Immunolocalization of markers for bone formation during guided bone regeneration in osteopenic rats
Identifieur interne : 001A02 ( Main/Curation ); précédent : 001A01; suivant : 001A03Immunolocalization of markers for bone formation during guided bone regeneration in osteopenic rats
Auteurs : Tábata De Mello Tera [Brésil] ; Rodrigo Dias Nascimento [Brésil] ; Renata Falchete Do Prado [Brésil] ; Mauro Pedrine Santamaria [Brésil] ; Maria Aparecida Neves Jardini [Brésil]Source :
- Journal of Applied Oral Science [ 1678-7757 ] ; 2014.
Abstract
The aim of this paper was to evaluate the repair of onlay autogenous bone grafts covered or not covered by an expanded polytetrafluoroethylene (e-PTFE) membrane using immunohistochemistry in rats with induced estrogen deficiency.
Eighty female rats were randomly divided into two groups: ovariectomized (OVX) and with a simulation of the surgical procedure (SHAM). Each of these groups was again divided into groups with either placement of an autogenous bone graft alone (BG) or an autogenous bone graft associated with an e-PTFE membrane (BGM). Animals were euthanized on days 0, 7, 21, 45, and 60. The specimens were subjected to immunohistochemistry for bone sialoprotein (BSP), osteonectin (ONC), and osteocalcin (OCC).
All groups (OVX+BG, OVX+BMG, SHAM+BG, and SHAM+BMG) showed greater bone formation, observed between 7 and 21 days, when BSP and ONC staining were more intense. At the 45-day, the bone graft showed direct bonding to the recipient bed in all specimens. The ONC and OCC showed more expressed in granulation tissue, in the membrane groups, independently of estrogen deficiency.
The expression of bone forming markers was not negatively influenced by estrogen deficiency. However, the markers could be influenced by the presence of the e-PTFE membrane.
Url:
DOI: 10.1590/1678-775720140190
PubMed: 25591022
PubMed Central: 4307769
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Estadual Paulista − UNESP, São José dos Campos, SP, Brazil.</nlm:aff><country xml:lang="fr" wicri:curation="lc">Brésil</country><wicri:regionArea>- Department of Bioscience and Oral Diagnosis, Instituto de Ciência e Tecnologia − ICT, Univ. Estadual Paulista − UNESP, São José dos Campos, SP</wicri:regionArea><placeName><region type="state">État de São Paulo</region></placeName></affiliation></author><author><name sortKey="Nascimento, Rodrigo Dias" sort="Nascimento, Rodrigo Dias" uniqKey="Nascimento R" first="Rodrigo Dias" last="Nascimento">Rodrigo Dias Nascimento</name><affiliation wicri:level="2"><nlm:aff id="aff2">- Department of Diagnosis and Surgery, Instituto de Ciência e Tecnologia − ICT, Univ. Estadual Paulista − UNESP, São José dos Campos, SP, Brazil.</nlm:aff><country xml:lang="fr" wicri:curation="lc">Brésil</country><wicri:regionArea>- Department of Diagnosis and Surgery, Instituto de Ciência e Tecnologia − ICT, Univ. Estadual Paulista − UNESP, São José dos Campos, SP</wicri:regionArea><placeName><region type="state">État de São Paulo</region></placeName></affiliation></author><author><name sortKey="Do Prado, Renata Falchete" sort="Do Prado, Renata Falchete" uniqKey="Do Prado R" first="Renata Falchete" last="Do Prado">Renata Falchete Do Prado</name><affiliation wicri:level="2"><nlm:aff id="aff1">- Department of Bioscience and Oral Diagnosis, Instituto de Ciência e Tecnologia − ICT, Univ. Estadual Paulista − UNESP, São José dos Campos, SP, Brazil.</nlm:aff><country xml:lang="fr" wicri:curation="lc">Brésil</country><wicri:regionArea>- Department of Bioscience and Oral Diagnosis, Instituto de Ciência e Tecnologia − ICT, Univ. Estadual Paulista − UNESP, São José dos Campos, SP</wicri:regionArea><placeName><region type="state">État de São Paulo</region></placeName></affiliation></author><author><name sortKey="Santamaria, Mauro Pedrine" sort="Santamaria, Mauro Pedrine" uniqKey="Santamaria M" first="Mauro Pedrine" last="Santamaria">Mauro Pedrine Santamaria</name><affiliation wicri:level="2"><nlm:aff id="aff2">- Department of Diagnosis and Surgery, Instituto de Ciência e Tecnologia − ICT, Univ. Estadual Paulista − UNESP, São José dos Campos, SP, Brazil.