Laboratory of Immunopharmacology and Molecular Biology, São Francisco University Medical School (USF), Bragança Paulista, São Paulo 12916-900, Brazil.
Laboratory of Cell and Molecular Tumor Biology and Bioactive Compounds, São Francisco University Medical School (USF), Bragança Paulista, São Paulo 12916-900, Brazil.
Int J Mol Sci. 2023 Feb 14;24(4):3839. doi: 10.3390/ijms24043839.
Wound healing is characterized by a systemic and complex process of cellular and molecular activities. Dipotassium Glycyrrhizinate (DPG), a side product derived from glycyrrhizic acid, has several biological effects, such as being antiallergic, antioxidant, antibacterial, antiviral, gastroprotective, antitumoral, and anti-inflammatory. This study aimed to evaluate the anti-inflammatory effect of topical DPG on the healing of cutaneous wounds by secondary intention in an in vivo experimental model. Twenty-four male Wistar rats were used in the experiment, and were randomly divided into six groups of four. Circular excisions were performed and topically treated for 14 days after wound induction. Macroscopic and histopathological analyses were performed. Gene expression was evaluated by real-time qPCR. Our results showed that treatment with DPG caused a decrease in the inflammatory exudate as well as an absence of active hyperemia. Increases in granulation tissue, tissue reepithelization, and total collagen were also observed. Furthermore, DPG treatment reduced the expression of pro-inflammatory cytokines (, , , , , and ) while increasing the expression of , demonstrating anti-inflammatory effects across all three treatment periods. Based on our results, we conclude that DPG attenuates the inflammatory process by promoting skin wound healing through the modulation of distinct mechanisms and signaling pathways, including anti-inflammatory ones. This involves modulation of the expression of pro- and anti-inflammatory cytokine expression; promotion of new granulation tissue; angiogenesis; and tissue re-epithelialization, all of which contribute to tissue remodeling.
伤口愈合的特征是细胞和分子活动的全身性和复杂过程。甘草酸二钾(DPG)是甘草酸的副产物,具有多种生物学作用,如抗过敏、抗氧化、抗菌、抗病毒、胃保护、抗肿瘤和抗炎。本研究旨在评估局部 DPG 对二次愈合的皮肤伤口愈合的抗炎作用的体内实验模型。实验使用了 24 只雄性 Wistar 大鼠,随机分为六组,每组 4 只。在诱导伤口后进行 14 天的圆形切除和局部治疗。进行宏观和组织病理学分析。通过实时 qPCR 评估基因表达。我们的结果表明,DPG 治疗可减少炎症渗出物并消除活跃性充血。还观察到肉芽组织、组织再上皮化和总胶原的增加。此外,DPG 治疗减少了促炎细胞因子( 、 、 、 、 和 )的表达,同时增加了 的表达,表明在所有三个治疗期均具有抗炎作用。基于我们的结果,我们得出结论,DPG 通过调节不同的机制和信号通路,包括抗炎机制,来减轻炎症过程,从而促进皮肤伤口愈合。这涉及到促炎和抗炎细胞因子表达的调节;促进新的肉芽组织形成;血管生成;和组织再上皮化,所有这些都有助于组织重塑。