Combined Effects of Hydrogen Sulfide and Lipopolysaccharide on Osteoclast Differentiation in Rats

Background: Lipopolysaccharide (LPS) stimulates osteoclast differentiation through toll‐like receptors (TLRs) 2 and 4, and hydrogen sulfide (H2S) induces osteoclast differentiation. If H2S activates TLRs, H2S may enhance the effects of LPS on osteoclast differentiation. The purpose of the present st...

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Veröffentlicht in:Journal of periodontology (1970) 2012-04, Vol.83 (4), p.522-527
Hauptverfasser: Irie, Koichiro, Ekuni, Daisuke, Tomofuji, Takaaki, Endo, Yasumasa, Kasuyama, Kenta, Yaegaki, Ken, Morita, Manabu
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container_end_page 527
container_issue 4
container_start_page 522
container_title Journal of periodontology (1970)
container_volume 83
creator Irie, Koichiro
Ekuni, Daisuke
Tomofuji, Takaaki
Endo, Yasumasa
Kasuyama, Kenta
Yaegaki, Ken
Morita, Manabu
description Background: Lipopolysaccharide (LPS) stimulates osteoclast differentiation through toll‐like receptors (TLRs) 2 and 4, and hydrogen sulfide (H2S) induces osteoclast differentiation. If H2S activates TLRs, H2S may enhance the effects of LPS on osteoclast differentiation. The purpose of the present study is to examine the combined effects of sodium hydrogen sulfide (NaHS, an H2S donor drug) and LPS on osteoclast differentiation and TLR expression in rat periodontal tissue. Methods: Twenty‐eight male Wistar rats (8 weeks old) were divided into four groups (n = 7 per group): a control (no treatment) group and three experimental groups (NaHS group, LPS group, and a combination [NaHS + LPS] group). At 1 day after topical application of NaHS and/or Porphyromonas gingivalis LPS into the gingival sulcus of first molars, the number of tartrate‐resistant acid phosphate (TRAP)‐positive osteoclasts in the periodontal tissue was counted. Expression of TLR2 and TLR4 mRNAs and proteins in the gingival was also assessed. Results: The number of TRAP‐positive osteoclasts was significantly higher in the combination group than in any other group (P
doi_str_mv 10.1902/jop.2011.110315
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If H2S activates TLRs, H2S may enhance the effects of LPS on osteoclast differentiation. The purpose of the present study is to examine the combined effects of sodium hydrogen sulfide (NaHS, an H2S donor drug) and LPS on osteoclast differentiation and TLR expression in rat periodontal tissue. Methods: Twenty‐eight male Wistar rats (8 weeks old) were divided into four groups (n = 7 per group): a control (no treatment) group and three experimental groups (NaHS group, LPS group, and a combination [NaHS + LPS] group). At 1 day after topical application of NaHS and/or Porphyromonas gingivalis LPS into the gingival sulcus of first molars, the number of tartrate‐resistant acid phosphate (TRAP)‐positive osteoclasts in the periodontal tissue was counted. Expression of TLR2 and TLR4 mRNAs and proteins in the gingival was also assessed. Results: The number of TRAP‐positive osteoclasts was significantly higher in the combination group than in any other group (P &lt;0.01). The combination group had 11.0‐fold higher TLR4 mRNA levels than the control group. TLR4 protein levels were also higher in the combination group than in the NaHS or LPS group. However, the TLR2 mRNA and protein levels were not significantly different in the combination group and the LPS group. Conclusion: In rat periodontal tissue, NaHS and LPS had an additive effect on osteoclast differentiation through activation of the TLR4 pathway but not the TLR2 pathway.</description><identifier>ISSN: 0022-3492</identifier><identifier>EISSN: 1943-3670</identifier><identifier>DOI: 10.1902/jop.2011.110315</identifier><identifier>PMID: 21910595</identifier><language>eng</language><publisher>Chicago, IL: American Academy of Periodontology</publisher><subject>Acid Phosphatase - analysis ; Animals ; Biological and medical sciences ; Biomarkers - analysis ; Blotting, Western ; Cell Count ; Cell Differentiation - drug effects ; Dentistry ; Gingiva - drug effects ; HMGB1 Protein - drug effects ; Hydrogen sulfide ; Hydrogen Sulfide - pharmacology ; Isoenzymes - analysis ; lipopolysaccharides ; Lipopolysaccharides - pharmacology ; Male ; Medical sciences ; osteoclasts ; Osteoclasts - drug effects ; Otorhinolaryngology. Stomatology ; Periodontium - cytology ; Periodontium - drug effects ; Porphyromonas gingivalis ; RANK Ligand - drug effects ; Rats ; Rats, Wistar ; Tartrate-Resistant Acid Phosphatase ; Toll-Like Receptor 2 - drug effects ; Toll-Like Receptor 4 - drug effects ; toll‐like receptor 2 ; toll‐like receptor 4 ; Tumor Necrosis Factor-alpha - drug effects</subject><ispartof>Journal of periodontology (1970), 2012-04, Vol.83 (4), p.522-527</ispartof><rights>2012 American Academy of Periodontology</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4382-d3d4f487b6c8c1987ad2f57ba29eb806bfb92726883b85395430ef2bf8c0b6313</citedby><cites>FETCH-LOGICAL-c4382-d3d4f487b6c8c1987ad2f57ba29eb806bfb92726883b85395430ef2bf8c0b6313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1902%2Fjop.2011.110315$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1902%2Fjop.2011.110315$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=25754555$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21910595$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Irie, Koichiro</creatorcontrib><creatorcontrib>Ekuni, Daisuke</creatorcontrib><creatorcontrib>Tomofuji, Takaaki</creatorcontrib><creatorcontrib>Endo, Yasumasa</creatorcontrib><creatorcontrib>Kasuyama, Kenta</creatorcontrib><creatorcontrib>Yaegaki, Ken</creatorcontrib><creatorcontrib>Morita, Manabu</creatorcontrib><title>Combined Effects of Hydrogen Sulfide and Lipopolysaccharide on Osteoclast Differentiation in Rats</title><title>Journal of periodontology (1970)</title><addtitle>J Periodontol</addtitle><description>Background: Lipopolysaccharide (LPS) stimulates osteoclast differentiation through toll‐like receptors (TLRs) 2 and 4, and hydrogen sulfide (H2S) induces osteoclast differentiation. If H2S activates TLRs, H2S may enhance the effects of LPS on osteoclast differentiation. The purpose of the present study is to examine the combined effects of sodium hydrogen sulfide (NaHS, an H2S donor drug) and LPS on osteoclast differentiation and TLR expression in rat periodontal tissue. Methods: Twenty‐eight male Wistar rats (8 weeks old) were divided into four groups (n = 7 per group): a control (no treatment) group and three experimental groups (NaHS group, LPS group, and a combination [NaHS + LPS] group). At 1 day after topical application of NaHS and/or Porphyromonas gingivalis LPS into the gingival sulcus of first molars, the number of tartrate‐resistant acid phosphate (TRAP)‐positive osteoclasts in the periodontal tissue was counted. Expression of TLR2 and TLR4 mRNAs and proteins in the gingival was also assessed. Results: The number of TRAP‐positive osteoclasts was significantly higher in the combination group than in any other group (P &lt;0.01). The combination group had 11.0‐fold higher TLR4 mRNA levels than the control group. TLR4 protein levels were also higher in the combination group than in the NaHS or LPS group. However, the TLR2 mRNA and protein levels were not significantly different in the combination group and the LPS group. Conclusion: In rat periodontal tissue, NaHS and LPS had an additive effect on osteoclast differentiation through activation of the TLR4 pathway but not the TLR2 pathway.