</nlm:aff><country xml:lang="fr" wicri:curation="lc">Brésil</country><wicri:regionArea>- Department of Diagnosis and Surgery, Instituto de Ciência e Tecnologia − ICT, Univ. Estadual Paulista − UNESP, São José dos Campos, SP</wicri:regionArea><placeName><region type="state">État de São Paulo</region></placeName></affiliation></author><author><name sortKey="Jardini, Maria Aparecida Neves" sort="Jardini, Maria Aparecida Neves" uniqKey="Jardini M" first="Maria Aparecida Neves" last="Jardini">Maria Aparecida Neves Jardini</name><affiliation wicri:level="2"><nlm:aff id="aff2">- Department of Diagnosis and Surgery, Instituto de Ciência e Tecnologia − ICT, Univ. Estadual Paulista − UNESP, São José dos Campos, SP, Brazil.</nlm:aff><country xml:lang="fr" wicri:curation="lc">Brésil</country><wicri:regionArea>- Department of Diagnosis and Surgery, Instituto de Ciência e Tecnologia − ICT, Univ. Estadual Paulista − UNESP, São José dos Campos, SP</wicri:regionArea><placeName><region type="state">État de São Paulo</region></placeName></affiliation></author></analytic><series><title level="j">Journal of Applied Oral Science</title><idno type="ISSN">1678-7757</idno><idno type="eISSN">1678-7765</idno><imprint><date when="2014">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Objective</title><p> The aim of this paper was to evaluate the repair of onlay autogenous bone grafts covered or not covered by an expanded polytetrafluoroethylene (e-PTFE) membrane using immunohistochemistry in rats with induced estrogen deficiency.</p></sec><sec><title>Material and Methods</title><p> Eighty female rats were randomly divided into two groups: ovariectomized (OVX) and with a simulation of the surgical procedure (SHAM). Each of these groups was again divided into groups with either placement of an autogenous bone graft alone (BG) or an autogenous bone graft associated with an e-PTFE membrane (BGM). Animals were euthanized on days 0, 7, 21, 45, and 60. The specimens were subjected to immunohistochemistry for bone sialoprotein (BSP), osteonectin (ONC), and osteocalcin (OCC).</p></sec><sec><title>Results</title><p> All groups (OVX+BG, OVX+BMG, SHAM+BG, and SHAM+BMG) showed greater bone formation, observed between 7 and 21 days, when BSP and ONC staining were more intense. At the 45-day, the bone graft showed direct bonding to the recipient bed in all specimens. The ONC and OCC showed more expressed in granulation tissue, in the membrane groups, independently of estrogen deficiency.</p></sec><sec><title>Conclusions</title><p> The expression of bone forming markers was not negatively influenced by estrogen deficiency. However, the markers could be influenced by the presence of the e-PTFE membrane.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Adeyemo, Wl" uniqKey="Adeyemo W">WL Adeyemo</name></author><author><name sortKey="Reuther, T" uniqKey="Reuther T">T Reuther</name></author><author><name sortKey="Bloch, W" uniqKey="Bloch W">W Bloch</name></author><author><name sortKey="Korkmaz, Y" uniqKey="Korkmaz Y">Y Korkmaz</name></author><author><name sortKey="Fisher, Jh" uniqKey="Fisher J">JH Fisher</name></author><author><name sortKey="Zoller, Je" uniqKey="Zoller J">JE Zöller</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Arambawatta, Aks" uniqKey="Arambawatta A">AKS Arambawatta</name></author><author><name sortKey="Yamamoto, T" uniqKey="Yamamoto T">T Yamamoto</name></author><author><name sortKey="Wakita, M" uniqKey="Wakita M">M 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Nakadate</name></author><author><name sortKey="Ohnishi, H" uniqKey="Ohnishi H">H Ohnishi</name></author><author><name sortKey="Fujii, N" uniqKey="Fujii N">N Fujii</name></author><author><name sortKey="Oda, K" uniqKey="Oda K">K Oda</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Wronski, Tj" uniqKey="Wronski T">TJ Wronski</name></author><author><name sortKey="Cintr N, M" uniqKey="Cintr N M">M Cintrón</name></author><author><name sortKey="Dann, Lm" uniqKey="Dann L">LM Dann</name></author></analytic></biblStruct></listBibl></div1></back></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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|clé= PMC:4307769
|texte= Immunolocalization of markers for bone formation during guided bone regeneration in osteopenic rats
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