Ebeling Sandra, Naumann Katrin, Pollok Simone, Wardecki Tina, Vidal-Y-Sy Sabine, Nascimento Juliana M, Boerries Melanie, Schmidt Gudula, Brandner Johanna M, Merfort Irmgard
Pharmaceutical Biology and Biotechnology, Albert-Ludwigs-University Freiburg, Freiburg, Germany.
Department of Dermatology and Venerology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.
PLoS One. 2014 Jan 22;9(1):e86147. doi: 10.1371/journal.pone.0086147. eCollection 2014.
Birch bark has a long lasting history as a traditional medicinal remedy to accelerate wound healing. Recently, the efficacy of birch bark preparations has also been proven clinically. As active principle pentacyclic triterpenes are generally accepted. Here, we report a comprehensive study on the underlying molecular mechanisms of the wound healing properties of a well-defined birch bark preparation named as TE (triterpene extract) as well as the isolated single triterpenes in human primary keratinocytes and porcine ex-vivo wound healing models.
METHODOLOGY/PRINCIPAL FINDINGS: We show positive wound healing effects of TE and betulin in scratch assay experiments with primary human keratinocytes and in a porcine ex-vivo wound healing model (WHM). Mechanistical studies elucidate that TE and betulin transiently upregulate pro-inflammatory cytokines, chemokines and cyclooxygenase-2 on gene and protein level. For COX-2 and IL-6 this increase of mRNA is due to an mRNA stabilizing effect of TE and betulin, a process in which p38 MAPK and HuR are involved. TE promotes keratinocyte migration, putatively by increasing the formation of actin filopodia, lamellipodia and stress fibers. Detailed analyses show that the TE components betulin, lupeol and erythrodiol exert this effect even in nanomolar concentrations. Targeting the actin cytoskeleton is dependent on the activation of Rho GTPases.
CONCLUSION/SIGNIFICANCE: Our results provide insights to understand the molecular mechanism of the clinically proven wound healing effect of birch bark. TE and betulin address the inflammatory phase of wound healing by transient up-regulation of several pro-inflammatory mediators. Further, they enhance migration of keratinocytes, which is essential in the second phase of wound healing. Our results, together with the clinically proven efficacy, identify birch bark as the first medical plant with a high potential to improve wound healing, a field which urgently needs effective remedies.
桦树皮作为一种促进伤口愈合的传统药物已有悠久历史。最近,桦树皮制剂的功效也已在临床上得到证实。五环三萜类化合物被普遍认为是其活性成分。在此,我们报告了一项关于一种名为TE(三萜提取物)的明确桦树皮制剂以及分离出的单一三萜类化合物在人原代角质形成细胞和猪离体伤口愈合模型中促进伤口愈合特性的潜在分子机制的综合研究。
方法/主要发现:我们在原代人角质形成细胞的划痕试验以及猪离体伤口愈合模型(WHM)中显示了TE和桦木醇的积极伤口愈合效果。机制研究表明,TE和桦木醇在基因和蛋白质水平上短暂上调促炎细胞因子、趋化因子和环氧化酶-2。对于COX-2和IL-6,mRNA的这种增加是由于TE和桦木醇的mRNA稳定作用,这一过程涉及p38丝裂原活化蛋白激酶和HuR。TE促进角质形成细胞迁移,推测是通过增加肌动蛋白丝状伪足、片状伪足和应力纤维的形成来实现的。详细分析表明,TE成分桦木醇、羽扇豆醇和红没药醇即使在纳摩尔浓度下也能发挥这种作用。靶向肌动蛋白细胞骨架依赖于Rho GTP酶的激活。
结论/意义:我们的结果为理解桦树皮临床证实的伤口愈合效果的分子机制提供了见解。TE和桦木醇通过短暂上调几种促炎介质来应对伤口愈合的炎症阶段。此外,它们增强角质形成细胞的迁移,这在伤口愈合的第二阶段至关重要。我们的结果与临床证实的功效一起,确定桦树皮是第一种具有改善伤口愈合高潜力的药用植物,而这一领域迫切需要有效的治疗方法。