Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
1.
Acta cir. bras ; 34(1): e20190010000007, 2019. tab, graf
Artigo em Inglês | LILACS | ID: biblio-983684

RESUMO

Abstract Purpose: To investigate the impact of Ramipril (RAM) on the expressions of insulin-like growth factor-1 (IGF-1) and renal mesangial matrix (RMM) in rats with diabetic nephropathy (DN). Methods: The Sprague Dawley rats were divided into normal control (NC) group (n = 12), DN group (n = 11), and DN+RAM group (n = 12). The ratio of renal weight to body weight (RBT), fasting blood glucose (FBG), HbA1c, 24-h urine protein (TPU), blood urea nitrogen (BUN), creatinine (Cr), renal pathological changes, the levels of IGF-1, fibronectin (FN), type IV collagen (Col-IV), and matrix metalloproteinases (MMP)-2 were compared among the groups. Results: Compared with NC group, the RBT, FBG, HbA1c, TPU, BUN, Cr, and RMM in DN group were significantly increased (P < 0.05), the IGF-1, FN, and Col-IV were significantly upregulated (P < 0.05), while MMP was significantly downregulated (P < 0.05). Compared with DN group, the indexes except for the FBG and HbA1c in DN+RAM group were significantly improved (P < 0.05), among which IGF-1 exhibited significant positive correlation with TPU(r=0.937), FN(r=0.896) and Col-IV(r=0.871), while significant negative correlation with MMP-2 (r=-0.826) (P<0.05). Conclusion: RAM may protect the kidneys by suppressing IGF-1 and mitigating the accumulation of RMM.


Assuntos
Animais , Masculino , Ratos , Fator de Crescimento Insulin-Like I/antagonistas & inibidores , Inibidores da Enzima Conversora de Angiotensina/farmacologia , Ramipril/farmacologia , Nefropatias Diabéticas/tratamento farmacológico , Células Mesangiais/efeitos dos fármacos , Fator de Crescimento Insulin-Like I/metabolismo , Imuno-Histoquímica , Fibronectinas/efeitos dos fármacos , Fibronectinas/metabolismo , Ratos Sprague-Dawley , Metaloproteinases da Matriz/efeitos dos fármacos , Metaloproteinases da Matriz/metabolismo , Colágeno Tipo IV/efeitos adversos , Colágeno Tipo IV/metabolismo , Nefropatias Diabéticas/metabolismo , Células Mesangiais/metabolismo
2.
Artigo em Inglês | IMSEAR | ID: sea-139987

RESUMO

Context: Today many materials have been introduced for root-end filling materials. One of them is mineral trioxide aggregate (MTA) that is mentioned as a gold standard. Aims: The purpose of this in vitro study was to evaluate the reaction of human periodontal ligament fibroblasts to the root-end filling materials, such as ProRoot MTA, Portland cement, and amalgam. Settings and Design: Eight impacted teeth were extracted in aseptic condition. The tissues around the roots were used to obtain fibroblast cells. After cell proliferation, they were cultured in the chamber slides and the extracts of the materials were added to the wells. Materials and Methods: Immunocytochemical method for measuring the expression of Fibronectin, collagen I and transforming growth factor beta (TGF®) was performed by Olysia Bioreport Imaging Software. Statistical Analysis Used: The results were analyzed by SPSS 13.0 and Tukey post hoc test with P<0.05 as the limit of significance. Results: Collagen expression in MTA specimens was higher than the other groups in 24 h significantly. After 48 h, the Portland cement group showed the most expression of collagen significantly and after 1 week, Portland cement and MTA groups had the most expression of collagen but there was no significant difference between these 2 groups. After 1 week, the Portland cement group demonstrated a higher amount of TGF® and fibronectin. Conclusions: The results suggest that Portland cement can be used as a less expensive root filling material with low toxicity. It has better effects than amalgam on the fibroblasts.


Assuntos
Compostos de Alumínio/farmacologia , Compostos de Cálcio/farmacologia , Técnicas de Cultura de Células , Células Cultivadas , Colágeno Tipo I/análise , Colágeno Tipo I/efeitos dos fármacos , Corantes/diagnóstico , Amálgama Dentário/farmacologia , Cimentos Dentários/farmacologia , Combinação de Medicamentos , Fibroblastos/efeitos dos fármacos , Fibronectinas/análise , Fibronectinas/efeitos dos fármacos , Humanos , Processamento de Imagem Assistida por Computador , Imuno-Histoquímica , Teste de Materiais , Óxidos/farmacologia , Ligamento Periodontal/efeitos dos fármacos , Obturação Retrógrada , Materiais Restauradores do Canal Radicular/farmacologia , Silicatos/farmacologia , Fatores de Tempo , Fator de Crescimento Transformador beta/análise , Fator de Crescimento Transformador beta/efeitos dos fármacos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA