GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars

Abstract Introduction This study aimed to clarify pulpal responses to gallium-aluminum-arsenide (GaAlAs) laser irradiation. Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 day...

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Veröffentlicht in:Journal of endodontics 2011-08, Vol.37 (8), p.1086-1091
Hauptverfasser: Shigetani, Yoshimi, DDS, PhD, Sasa, Natsuki, DDS, Suzuki, Hironobu, DDS, PhD, Okiji, Takashi, DDS, PhD, Ohshima, Hayato, DDS, PhD
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container_end_page 1091
container_issue 8
container_start_page 1086
container_title Journal of endodontics
container_volume 37
creator Shigetani, Yoshimi, DDS, PhD
Sasa, Natsuki, DDS
Suzuki, Hironobu, DDS, PhD
Okiji, Takashi, DDS, PhD
Ohshima, Hayato, DDS, PhD
description Abstract Introduction This study aimed to clarify pulpal responses to gallium-aluminum-arsenide (GaAlAs) laser irradiation. Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 days. The demineralized paraffin sections were processed for immunohistochemistry for heat-shock protein (HSP)-25 and nestin in addition to cell proliferation assay using bromodeoxyuridine (BrdU) labeling and apoptosis assay using deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL). Results Intense HSP-25 and nestin immunoreactivities in the odontoblast layer were weakened immediately after 0.5-W irradiation and recovered on day 1, resulting in slight tertiary dentin formation by day 14. On the contrary, 1.5-W irradiation immediately induced the loss of HSP-25 and nestin-immunoreactivities in the odontoblast layer. On day 1, numerous TUNEL-positive cells appeared in a degenerative zone that was surrounded by intense HSP-25 immunoreactivity. BrdU-positive cells occurred within the intensely HSP-25–immunopositive areas during days 2 through 5, whereas TUNEL-positive cells gradually decreased in number by day 5. HSP-25– and nestin-positive odontoblast-like cells were arranged along the pulp-dentin border by day 7, resulting in remarkable tertiary dentin formation on day 14. Conclusions The output energy determined pulpal healing patterns after GaAlAs laser irradiation; the higher energy induced the apoptosis in the affected dental pulp including odontoblasts followed by active cell proliferation in the intense HSP-25–immunoreactive areas surrounding the degenerative tissue, resulting in abundant tertiary dentin formation. Thus, the optimal GaAlAs laser irradiation elicited intentional tertiary dentin formation in the dental pulp.
doi_str_mv 10.1016/j.joen.2011.05.020
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Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 days. The demineralized paraffin sections were processed for immunohistochemistry for heat-shock protein (HSP)-25 and nestin in addition to cell proliferation assay using bromodeoxyuridine (BrdU) labeling and apoptosis assay using deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL). Results Intense HSP-25 and nestin immunoreactivities in the odontoblast layer were weakened immediately after 0.5-W irradiation and recovered on day 1, resulting in slight tertiary dentin formation by day 14. On the contrary, 1.5-W irradiation immediately induced the loss of HSP-25 and nestin-immunoreactivities in the odontoblast layer. On day 1, numerous TUNEL-positive cells appeared in a degenerative zone that was surrounded by intense HSP-25 immunoreactivity. BrdU-positive cells occurred within the intensely HSP-25–immunopositive areas during days 2 through 5, whereas TUNEL-positive cells gradually decreased in number by day 5. HSP-25– and nestin-positive odontoblast-like cells were arranged along the pulp-dentin border by day 7, resulting in remarkable tertiary dentin formation on day 14. Conclusions The output energy determined pulpal healing patterns after GaAlAs laser irradiation; the higher energy induced the apoptosis in the affected dental pulp including odontoblasts followed by active cell proliferation in the intense HSP-25–immunoreactive areas surrounding the degenerative tissue, resulting in abundant tertiary dentin formation. Thus, the optimal GaAlAs laser irradiation elicited intentional tertiary dentin formation in the dental pulp.</description><identifier>ISSN: 0099-2399</identifier><identifier>EISSN: 1878-3554</identifier><identifier>DOI: 10.1016/j.joen.2011.05.020</identifier><identifier>PMID: 21763899</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Apoptosis ; Bromodeoxyuridine - metabolism ; Cell Proliferation ; dental pulp ; Dental Pulp - cytology ; Dental Pulp - physiology ; dentin ; Dentin, Secondary - secretion ; Dentistry ; Endocrinology &amp; Metabolism ; Female ; heat-shock proteins ; HSP27 Heat-Shock Proteins - biosynthesis ; In Situ Nick-End Labeling ; Intermediate Filament Proteins - biosynthesis ; laser ; Lasers, Semiconductor - adverse effects ; Molar ; Nerve Tissue Proteins - biosynthesis ; Nestin ; odontoblasts ; Odontoblasts - physiology ; Rats ; Rats, Wistar ; Wound Healing</subject><ispartof>Journal of endodontics, 2011-08, Vol.37 (8), p.1086-1091</ispartof><rights>American Association of Endodontists</rights><rights>2011 American Association of Endodontists</rights><rights>Copyright © 2011 American Association of Endodontists. