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Combined effects of mineral trioxide aggregate and human placental extract on rat pulp tissue and growth, differentiation and angiogenesis in human dental pulp cells.
Chang, Seok-Woo; Kim, Ji-Youn; Kim, Mi-Joo; Kim, Ga-Hyun; Yi, Jin-Kyu; Lee, Deok-Won; Kum, Kee-Yeon; Kim, Eun-Cheol.
Afiliação
  • Chang SW; a Department of Conservative Dentistry ;
  • Kim JY; b Department of Oral and Maxillofacial Pathology and Research Center for Tooth and Periodontal Regeneration (MRC );
  • Kim MJ; b Department of Oral and Maxillofacial Pathology and Research Center for Tooth and Periodontal Regeneration (MRC );
  • Kim GH; b Department of Oral and Maxillofacial Pathology and Research Center for Tooth and Periodontal Regeneration (MRC );
  • Yi JK; a Department of Conservative Dentistry ;
  • Lee DW; c Department of Oral and Maxillofacial Surgery School of Dentistry , Kyung Hee University , Seoul , Republic of Korea ;
  • Kum KY; d Department of Conservative Dentistry , Seoul National University Dental Hospital , Seoul , Republic of Korea.
  • Kim EC; b Department of Oral and Maxillofacial Pathology and Research Center for Tooth and Periodontal Regeneration (MRC );
Acta Odontol Scand ; 74(4): 298-306, 2016.
Article em En | MEDLINE | ID: mdl-26807656
OBJECTIVE: The aim of this study was to evaluate the combined effects of mineral trioxide aggregate (MTA) and human placental extract (HPE) on cell growth, differentiation and in vitro angiogenesis of human dental pulp cells (HDPCs) and to identify underlying signal transduction mechanisms. In vivo dental pulp responses in rats for a pulp-capping agent were examined. MATERIALS AND METHODS: MTS assay. ALP activity test, alizarin red S staining and RT-PCR for marker genes were carried out to evaluate cell growth and differentiation. HUVEC migration, mRNA expression and capillary tube formation were measured to evaluate angiogenesis. Signal transduction was analysed using Western blotting and confocal microscopy. The pulps of rat maxillary first molars were exposed and capped with either MTA or MTA plus HPE. Histologic observation and scoring were performed. RESULTS: Compared to treatment of HDPCs with either HPE or MTA alone, the combination of HPE and MTA increased cell growth, ALP activity, mineralized nodules and expression of marker mRNAs. Combination HPE and MTA increased migration, capillary tube formation and angiogenic gene expression compared with MTA alone. Activation of Akt, mammalian target of rapamycin (mTOR), p38, JNK and ERK MAPK, Akt, and NF-κB were significantly increased by combining HPE and MTA compared with MTA alone. Pulp capping with MTA plus HPE in rats showed superior dentin bridge formation, odontoblastic layers and dentinal tubules and lower inflammatory cell response, compared to the MTA alone group. CONCLUSIONS: This study demonstrates for the first time that the use of MTA with HPE promotes cell growth, differentiation and angiogenesis in HDPCs, which were associated with mTOR, MAPK and NF-κB pathways. Direct pulp capping with HPE plus MTA showed superior results when compared with MTA alone. Thus, the combination of MTA and HPE may be useful for regenerative endodontics.
Assuntos
Compostos de Alumínio/farmacologia; Compostos de Cálcio/farmacologia; Polpa Dentária/efeitos dos fármacos; Óxidos/farmacologia; Extratos Placentários/farmacologia; Silicatos/farmacologia; Fosfatase Alcalina/efeitos dos fármacos; Compostos de Alumínio/uso terapêutico; Animais; Calcificação Fisiológica/efeitos dos fármacos; Compostos de Cálcio/uso terapêutico; Capilares/efeitos dos fármacos; Diferenciação Celular/efeitos dos fármacos; Linhagem Celular; Movimento Celular/efeitos dos fármacos; Proliferação de Células/efeitos dos fármacos; Polpa Dentária/irrigação sanguínea; Polpa Dentária/citologia; Dentina Secundária/efeitos dos fármacos; Combinação de Medicamentos; Células Endoteliais da Veia Umbilical Humana/efeitos dos fármacos; Humanos; MAP Quinase Quinase 4/efeitos dos fármacos; Sistema de Sinalização das MAP Quinases/efeitos dos fármacos; Masculino; Proteínas Quinases Ativadas por Mitógeno/efeitos dos fármacos; NF-kappa B/efeitos dos fármacos; Neovascularização Fisiológica/efeitos dos fármacos; Odontoblastos/citologia; Odontoblastos/efeitos dos fármacos; Óxidos/uso terapêutico; Extratos Placentários/uso terapêutico; Proteínas Proto-Oncogênicas c-akt/efeitos dos fármacos; Agentes de Capeamento da Polpa Dentária e Pulpectomia/uso terapêutico; Ratos; Ratos Sprague-Dawley; Transdução de Sinais/efeitos dos fármacos; Silicatos/uso terapêutico; Serina-Treonina Quinases TOR/efeitos dos fármacos; Proteínas Quinases p38 Ativadas por Mitógeno/efeitos dos fármacos
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Óxidos / Extratos Placentários / Silicatos / Compostos de Cálcio / Compostos de Alumínio / Polpa Dentária Tipo de estudo: Prognostic_studies Idioma: En Revista: Acta Odontol Scand Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Óxidos / Extratos Placentários / Silicatos / Compostos de Cálcio / Compostos de Alumínio / Polpa Dentária Tipo de estudo: Prognostic_studies Idioma: En Revista: Acta Odontol Scand Ano de publicação: 2016 Tipo de documento: Article