[通草洗剂通过下调炎症因子和抑制炎症,促进肛瘘大鼠模型的术后伤口愈合】。]

L Wang, W Qi, J Gao, M Tian, J Xu
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引用次数: 0

摘要

目的:探讨通滞洗剂(TYX)促进肛瘘术后伤口愈合的机制:方法:利用 TCMSP 和 BATMAN 数据库对通阳效洗剂的有效成分和药物靶点进行研究,利用 GeneCards 和 OMIM 数据库对与伤口愈合相关的靶点进行筛选:方法:利用TCMSP和BATMAN数据库对通畅养生露的有效成分和药物靶点进行研究,利用GeneCards和OMIM数据库筛选与伤口愈合相关的靶点,并利用蛋白质相互作用(PPI)分析、GO和KEGG富集分析对药物和伤口相关靶点进行交叉分析。在 25 只模拟肛瘘手术的 SD 大鼠模型中,与高锰酸钾(PP)溶液相比,评估了低、中、高剂量(每天一次,连续 14 天)TYX 敷料对伤口愈合的影响。用 HE 染色法检查伤口肉芽组织的病理变化,并用免疫组化法检测 TNF-α 的表达。使用 RT-qPCR、Western 印迹或 ELISA 检测肉芽组织中 1β、TNF-α、IL-6 mRNA 和蛋白质的表达:结果:网络药理学分析得出了 156 个 TYX 与伤口愈合之间的共同靶点,其中 IL-1β、TNF- α 和 IL-6 被确定为 TYX 促进伤口愈合的潜在靶点。TYX 的六种核心成分能够与 IL-1β、TNF-α 和 IL-6 结合,结合能均低于 -6.0 Kcal/mol。在大鼠模型中,使用 TYX 和 PP 溶液敷料的伤口明显减少了炎症细胞浸润,增加了成纤维细胞和胶原沉积。三种剂量的 TYX 和 PP 溶液都能明显降低肉芽组织中 IL-6、IL-1β、TNF-α mRNA 和 IL-6 蛋白的表达,但在降低 TNF-α 蛋白表达、TNF-α 和 IL-6 的 mRNA 表达方面,中剂量和高剂量 TYX 的效果明显强于 PP 溶液:结论:TYX 可通过下调炎症因子和减轻伤口炎症来加速伤口愈合。
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[Tongyangxiao Lotion promotes postoperative wound healing in a rat model of anal fistula by downregulating inflammatory factors and suppressing inflammation].

Objective: To explore the mechanism of Tongyangxiao Lotion (TYX) for promoting wound healing following surgery for anal fistula.

Methods: The active ingredients and drug targets of TYX were explored using TCMSP and BATMAN databases, and the targets associated with wound healing were screened using GeneCards and OMIM databases; the intersecting drug and wound-related targets were analyzed with protein-protein interaction (PPI) analysis and GO and KEGG enrichment analyses. In 25 SD rat models with simulated anal fistula surgery, the effect of wound dressing with TYX at low, medium and high doses (once daily for 14 days) on wound healing were assessed in comparison with potassium permanganate (PP) solution. The granulation tissues collected from the wounds were examined for pathological changes with HE staining and for TNF-α expression using immunohistochemistry. The expressions of 1β, TNF-α, IL-6 mRNA and proteins in the granulation tissue were detected using RT-qPCR, Western blotting or ELISA.

Results: Network pharmacology analysis yielded 156 common targets between TYX and wound healing, and among them IL-1β, TNF- α, and IL-6 were identified as potential targets of TYX for promoting wound healing. Six core components of TYX were capable of binding to IL-1β, TNF-α, and IL-6 with binding energies all below -6.0 Kcal/mol. In the rat models, the wounds with TYX and PP solution dressing showed significantly reduced inflammatory cell infiltration and increased fibroblasts and collagen deposition. TYX at the 3 doses and PP solution all significantly reduced the expressions of IL-6, IL-1β, TNF-α mRNA and IL-6 protein in the granulation tissues, but TYX at the medium and high doses produced significantly stronger effects than PP solution for lowering TNF-α protein expression and mRNA expressions of TNF- α and IL-6.

Conclusion: TYX accelerates wound healing by down-regulating the inflammatory factors and reducing inflammation in the wounds.

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