWyjUPDc0OSlxo4O88-HnR7754GCLHa2KChHc1zQ6ioZCXLpUj1WbQoKGNEcpJQfEC1Tz95MFXv7Ub5XUVJNQZcpYCrFHC1DzjxH47SQ72B5kT_TzQBswPwGKJawwlQPlrdwl6OyYqO5SR7mo5uV9Cxf9iivJY</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Kim, Ju-Young</creator><creator>Oh, Hyun Mee</creator><creator>Kwak, Sung Chul</creator><creator>Cheon, Yoon-Hee</creator><creator>Lee, Myeung Su</creator><creator>Rho, Mun Chual</creator><creator>Oh, Jaemin</creator><general>The Pharmaceutical Society of Japan</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>7X8</scope><scope>7QP</scope></search><sort><creationdate>20150101</creationdate><title>Purslane Suppresses Osteoclast Differentiation and Bone Resorbing Activity via Inhibition of Akt/GSK3β-c-Fos-NFATc1 Signaling in Vitro and Prevents Lipopolysaccharide-Induced Bone Loss in Vivo</title><author>Kim, Ju-Young ; Oh, Hyun Mee ; Kwak, Sung Chul ; Cheon, Yoon-Hee ; Lee, Myeung Su ; Rho, Mun Chual ; Oh, Jaemin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-616eaa10113f705895f6dd28fc05f1b6ec0baeef8f101a486154ed42f0215ce43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>bone loss</topic><topic>Bone Marrow Cells - cytology</topic><topic>Bone Resorption - chemically induced</topic><topic>Bone Resorption - metabolism</topic><topic>Bone Resorption - prevention &amp; control</topic><topic>Cell Differentiation - drug effects</topic><topic>Glycogen Synthase Kinase 3 - antagonists &amp; inhibitors</topic><topic>Glycogen Synthase Kinase 3 - metabolism</topic><topic>Glycogen Synthase Kinase 3 beta</topic><topic>Lipopolysaccharides</topic><topic>Male</topic><topic>Mice, Inbred ICR</topic><topic>natural medicine</topic><topic>NFATC Transcription Factors - antagonists &amp; inhibitors</topic><topic>NFATC Transcription Factors - metabolism</topic><topic>osteoclast</topic><topic>Osteoclasts - cytology</topic><topic>Osteoclasts - drug effects</topic><topic>Osteoclasts - metabolism</topic><topic>osteoporosis</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Extracts - therapeutic use</topic><topic>Portulaca</topic><topic>Portulaca oleracea</topic><topic>Proto-Oncogene Proteins c-akt - antagonists &amp; inhibitors</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Proto-Oncogene Proteins c-fos - antagonists &amp; inhibitors</topic><topic>Proto-Oncogene Proteins c-fos - metabolism</topic><topic>purslane (Portulaca oleracea)</topic><topic>RANK Ligand - pharmacology</topic><topic>Signal Transduction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Ju-Young</creatorcontrib><creatorcontrib>Oh, Hyun Mee</creatorcontrib><creatorcontrib>Kwak, Sung Chul</creatorcontrib><creatorcontrib>Cheon, Yoon-Hee</creatorcontrib><creatorcontrib>Lee, Myeung Su</creatorcontrib><creatorcontrib>Rho, Mun Chual</creatorcontrib><creatorcontrib>Oh, Jaemin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><jtitle>Biological &amp; pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Ju-Young</au><au>Oh, Hyun Mee</au><au>Kwak, Sung Chul</au><au>Cheon, Yoon-Hee</au><au>Lee, Myeung Su</au><au>Rho, Mun Chual</au><au>Oh, Jaemin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Purslane Suppresses Osteoclast Differentiation and Bone Resorbing Activity via Inhibition of Akt/GSK3β-c-Fos-NFATc1 Signaling in Vitro and Prevents Lipopolysaccharide-Induced Bone Loss in Vivo</atitle><jtitle>Biological &amp; pharmaceutical bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>38</volume><issue>1</issue><spage>66</spage><epage>74</epage><pages>66-74</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>Purslane (Portulaca oleracea L.) is popular as a potherb in many areas of Europe, Asia, and the Mediterranean region and is widely distributed around the globe. It has a wide range of pharmacological effects, such as antibacterial, anti-aging, anti-inflammatory, and anti-oxidative properties. Although the extract of purslane has numerous beneficial pharmacological effects, its