硫酸软骨素和硫酸氨基葡萄糖对小鼠和鸡胚绒毛膜尿囊膜血管网络的促血管生成活性测定

Fernanda Katharine de Souza Lins Borba, Edbhergue Ventura Lola Costa, Viviane Aparecida Balvedi Polli, Daniela Sousa Coelho, M. Maraschin, Paulo Fernando Dias, Romildo Albuquerque Nogueira
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引用次数: 2

摘要

目的:研究硫酸软骨素(CS)和硫酸氨基葡萄糖(GS)在体外诱导血管生成的能力。方法:通过鸡胚毛囊尿囊膜(CAM)和小鼠背侧皮肤血管形成实验,分析化合物的促血管生成活性,并对人脐静脉内皮细胞(HUVEC)进行细胞活力实验。结果:在活力测定中,浓度在30 ~ 3000 μg/ml范围内,HUVEC活菌数降低。在CAM实验中,与对照(磷酸盐缓冲盐水- pbs)相比,CS和GS在2.0 mg/植入物中的用量增加了血管数量。在成年瑞士小鼠背侧皮肤血管化实验中,给药组CS (2 mg/植入;明胶泡沫塞组血管数量增加(0.52±0.08 g/dl);以插头血红蛋白含量衡量),与成纤维细胞生长因子-2 (FGF-2;50 ng/植入)(0.53±0.1 g/dl)。而GS组对小鼠皮肤血管化无明显影响。结论:CS能促进CAM血管生成和背侧皮肤血管形成,而GS仅对CAM血管网络有促血管生成作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pro-angiogenic Activity Assay of Chondroitin Sulfate and Glucosamine Sulfate on Vascular Network of Mouse and of Chick Embryo Chorioallantoic Membrane
Objective: Target of this study was to test the capacity of chondroitin sulfate (CS) and glucosamine sulfate (GS) to induce in vivo angiogenesis. Methods: The proangiogenic activity of these compounds was analyzed through the assays in chorioallantoic membrane (CAM) of chick embryo and dorsal skin vascularization in mice, but before was realized a cell viability assay with human umbilical veins endothelial cells (HUVEC). Results: In the viability assay, concentrations tested between 30 and 3000 μg/ml showed a reduction of viable HUVEC number. In the CAM assay, CS and GS in an amount 2.0 mg/implant increased the vessels number as compared to control (phosphate buffered saline-PBS). In the assay of the dorsal skin vascularization of adult Swiss mice, the groups treated with CS (2 mg/implant; Gelfoam plug) exhibited an increase in the vessels number into plugs (0.52 ± 0.08 g/dl; measured as plug-hemoglobin content), a similar effect to that promoted by Fibroblast growth factor-2 (FGF-2; 50 ng/implant) (0.53 ± 0.1 g/dl). However the group treated with GS did not exhibit significant effect on mice skin vascularization. Conclusion: CS was capable to promote angiogenesis on CAM and dorsal skin vascularization, but GS only had pro-angiogenic activity in CAM vascular network.
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