Kaempferol Suppresses Mesothelial–Mesenchymal Transition and Attenuates Postoperative Peritoneal Adhesions by Blocking the TNF-α/COX2 Signalling Pathway

IF 2.5 4区 医学 Q2 Medicine
Li Zhang, Gan Li, Yiwei Ren, Yanjun Sun, Kai Deng, Lindi Cai, Enmeng Li, Tianli Shen, Xuqi Li, Cancan Zhou
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引用次数: 0

Abstract

Postoperative peritoneal adhesion (PA) formation is a common complication after abdominal surgery and can result in various severe outcomes. Inflammation and fibrosis are important processes in PA formation. The effectiveness of kaempferol (KF), a common component of several medications used to reduce inflammation and prevent fibrotic diseases, in preventing postoperative PA formation is unknown. This study explored the effectiveness and mechanism of KF in preventing PA formation following surgery. The animal adhesion model revealed that KF could effectively prevent adhesions formation and inhibit mesothelial–mesenchymal transition (MMT). Protein–protein interaction and pathway enrichment analyses revealed that TNF-α may be the key target through which KF prevents adhesion formation. Here, KF was found to inhibit TNF-α-induced MMT. Furthermore, Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses revealed that common genes between KF and PA are enriched in the TNF signalling pathway. Moreover, cyclooxygenase 2 (COX2) was identified as a downstream target of TNF-α whose expression is positively correlated with adhesion formation. Most importantly, COX2 small interfering RNA (siRNA) and overexpression plasmid (OE) transfection experiments confirmed that KF inhibits MMT by blocking the TNF-α/COX2 signalling pathway. Finally, molecular docking revealed that TNF-α is a binding target of KF. In conclusion, these results suggest that KF inhibits MMT by blocking the TNF-α/COX2 signalling pathway, thus attenuating adhesion formation. These results provide new insights into the development of antiadhesion drugs.

山奈酚通过阻断TNF-α/COX2信号通路抑制术后腹膜粘连
术后腹膜粘连(PA)形成是腹部手术后常见的并发症,可导致各种严重后果。炎症和纤维化是PA形成的重要过程。山奈酚(KF)是几种用于减少炎症和预防纤维化疾病的药物的常见成分,其在预防术后PA形成方面的有效性尚不清楚。本研究探讨KF预防术后PA形成的有效性和机制。动物黏附模型显示,KF能有效阻止黏附形成,抑制间充质转化(MMT)。蛋白-蛋白相互作用和途径富集分析显示TNF-α可能是KF阻止粘附形成的关键靶点。本研究发现KF可抑制TNF-α-诱导的MMT。此外,京都基因和基因组百科全书通路富集分析显示,KF和PA之间的共同基因在TNF信号通路中富集。此外,环氧化酶2 (COX2)被鉴定为TNF-α的下游靶标,其表达与粘附形成呈正相关。最重要的是,COX2小干扰RNA (siRNA)和过表达质粒(OE)转染实验证实,KF通过阻断TNF-α/COX2信号通路抑制MMT。最后,分子对接发现TNF-α是KF的结合靶点。综上所述,这些结果表明KF通过阻断TNF-α/COX2信号通路抑制MMT,从而减弱粘连形成。这些结果为抗粘连药物的开发提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
128
审稿时长
6 months
期刊介绍: Clinical and Experimental Pharmacology and Physiology is an international journal founded in 1974 by Mike Rand, Austin Doyle, John Coghlan and Paul Korner. Our focus is new frontiers in physiology and pharmacology, emphasizing the translation of basic research to clinical practice. We publish original articles, invited reviews and our exciting, cutting-edge Frontiers-in-Research series’.
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