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-dde95ffe20ccf6c9493baa23df4de19142eb1a2c9b27c04d1f64dc9e2a1c2e363</citedby><cites>FETCH-LOGICAL-c476t-dde95ffe20ccf6c9493baa23df4de19142eb1a2c9b27c04d1f64dc9e2a1c2e363</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.joen.2011.05.020$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3541,27915,27916,45986</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21763899$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shigetani, Yoshimi, DDS, PhD</creatorcontrib><creatorcontrib>Sasa, Natsuki, DDS</creatorcontrib><creatorcontrib>Suzuki, Hironobu, DDS, PhD</creatorcontrib><creatorcontrib>Okiji, Takashi, DDS, PhD</creatorcontrib><creatorcontrib>Ohshima, Hayato, DDS, PhD</creatorcontrib><title>GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars</title><title>Journal of endodontics</title><addtitle>J Endod</addtitle><description>Abstract Introduction This study aimed to clarify pulpal responses to gallium-aluminum-arsenide (GaAlAs) laser irradiation. Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 days. The demineralized paraffin sections were processed for immunohistochemistry for heat-shock protein (HSP)-25 and nestin in addition to cell proliferation assay using bromodeoxyuridine (BrdU) labeling and apoptosis assay using deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL). Results Intense HSP-25 and nestin immunoreactivities in the odontoblast layer were weakened immediately after 0.5-W irradiation and recovered on day 1, resulting in slight tertiary dentin formation by day 14. On the contrary, 1.5-W irradiation immediately induced the loss of HSP-25 and nestin-immunoreactivities in the odontoblast layer. On day 1, numerous TUNEL-positive cells appeared in a degenerative zone that was surrounded by intense HSP-25 immunoreactivity. BrdU-positive cells occurred within the intensely HSP-25–immunopositive areas during days 2 through 5, whereas TUNEL-positive cells gradually decreased in number by day 5. HSP-25– and nestin-positive odontoblast-like cells were arranged along the pulp-dentin border by day 7, resulting in remarkable tertiary dentin formation on day 14. Conclusions The output energy determined pulpal healing patterns after GaAlAs laser irradiation; the higher energy induced the apoptosis in the affected dental pulp including odontoblasts followed by active cell proliferation in the intense HSP-25–immunoreactive areas surrounding the degenerative tissue, resulting in abundant tertiary dentin formation. Thus, the optimal GaAlAs laser irradiation elicited intentional tertiary dentin formation in the dental pulp.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Bromodeoxyuridine - metabolism</subject><subject>Cell Proliferation</subject><subject>dental pulp</subject><subject>Dental Pulp - cytology</subject><subject>Dental Pulp - physiology</subject><subject>dentin</subject><subject>Dentin, Secondary - secretion</subject><subject>Dentistry</subject><subject>Endocrinology &amp; Metabolism</subject><subject>Female</subject><subject>heat-shock proteins</subject><subject>HSP27 Heat-Shock Proteins - biosynthesis</subject><subject>In Situ Nick-End Labeling</subject><subject>Intermediate Filament Proteins - biosynthesis</subject><subject>laser</subject><subject>Lasers, Semiconductor - adverse effects</subject><subject>Molar</subject><subject>Nerve Tissue Proteins - biosynthesis</subject><subject>Nestin</subject><subject>odontoblasts</subject><subject>Odontoblasts - physiology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Wound Healing</subject><issn>0099-2399</issn><issn>1878-3554</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2LFDEQhoMo7rj6BzxIbp66zUd_TECEYdZdB0ZcdD2HTFINaTNJm6QX9uB_N02vHjx4qsvzvlQ9hdBrSmpKaPdurMcAvmaE0pq0NWHkCdrQbb-teNs2T9GGECEqxoW4QC9SGgmhPef9c3TBaN_xrRAb9OtG7dwu4aNKEPEhRmWsyjZ4fPBm1pDwTmd7D_gOYrYqPuAr8Nl6fB3ieQXVkEv0dnaTcng3hSmHZBNW3uA9OIdvY3B2gLjSJfpVZfw5OBXTS_RsUC7Bq8d5ib5ff7zbf6qOX24O-92x0k3f5coYEO0wACNaD50WjeAnpRg3Q2OACtowOFHFtDixXpPG0KFrjBbAFNUMeMcv0du1d4rh5wwpy7NNuiynPIQ5yeKMMNH0opBsJXUMKUUY5BTtudwtKZGLdTnKxbpcrEvSymK9hN481s-nM5i_kT-aC_B-BaAceW8hyqQteA3GRtBZmmD_3__hn7h21lut3A94gDSGOfqiT1KZmCTy2_L35e2UEtLRpuW_Ad4Aqoo</recordid><startdate>20110801</startdate><enddate>20110801</enddate><creator>Shigetani, Yoshimi, DDS, PhD</creator><creator>Sasa, Natsuki, DDS</creator><creator>Suzuki, Hironobu, DDS, PhD</creator><creator>Okiji, Takashi, DDS, PhD</creator><creator>Ohshima, Hayato, DDS, PhD</creator><general>Elsevier