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[Effects of Xiaodu Yuji Paste on Protein Expressions of VEGF/SDF-1 a/CXCR4 in Granulation Tissue of Diabetic Foot Patients].
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 37(2): 165-168, 2017 Feb.
Article em Zh | MEDLINE | ID: mdl-30650267
ABSTRACT
Objective To observe the effects of Xiaodu Yuji Paste (XYP) on protein expressions of vascular endothelial growth factor (VEGF)/stromal cell derived factor la (SDF-1a)/chemokine recep- tor 4 (CXCR4) in granulation tissue of diabetic foot patients. Methods Totally 56 patients with diabetic foot were assigned to the control group (29 cases) and the treatment group (27 cases) according to Wagner grading method (the range and the degree of foot lesion). Patients in the control group received basic treatment (anti-inflammation, blood glucose control, anti-coagulation, debridement, drainage, and so on) for 8 weeks. Patients in the treatment group additionally received XYP for 8 weeks. The wound healing was observed. Contents and protein expressions of VEGF/SDF-1 a/CXCR4 were detected using SP method and Western blot. Results The wound healing rates after 2, 4, 8 weeks of treatment were signifi- cantly higher in the treatment group than in the control group (all P <0. 05). Contents and protein expres- sions of VEGF/SDF-1 a/CXCR4 protein expression at week 8 after treatment were all significantly higher in the treatment group than in the control group (P <0. 05). Conclusion The therapeutic effect of XYP might be associated with promoting expressions of VEGF/SDF-la/CXCR4, thus promoting angiogenesis and facilitating wound healing.
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Base de dados: MEDLINE Assunto principal: Medicamentos de Ervas Chinesas / Pé Diabético / Receptores CXCR4 / Fator A de Crescimento do Endotélio Vascular / Quimiocina CXCL12 Limite: Humans Idioma: Zh Ano de publicação: 2017 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Medicamentos de Ervas Chinesas / Pé Diabético / Receptores CXCR4 / Fator A de Crescimento do Endotélio Vascular / Quimiocina CXCL12 Limite: Humans Idioma: Zh Ano de publicação: 2017 Tipo de documento: Article