effect on osteoclasts remains unknown. We aimed to investigate the anti-osteoclastogenic activity in vitro and in vivo and to elucidate the underlying mechanism. The effect of purslane on the differentiation and function of bone marrow-derived macrophages (BMMs) into osteoclasts was examined using a phenotype assay such as tartrate-resistant acid phosphatase (TRAP) staining, F-actin staining, and pit assay and followed by confirmation by real-time reverse transcription polymerase chain reaction (RT-PCR) and Western blot analysis. To address the effect of purslane in vivo, the inflammatory, lipopolysaccharide (LPS)-induced osteolysis mouse model was chosen. Bone volume and bone microarchitecture were evaluated by microcomputed tomography and histologic analysis. Purslane inhibited receptor activator of nuclear factor-kappa B ligand (RANKL)-stimulated osteoclast differentiation accompanied by inhibition of Akt/glycogen synthase kinase 3β (GSK3β) signaling, which could underlie purslane-induced downregulation of c-Fos and nuclear factor of activated T cells 1 (NFATc1) expression levels, transcription factors that regulate osteoclast-specific genes, as well as osteoclast fusion and resorption-related molecules. Moreover, in vivo studies further verified the bone protection activity of purslane in the LPS-induced osteolysis animal model. Purslane could exhibit its anti-osteoclastogenic activity by inhibiting Akt/GSK3β-c-Fos-NFATc1 signaling cascades. Therefore, purslane is a potential natural medicine for the treatment of osteoclast-related diseases.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>25744460</pmid><doi>10.1248/bpb.b14-00567</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0918-6158
ispartof Biological and Pharmaceutical Bulletin, 2015/01/01, Vol.38(1), pp.66-74
issn 0918-6158
1347-5215
language eng
recordid cdi_proquest_miscellaneous_1837328537
source J-STAGE Free; MEDLINE; EZB-FREE-00999 freely available EZB journals; Free Full-Text Journals in Chemistry
subjects Animals
bone loss
Bone Marrow Cells - cytology
Bone Resorption - chemically induced
Bone Resorption - metabolism
Bone Resorption - prevention & control
Cell Differentiation - drug effects
Glycogen Synthase Kinase 3 - antagonists & inhibitors
Glycogen Synthase Kinase 3 - metabolism
Glycogen Synthase Kinase 3 beta
Lipopolysaccharides
Male
Mice, Inbred ICR
natural medicine
NFATC Transcription Factors - antagonists & inhibitors
NFATC Transcription Factors - metabolism
osteoclast
Osteoclasts - cytology
Osteoclasts - drug effects
Osteoclasts - metabolism
osteoporosis
Plant Extracts - pharmacology
Plant Extracts - therapeutic use
Portulaca
Portulaca oleracea
Proto-Oncogene Proteins c-akt - antagonists & inhibitors
Proto-Oncogene Proteins c-akt - metabolism
Proto-Oncogene Proteins c-fos - antagonists & inhibitors
Proto-Oncogene Proteins c-fos - metabolism
purslane (Portulaca oleracea)
RANK Ligand - pharmacology
Signal Transduction - drug effects
title Purslane Suppresses Osteoclast Differentiation and Bone Resorbing Activity via Inhibition of Akt/GSK3β-c-Fos-NFATc1 Signaling in Vitro and Prevents Lipopolysaccharide-Induced Bone Loss in Vivo
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T14%3A31%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Purslane%20Suppresses%20Osteoclast%20Differentiation%20and%20Bone%20Resorbing%20Activity%20via%20Inhibition%20of%20Akt/GSK3%CE%B2-c-Fos-NFATc1%20Signaling%20in%20Vitro%20and%20Prevents%20Lipopolysaccharide-Induced%20Bone%20Loss%20in%20Vivo&rft.jtitle=Biological%20&%20pharmaceutical%20bulletin&rft.au=Kim,%20Ju-Young&rft.date=2015-01-01&rft.volume=38&rft.issue=1&rft.spage=66&rft.epage=74&rft.pages=66-74&rft.issn=0918-6158&rft.eissn=1347-5215&rft_id=info:doi/10.1248/bpb.b14-00567&rft_dat=%3Cproquest_cross%3E1661330840%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1661330840&rft_id=info:pmid/25744460&rfr_iscdi=true