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Int J Clin Exp Pathol ; 8(6): 6692-9, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26261551

RESUMO

Excessive extracellular matrix degradation caused by the hyperfunction of matrix metalloproteinases (MMPs) has been implicated in the failure of pressure ulcers healing. EMMPRIN, as a widely expressed protein, has emerged as an important regulator of MMP activity. We hypothesize that EMMPRIN affects the process of pressure ulcer healing by modulating MMP activity. In the rat pressure ulcer model, the expression of EMMPRIN in ulcers detected by Western blot was elevated compared with that observed in normal tissue. To investigate the role of EMMPRIN in regulating ulcer healing, specific antibodies against EMMPRIN were used via direct administration on the pressure ulcer. Local blockage of EMMPRIN resulted in a poor ulcer healing process compared with control ulcers, which was the opposite of our expectation. Furthermore, inhibiting EMMPRIN minimally impacted MMP activity. However, the collagen content in the pressure ulcer was reduced in the EMMPRIN treated group. Angiogenesis and the expression of angiogenic factors in pressure ulcers were also reduced by EMMPRIN local blockage. The results in the present study indicate a novel effect of EMMPRIN in the regulation of pressure ulcer healing by controlling the collagen contents and angiogenesis rather than MMPs activity.


Assuntos
Anticorpos/farmacologia , Proteínas Sanguíneas/antagonistas & inibidores , Úlcera por Pressão/metabolismo , Pele/efeitos dos fármacos , Cicatrização/efeitos dos fármacos , Proteínas Angiogênicas/metabolismo , Animais , Basigina/imunologia , Basigina/metabolismo , Proteínas Sanguíneas/imunologia , Proteínas Sanguíneas/metabolismo , Colágeno/metabolismo , Modelos Animais de Doenças , Masculino , Metaloproteinase 2 da Matriz/metabolismo , Metaloproteinase 9 da Matriz/metabolismo , Neovascularização Fisiológica , Úlcera por Pressão/imunologia , Úlcera por Pressão/patologia , Ratos Sprague-Dawley , Pele/irrigação sanguínea , Pele/imunologia , Pele/metabolismo , Pele/patologia , Fatores de Tempo
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