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Chinese Journal of Integrated Traditional and Western Medicine ; (12): 218-223, 2014.
Artigo em Chinês | WPRIM | ID: wpr-312841

RESUMO

<p><b>OBJECTIVE</b>To study the effect of Shengji Huayu Recipe (SHR)on the expression of MMP-3 and TIMP-1 in the skin ulcer tissue of diabetic rats.</p><p><b>METHODS</b>The skin ulcer model was established in diabetic mice. Different compatibility proportions of SHR [the ratio of Shengji Recipe (SJR) to Huayu Recipe (HYR) = 2:1, 1:1, and 1:2, respectively] were used to intervene. The expression of MMP-3 protein in the skin ulcer of diabetic rats was detected by Western blot method,and TIMP-1 protein was detected by immunohistochemical assay.</p><p><b>RESULTS</b>At each time point, there was no statistical difference in the blood glucose level among groups (P > 0.05). But all of them increased significantly,when compared with those of the normal wound group (P < 0.01). As for the difference between after would area treatment and before would area treatment, better effect was obtained in the SHR No. 3 group and the normal ulcer group than in the diabetic ulcer model group (P < 0.05). Results of Western blot showed that the MMP-3 protein expression was higher in the SHR No. 2 group than in the SHR No.3 group (P < 0.05). Immunohistochemical results showed that TIMP-1 protein expression was lower in the SHR No. 2 group than in the SHR No. 3 group and the diabetic ulcer model group (P < 0.05). TIMP-1 protein expression was higherin the SHR No. 3 group than in the SHR No. 2 group (P < 0.01).</p><p><b>CONCLUSION</b>Using SHR No.3 was conducive to the promotion of wound healing in early wound repair stage, and using SHR No. 2 might be conducive to inhibiting the formation of pathological scar.</p>


Assuntos
Animais , Masculino , Ratos , Diabetes Mellitus Experimental , Metabolismo , Medicamentos de Ervas Chinesas , Farmacologia , Usos Terapêuticos , Metaloproteinase 3 da Matriz , Metabolismo , Fitoterapia , Ratos Sprague-Dawley , Pele , Patologia , Úlcera Cutânea , Tratamento Farmacológico , Metabolismo , Inibidor Tecidual de Metaloproteinase-1 , Metabolismo
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