Effects of the cathepsin K inhibitor with mineral trioxide aggregate cements on osteoclastic activity
Objectives: Root resorption is an unexpected complication after replantation procedures. Combining anti-osteoclastic medicaments with retrograde root filling materials may avert this resorptive activity. The purpose of this study was to assess effects of a cathepsin K inhibitor with calcium silicate...
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Veröffentlicht in: | Restorative dentistry & endodontics 2019, Vol.44 (2), p.17.1-17.10 |
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creator | Kim, Hee-Sun Kim, Soojung Ko, Hyunjung Song, Minju Kim, Miri |
description | Objectives: Root resorption is an unexpected complication after replantation procedures. Combining anti-osteoclastic medicaments with retrograde root filling materials may avert this resorptive activity. The purpose of this study was to assess effects of a cathepsin K inhibitor with calcium silicate-based cements on osteoclastic activity. Methods: MC3T3-E1 cells were cultured for biocompatibility analyses. RAW 264.7 cells were cultured in the presence of the receptor activator of nuclear factor-kappa B and lipopolysaccharide, followed by treatment with Biodentine (BIOD) or ProRoot MTA with or without medicaments (Odanacatib [ODN], a cathepsin inhibitor and alendronate, a bisphosphonate). After drug treatment, the cell counting kit-8 assay and Alizarin red staining were performed to evaluate biocompatibility in MC3T3-E1 cells. Reverse-transcription polymerase chain reaction, tartrate-resistant acid phosphatase (TRAP) staining and enzyme-linked immunosorbent assays were performed in RAW 264.7 cells to determine the expression levels of inflammatory cytokines, interleukin $(IL)-1{\beta}$, IL-6, tumor necrosis $factor-{\alpha}$ ($TNF-{\alpha}$) and prostaglandin E2 (PGE2). Data were analyzed by one-way analysis of variance and Tukey's post hoc test (p < 0.05). Results: Biocompatibility results showed that there were no significant differences among any of the groups. RAW 264.7 cells treated with BIOD and ODN showed the lowest levels of $TNF-{\alpha}$ and PGE2. Treatments with BIOD + ODN were more potent suppressors of inflammatory cytokine expression (p < 0.05). Conclusion: The cathepsin K inhibitor with calcium silicate-based cement inhibits osteoclastic activity. This may have clinical application in preventing inflammatory root resorption in replanted teeth. |
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Combining anti-osteoclastic medicaments with retrograde root filling materials may avert this resorptive activity. The purpose of this study was to assess effects of a cathepsin K inhibitor with calcium silicate-based cements on osteoclastic activity. Methods: MC3T3-E1 cells were cultured for biocompatibility analyses. RAW 264.7 cells were cultured in the presence of the receptor activator of nuclear factor-kappa B and lipopolysaccharide, followed by treatment with Biodentine (BIOD) or ProRoot MTA with or without medicaments (Odanacatib [ODN], a cathepsin inhibitor and alendronate, a bisphosphonate). After drug treatment, the cell counting kit-8 assay and Alizarin red staining were performed to evaluate biocompatibility in MC3T3-E1 cells. Reverse-transcription polymerase chain reaction, tartrate-resistant acid phosphatase (TRAP) staining and enzyme-linked immunosorbent assays were performed in RAW 264.7 cells to determine the expression levels of inflammatory cytokines, interleukin $(IL)-1{\beta}$, IL-6, tumor necrosis $factor-{\alpha}$ ($TNF-{\alpha}$) and prostaglandin E2 (PGE2). Data were analyzed by one-way analysis of variance and Tukey's post hoc test (p < 0.05). Results: Biocompatibility results showed that there were no significant differences among any of the groups. RAW 264.7 cells treated with BIOD and ODN showed the lowest levels of $TNF-{\alpha}$ and PGE2. Treatments with BIOD + ODN were more potent suppressors of inflammatory cytokine expression (p < 0.05). Conclusion: The cathepsin K inhibitor with calcium silicate-based cement inhibits osteoclastic activity. This may have clinical application in preventing inflammatory root resorption in replanted teeth.</description><identifier>ISSN: 2234-7658</identifier><identifier>EISSN: 2234-7666</identifier><language>kor</language><ispartof>Restorative dentistry & endodontics, 2019, Vol.44 (2), p.17.1-17.10</ispartof><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>230,314,780,784,885,4024</link.rule.ids></links><search><creatorcontrib>Kim, Hee-Sun</creatorcontrib><creatorcontrib>Kim, Soojung</creatorcontrib><creatorcontrib>Ko, Hyunjung</creatorcontrib><creatorcontrib>Song, Minju</creatorcontrib><creatorcontrib>Kim, Miri</creatorcontrib><title>Effects of the cathepsin K inhibitor with mineral trioxide aggregate cements on osteoclastic activity</title><title>Restorative dentistry & endodontics</title><addtitle>RDE : Restorative dentistry & endodontics</addtitle><description>Objectives: Root resorption is an unexpected complication after replantation procedures. Combining anti-osteoclastic medicaments with retrograde root filling materials may avert this resorptive activity. The purpose of this study was to assess effects of a cathepsin K inhibitor with calcium silicate-based cements on osteoclastic activity. Methods: MC3T3-E1 cells were cultured