</description><subject>Acid Phosphatase - analysis</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - analysis</subject><subject>Blotting, Western</subject><subject>Cell Count</subject><subject>Cell Differentiation - drug effects</subject><subject>Dentistry</subject><subject>Gingiva - drug effects</subject><subject>HMGB1 Protein - drug effects</subject><subject>Hydrogen sulfide</subject><subject>Hydrogen Sulfide - pharmacology</subject><subject>Isoenzymes - analysis</subject><subject>lipopolysaccharides</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>osteoclasts</subject><subject>Osteoclasts - drug effects</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Periodontium - cytology</subject><subject>Periodontium - drug effects</subject><subject>Porphyromonas gingivalis</subject><subject>RANK Ligand - drug effects</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Tartrate-Resistant Acid Phosphatase</subject><subject>Toll-Like Receptor 2 - drug effects</subject><subject>Toll-Like Receptor 4 - drug effects</subject><subject>toll‐like receptor 2</subject><subject>toll‐like receptor 4</subject><subject>Tumor Necrosis Factor-alpha - drug effects</subject><issn>0022-3492</issn><issn>1943-3670</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkLtPwzAQhy0EgvKY2ZAXxJTiZ2KPqBQKqgTiMVu2Y4NRGgc7Fep_T6oWGJms8333O90HwClGYywRufyI3ZggjMcYI4r5DhhhyWhBywrtghFChBSUSXIADnP-GErMKNoHBwRLjLjkI6AncWFC62o49d7ZPsPo4WxVp_jmWvi8bHyoHdRtDeehi11sVllb-67T-ju28CH3LtpG5x5ehyEhubYPug9DK7TwSff5GOx53WR3sn2PwOvN9GUyK-YPt3eTq3lhGRWkqGnNPBOVKa2wWIpK18TzymginRGoNN5IUpFSCGoEp5IPlzhPjBcWmZJiegQuNrldip9Ll3u1CNm6ptGti8usJBMSSVahgbzckDbFnJPzqkthodNKYaTWWtWgVa21qo3WYeJsm700C1f_8j8eB-B8C-hsdeOTbm3IfxyvOON8zfEN9xUat_pvr7p_nD4hTgj9BooIkKo</recordid><startdate>201204</startdate><enddate>201204</enddate><creator>Irie, Koichiro</creator><creator>Ekuni, Daisuke</creator><creator>Tomofuji, Takaaki</creator><creator>Endo, Yasumasa</creator><creator>Kasuyama, Kenta</creator><creator>Yaegaki, Ken</creator><creator>Morita, Manabu</creator><general>American Academy of Periodontology</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>7X8</scope></search><sort><creationdate>201204</creationdate><title>Combined Effects of Hydrogen Sulfide and Lipopolysaccharide on Osteoclast Differentiation in Rats</title><author>Irie, Koichiro ; Ekuni, Daisuke ; Tomofuji, Takaaki ; Endo, Yasumasa ; Kasuyama, Kenta ; Yaegaki, Ken ; Morita, Manabu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4382-d3d4f487b6c8c1987ad2f57ba29eb806bfb92726883b85395430ef2bf8c0b6313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Acid Phosphatase - analysis</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - analysis</topic><topic>Blotting, Western</topic><topic>Cell Count</topic><topic>Cell Differentiation - drug effects</topic><topic>Dentistry</topic><topic>Gingiva - drug effects</topic><topic>HMGB1 Protein - drug effects</topic><topic>Hydrogen sulfide</topic><topic>Hydrogen Sulfide - pharmacology</topic><topic>Isoenzymes - analysis</topic><topic>lipopolysaccharides</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>osteoclasts</topic><topic>Osteoclasts - drug effects</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Periodontium - cytology</topic><topic>Periodontium - drug effects</topic><topic>Porphyromonas gingivalis</topic><topic>RANK Ligand - drug effects</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Tartrate-Resistant Acid Phosphatase</topic><topic>Toll-Like Receptor 2 - drug effects</topic><topic>Toll-Like Receptor 4 - drug effects</topic><topic>toll‐like receptor 2</topic><topic>toll‐like receptor 4</topic><topic>Tumor Necrosis Factor-alpha - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Irie, Koichiro</creatorcontrib><creatorcontrib>Ekuni, Daisuke</creatorcontrib><creatorcontrib>Tomofuji, Takaaki</creatorcontrib><creatorcontrib>Endo, Yasumasa</creatorcontrib><creatorcontrib>Kasuyama, Kenta</creatorcontrib><creatorcontrib>Yaegaki, Ken</creatorcontrib><creatorcontrib>Morita, Manabu</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>MEDLINE - Academic</collection><jtitle>Journal of periodontology (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Irie, Koichiro</au><au>Ekuni, Daisuke</au><au>Tomofuji, Takaaki</au><au>Endo, Yasumasa</au><au>Kasuyama, Kenta</au><au>Yaegaki, Ken</au><au>Morita, Manabu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combined Effects of Hydrogen Sulfide and Lipopolysaccharide on Osteoclast Differentiation in Rats</atitle><jtitle>Journal of periodontology (1970)</jtitle><addtitle>J Periodontol</addtitle><date>2012-04</date><risdate>2012</risdate><volume>83</volume><issue>4</issue><spage>522</spage><epage>527</epage><pages>522-527</pages><issn>0022-3492</issn><eissn>1943-3670</eissn><abstract>Background: Lipopolysaccharide (LPS) stimulates osteoclast differentiation through toll‐like receptors (TLRs) 2 and 4, and hydrogen sulfide (H2S) induces osteoclast differentiation. If H2S activates TLRs, H2S may enhance the effects of LPS on osteoclast differentiation. The purpose of the present study is to examine the combined effects of sodium hydrogen sulfide (NaHS, an H2S donor drug) and LPS on osteoclast differentiation and TLR expression in rat periodontal tissue. Methods: Twenty‐eight male Wistar rats (8 weeks old) were divided into four groups (n = 7 per group): a control (no treatment) group and three experimental groups (NaHS group, LPS group, and a combination [NaHS + LPS] group). At 1 day after topical application of NaHS and/or Porphyromonas gingivalis LPS into the gingival sulcus of first molars, the number of tartrate‐resistant acid phosphate (TRAP)‐positive osteoclasts in the periodontal tissue was counted. Expression of TLR2 and TLR4 mRNAs and proteins in the gingival was also assessed. Results: The number of TRAP‐positive osteoclasts was significantly higher in the combination group than in any other group (P &lt;0.01). The combination group had 11.0‐fold higher TLR4 mRNA levels than the control group. TLR4 protein levels were also higher in the combination group than in the NaHS or LPS group. However, the TLR2 mRNA and protein levels were not significantly different in the combination group and the LPS group. Conclusion: In rat periodontal tissue, NaHS and LPS had an additive effect on osteoclast differentiation through activation of the TLR4 pathway but not the TLR2 pathway.</abstract><cop>Chicago, IL</cop><pub>American Academy of Periodontology</pub><pmid>21910595</pmid><doi>10.1902/jop.2011.110315</doi><tpages>6</tpages></addata></record>
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subjects Acid Phosphatase - analysis
Animals
Biological and medical sciences
Biomarkers - analysis
Blotting, Western
Cell Count
Cell Differentiation - drug effects
Dentistry
Gingiva - drug effects
HMGB1 Protein - drug effects
Hydrogen sulfide
Hydrogen Sulfide - pharmacology
Isoenzymes - analysis
lipopolysaccharides
Lipopolysaccharides - pharmacology
Male
Medical sciences
osteoclasts
Osteoclasts - drug effects
Otorhinolaryngology. Stomatology
Periodontium - cytology
Periodontium - drug effects
Porphyromonas gingivalis
RANK Ligand - drug effects
Rats
Rats, Wistar
Tartrate-Resistant Acid Phosphatase
Toll-Like Receptor 2 - drug effects
Toll-Like Receptor 4 - drug effects
toll‐like receptor 2
toll‐like receptor 4
Tumor Necrosis Factor-alpha - drug effects
title Combined Effects of Hydrogen Sulfide and Lipopolysaccharide on Osteoclast Differentiation in Rats
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