Inc</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></search><sort><creationdate>20110801</creationdate><title>GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars</title><author>Shigetani, Yoshimi, DDS, PhD ; Sasa, Natsuki, DDS ; Suzuki, Hironobu, DDS, PhD ; Okiji, Takashi, DDS, PhD ; Ohshima, Hayato, DDS, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-dde95ffe20ccf6c9493baa23df4de19142eb1a2c9b27c04d1f64dc9e2a1c2e363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Bromodeoxyuridine - metabolism</topic><topic>Cell Proliferation</topic><topic>dental pulp</topic><topic>Dental Pulp - cytology</topic><topic>Dental Pulp - physiology</topic><topic>dentin</topic><topic>Dentin, Secondary - secretion</topic><topic>Dentistry</topic><topic>Endocrinology &amp; Metabolism</topic><topic>Female</topic><topic>heat-shock proteins</topic><topic>HSP27 Heat-Shock Proteins - biosynthesis</topic><topic>In Situ Nick-End Labeling</topic><topic>Intermediate Filament Proteins - biosynthesis</topic><topic>laser</topic><topic>Lasers, Semiconductor - adverse effects</topic><topic>Molar</topic><topic>Nerve Tissue Proteins - biosynthesis</topic><topic>Nestin</topic><topic>odontoblasts</topic><topic>Odontoblasts - physiology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Wound Healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shigetani, Yoshimi, DDS, PhD</creatorcontrib><creatorcontrib>Sasa, Natsuki, DDS</creatorcontrib><creatorcontrib>Suzuki, Hironobu, DDS, PhD</creatorcontrib><creatorcontrib>Okiji, Takashi, DDS, PhD</creatorcontrib><creatorcontrib>Ohshima, Hayato, DDS, PhD</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><jtitle>Journal of endodontics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shigetani, Yoshimi, DDS, PhD</au><au>Sasa, Natsuki, DDS</au><au>Suzuki, Hironobu, DDS, PhD</au><au>Okiji, Takashi, DDS, PhD</au><au>Ohshima, Hayato, DDS, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars</atitle><jtitle>Journal of endodontics</jtitle><addtitle>J Endod</addtitle><date>2011-08-01</date><risdate>2011</risdate><volume>37</volume><issue>8</issue><spage>1086</spage><epage>1091</epage><pages>1086-1091</pages><issn>0099-2399</issn><eissn>1878-3554</eissn><abstract>Abstract Introduction This study aimed to clarify pulpal responses to gallium-aluminum-arsenide (GaAlAs) laser irradiation. Methods Maxillary first molars of 8-week-old rats were irradiated at an output power of 0.5 or 1.5 W for 180 seconds, and the samples were collected at intervals of 0 to 14 days. The demineralized paraffin sections were processed for immunohistochemistry for heat-shock protein (HSP)-25 and nestin in addition to cell proliferation assay using bromodeoxyuridine (BrdU) labeling and apoptosis assay using deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL). Results Intense HSP-25 and nestin immunoreactivities in the odontoblast layer were weakened immediately after 0.5-W irradiation and recovered on day 1, resulting in slight tertiary dentin formation by day 14. On the contrary, 1.5-W irradiation immediately induced the loss of HSP-25 and nestin-immunoreactivities in the odontoblast layer. On day 1, numerous TUNEL-positive cells appeared in a degenerative zone that was surrounded by intense HSP-25 immunoreactivity. BrdU-positive cells occurred within the intensely HSP-25–immunopositive areas during days 2 through 5, whereas TUNEL-positive cells gradually decreased in number by day 5. HSP-25– and nestin-positive odontoblast-like cells were arranged along the pulp-dentin border by day 7, resulting in remarkable tertiary dentin formation on day 14. Conclusions The output energy determined pulpal healing patterns after GaAlAs laser irradiation; the higher energy induced the apoptosis in the affected dental pulp including odontoblasts followed by active cell proliferation in the intense HSP-25–immunoreactive areas surrounding the degenerative tissue, resulting in abundant tertiary dentin formation. Thus, the optimal GaAlAs laser irradiation elicited intentional tertiary dentin formation in the dental pulp.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21763899</pmid><doi>10.1016/j.joen.2011.05.020</doi><tpages>6</tpages></addata></record>
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subjects Animals
Apoptosis
Bromodeoxyuridine - metabolism
Cell Proliferation
dental pulp
Dental Pulp - cytology
Dental Pulp - physiology
dentin
Dentin, Secondary - secretion
Dentistry
Endocrinology & Metabolism
Female
heat-shock proteins
HSP27 Heat-Shock Proteins - biosynthesis
In Situ Nick-End Labeling
Intermediate Filament Proteins - biosynthesis
laser
Lasers, Semiconductor - adverse effects
Molar
Nerve Tissue Proteins - biosynthesis
Nestin
odontoblasts
Odontoblasts - physiology
Rats
Rats, Wistar
Wound Healing
title GaAlAs Laser Irradiation Induces Active Tertiary Dentin Formation after Pulpal Apoptosis and Cell Proliferation in Rat Molars
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