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1.
Microsc Res Tech ; 82(6): 689-695, 2019 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-30637849

RESUMO

Proteins with osteoinductive potential, especially recombinant human bone morphogenetic protein (rhBMP)-2, have large effects on cell growth and their differentiation. The aim of this study was to assess repair of bone defects in rat calvaria with different types of grafts associated with rhBMP-2, through immunohistochemistry and micro computed tomography (CT) analyses. A total of 35 male Wistar rats were selected, each weighing ~250 g, with a waiting period of 6 weeks from the creation of the defect to the sacrifice, and divided into five groups (n = 7): autograft plus 5 µg rhBMP-2 (AuG/BMP-2); allograft plus 5 µg rhBMP-2 (AlG/BMP-2); xenograft (heterologous) plus 5 µg rhBMP-2 (XeG/BMP-2); 5 µg rhBMP-2 (BMP-2) and the control group (n = 7). The micro CT reveal that all groups associating different bone grafts with BMP-2 showed increased bone formation compared to the control. The immunostaining show that osteocalcin and bone sialoprotein were higher in groups with BMP-2 than control group; BMP was high expressed in AuG/BMP-2, AlG/BMP-2, and BMP-2; vascular endothelial growth factor (VEGF) was more expressed in groups with BMP-2; VEGF-R2 was low to moderate in AuG/BMP-2, XeG/BMP-2, and BMP-2, predominantly moderate in AlG/BMP-2 and low in the control; CD-31 was predominantly moderate in AuG/BMP-2, AlG/BMP-2, and XeG/BMP-2, low to moderate in BMP-2 and low in the control. The results revealed that rhBMP-2 improved bone repair when administered alone, or when associated with different bone grafts.


Assuntos
Proteína Morfogenética Óssea 2/administração & dosagem , Transplante Ósseo/métodos , Proteínas Recombinantes/administração & dosagem , Crânio/lesões , Animais , Modelos Animais de Doenças , Humanos , Imuno-Histoquímica , Sialoproteína de Ligação à Integrina/análise , Masculino , Osteocalcina/análise , Ligação Proteica , Ratos Wistar , Tomografia Computadorizada por Raios X , Transplante Autólogo/métodos , Transplante Heterólogo/métodos , Transplante Homólogo/métodos , Resultado do Tratamento
2.
Biomed Mater ; 13(2): 025022, 2018 02 08.
Artigo em Inglês | MEDLINE | ID: mdl-29053112

RESUMO

Bone grafts are used in the medical-surgical field for anatomical and functional reconstruction of lost bone areas, aiding the bone repair process by osteogenesis, osteinduction and osteoconduction. New materials such as F1 (fraction 1) protein extracted from the rubber tree Hevea brasiliensis have been investigated and currently present important properties for tissue repair, and are associated with neoangiogenesis, promoting cell adhesion and extracellular matrix formation. The main objective of this study was to investigate the association of F1 protein to different bone grafts in the repair of critical bone defects in the calvaria of Wistar rats. A total of 112 Wistar rats were divided as follows: autograft (AuG), allograft (AlG), xenograft (XeG), autograft/F1 (AuG-F1), allograft/F1 (AlG-F1), xenograft/F1 (XeG-F1), F1 (F1), control (CTL), with a waiting period of 4 and 6 weeks (w). The stereological AuG, AlG, AuG-F1 and AlG-F1 results had greater bone neoformation (p < 0.05). For immunohistochemistry, the angiogenic and osteogenic factors were higher for AuG-F1 and AlG-F1. TRAP-positive cells were higher in XeG-F1 and AlG (37 ± 9.53, 13.3 ± 4.16) (4 w) and XeG, AlG-F1 and XeG-F1 (20.33 ± 7.37; 15.25 ± 6.02, 19.33 ± 3.21) (6 w). For zymography, F1 showed increased gelatinolytic activity of MMP-2 and -9. It was concluded that the bone graft associated or not with F1 increases the angiogenic and osteogenic, biochemical and stereological factors.


Assuntos
Regeneração Óssea , Transplante Ósseo/métodos , Látex/uso terapêutico , Animais , Adesão Celular , Matriz Extracelular , Xenoenxertos , Hevea , Imuno-Histoquímica , Látex/química , Masculino , Metaloproteinase 2 da Matriz/metabolismo , Metaloproteinase 9 da Matriz/metabolismo , Osteogênese/efeitos dos fármacos , Peroxidases/química , Ratos , Ratos Wistar , Crânio/efeitos dos fármacos , Transplante Autólogo , Transplante Homólogo , Fator A de Crescimento do Endotélio Vascular
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