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Evaluation of Wound Healing Activity of Salvia haenkei Hydroalcoholic Aerial Part Extract on in vitro and in vivo Experimental Models

机译:体外和体内实验模型对丹参的伤口愈合活动评价

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Purpose: The aim of the present study was to evaluate the potential wound healing activity of the hydroalcoholic extract of Salvia haenkei on in vitro and in vivo experimental models. Materials and Methods: Preliminary analytical characterization of the hydroalcoholic extract of Salvia haenkei was made by reversed-phase high performance liquid chromatography (RP-HPLC) that permitted identification of a qualitative fingerprint of the extract of aerial parts. The wound healing activity of the hydroalcoholic extract of Salvia haenkei was evaluated in vitro by the scratch assay on human dermal fibroblasts and human epidermal keratinocytes and in vivo by standardized mouse excisional splinting model. Real-time PCR (RT-PCR) experiments were performed to analyze gene expression levels of inflammatory markers. Results: The scratch assay tests showed that the treatment with the hydroalcoholic extract of Salvia haenkei did not induce an increase in the fibroblasts migration rate with respect to the positive control. Instead, the hydroalcoholic extract of Salvia haenkei was effective in improving the wound closure rate on keratinocyte cell cultures with an almost total invasion of the scratch after 48 h of treatment; whereas the positive control, at the same time point, showed only a 67% reduction of the wound size. In vivo experiments showed that the groups treated with the extract of Salvia haenkei completely re-epithelized the wound in 2.7 days, a timing that was comparable with the action of the positive control that took only 2.1 days. Gene expression analysis showed that Salvia haenkei positively regulated the signaling pathway of the nuclear factor-κB (NF-κB) transcription factor. Conclusion: The results suggested that the hydroalcoholic extract of Salvia haenkei induced a clear wound healing effect.
机译:目的:本研究的目的是评估体外和体内实验模型的丹参醇提取物的潜在伤口愈合活性。材料和方法:通过反相高效液相色谱(RP-HPLC)制备了丹参的水醇提取物的初步分析表征,允许识别空中零件提取物的定性指纹。通过标准化小鼠切除夹板模型,在人类皮肤成纤维细胞和人表皮角质细胞和体内进行划痕测定,在体外评估丹参的伤口愈合液的伤口愈合活性。进行实时PCR(RT-PCR)实验以分析炎症标志物的基因表达水平。结果:划痕测定试验表明,丹参的水醇提取物治疗不引起相对于阳性对照的成纤维细胞迁移率的增加。相反,Salvia Heenkei的水醇提取物有效改善角质形成细胞培养物对角质形成细胞培养物的伤口闭合速率,并且在48小时后几乎完全侵袭划痕;虽然在同一时间点,阳性对照显示伤口尺寸的减少67%。在体内实验表明,用丹参提取物治疗的群体在2.7天内将伤口完全重新加工,其与仅服用2.1天的阳性对照的作用相当的时间。基因表达分析表明,Salvia Heenkei呈正调节核因子-κB(NF-κB)转录因子的信号通路。结论:结果表明,丹参的水醇提取物诱导了透明伤口愈合效果。

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