for biocompatibility analyses. RAW 264.7 cells were cultured in the presence of the receptor activator of nuclear factor-kappa B and lipopolysaccharide, followed by treatment with Biodentine (BIOD) or ProRoot MTA with or without medicaments (Odanacatib [ODN], a cathepsin inhibitor and alendronate, a bisphosphonate). After drug treatment, the cell counting kit-8 assay and Alizarin red staining were performed to evaluate biocompatibility in MC3T3-E1 cells. Reverse-transcription polymerase chain reaction, tartrate-resistant acid phosphatase (TRAP) staining and enzyme-linked immunosorbent assays were performed in RAW 264.7 cells to determine the expression levels of inflammatory cytokines, interleukin $(IL)-1{\beta}$, IL-6, tumor necrosis $factor-{\alpha}$ ($TNF-{\alpha}$) and prostaglandin E2 (PGE2). Data were analyzed by one-way analysis of variance and Tukey's post hoc test (p < 0.05). Results: Biocompatibility results showed that there were no significant differences among any of the groups. RAW 264.7 cells treated with BIOD and ODN showed the lowest levels of $TNF-{\alpha}$ and PGE2. Treatments with BIOD + ODN were more potent suppressors of inflammatory cytokine expression (p < 0.05). Conclusion: The cathepsin K inhibitor with calcium silicate-based cement inhibits osteoclastic activity. This may have clinical application in preventing inflammatory root resorption in replanted teeth.</description><issn>2234-7658</issn><issn>2234-7666</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>JDI</sourceid><recordid>eNqNjr0KwkAQhA9RMKjvsI1lIF5iLpYiEdHCxj6c5yZZTO4kt_jz9kYQa5uZKb4ZZiACKeMkVGmaDn95mY3FzHs6R0millmsZCAwL0s07MGVwDWC0b3ePFk4ANmazsSugwdxDS1Z7HQD3JF70gVBV1WHlea-hS3az4gF5xmdabRnMqAN0534NRWjUjceZ1-fiPk2P2124ZV6rrAX3xT79eEoo8VK9t8iFasoyeJ_uTdTnUe8</recordid><startdate>2019</startdate><enddate>2019</enddate><creator>Kim, Hee-Sun</creator><creator>Kim, Soojung</creator><creator>Ko, Hyunjung</creator><creator>Song, Minju</creator><creator>Kim, Miri</creator><scope>JDI</scope></search><sort><creationdate>2019</creationdate><title>Effects of the cathepsin K inhibitor with mineral trioxide aggregate cements on osteoclastic activity</title><author>Kim, Hee-Sun ; Kim, Soojung ; Ko, Hyunjung ; Song, Minju ; Kim, Miri</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kisti_ndsl_JAKO2019247507370483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>kor</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Hee-Sun</creatorcontrib><creatorcontrib>Kim, Soojung</creatorcontrib><creatorcontrib>Ko, Hyunjung</creatorcontrib><creatorcontrib>Song, Minju</creatorcontrib><creatorcontrib>Kim, Miri</creatorcontrib><collection>KoreaScience</collection><jtitle>Restorative dentistry & endodontics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Hee-Sun</au><au>Kim, Soojung</au><au>Ko, Hyunjung</au><au>Song, Minju</au><au>Kim, Miri</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of the cathepsin K inhibitor with mineral trioxide aggregate cements on osteoclastic activity</atitle><jtitle>Restorative dentistry & endodontics</jtitle><addtitle>RDE : Restorative dentistry & endodontics</addtitle><date>2019</date><risdate>2019</risdate><volume>44</volume><issue>2</issue><spage>17.1</spage><epage>17.10</epage><pages>17.1-17.10</pages><issn>2234-7658</issn><eissn>2234-7666</eissn><abstract>Objectives: Root resorption is an unexpected complication after replantation procedures. Combining anti-osteoclastic medicaments with retrograde root filling materials may avert this resorptive activity. The purpose of this study was to assess effects of a cathepsin K inhibitor with calcium silicate-based cements on osteoclastic activity. Methods: MC3T3-E1 cells were cultured for biocompatibility analyses. RAW 264.7 cells were cultured in the presence of the receptor activator of nuclear factor-kappa B and lipopolysaccharide, followed by treatment with Biodentine (BIOD) or ProRoot MTA with or without medicaments (Odanacatib [ODN], a cathepsin inhibitor and alendronate, a bisphosphonate). After drug treatment, the cell counting kit-8 assay and Alizarin red staining were performed to evaluate biocompatibility in MC3T3-E1 cells. Reverse-transcription polymerase chain reaction, tartrate-resistant acid phosphatase (TRAP) staining and enzyme-linked immunosorbent assays were performed in RAW 264.7 cells to determine the expression levels of inflammatory cytokines, interleukin $(IL)-1{\beta}$, IL-6, tumor necrosis $factor-{\alpha}$ ($TNF-{\alpha}$) and prostaglandin E2 (PGE2). Data were analyzed by one-way analysis of variance and Tukey's post hoc test (p < 0.05). Results: Biocompatibility results showed that there were no significant differences among any of the groups. RAW 264.7 cells treated with BIOD and ODN showed the lowest levels of $TNF-{\alpha}$ and PGE2. Treatments with BIOD + ODN were more potent suppressors of inflammatory cytokine expression (p < 0.05). Conclusion: The cathepsin K inhibitor with calcium silicate-based cement inhibits osteoclastic activity. This may have clinical application in preventing inflammatory root resorption in replanted teeth.</abstract><oa>free_for_read</oa></addata></record> |
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title | Effects of the cathepsin K inhibitor with mineral trioxide aggregate cements on osteoclastic activity |
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