Chenyang Fang, Yanni Pei, Yunhua Peng, Hong Lu, Yin Qu, Chunsheng Luo, Yafeng Lu, Wei Yang
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引用次数: 0
摘要
克罗恩病(CD)是一种病因不明的消化系统慢性炎症性疾病,其发病率在世界范围内呈上升趋势。然而,目前没有有效的治疗方法或药物可用于个体乳糜泻。因此,迫切需要新的治疗策略。利用The Traditional Chinese Systems Pharmacology数据库对清化消瘀方(QHXYF)化合物相关的生物活性化合物和靶点进行检测,并利用5个疾病靶点数据库对cd相关疾病靶点进行鉴定。从qhxyf相关和cd相关疾病靶点中共鉴定出166个重叠靶点,发现它们在氧化应激相关通路和PI3K/AKT信号通路中富集。然后使用分子对接来预测生物活性化合物如何与中心靶点结合。发现槲皮素可能是核心生物活性化合物,与前5个枢纽靶点具有良好的结合亲和力。最后,通过动物实验进一步验证上述发现,结果显示QHXYF或槲皮素通过抑制PI3K/AKT通路抑制2,4,6-三硝基苯磺酸诱导的炎症和氧化应激过程,从而改善CD症状。这些发现表明QHXYF和槲皮素可能是治疗CD的潜在新方法。
Network pharmacology and molecular docking reveal the mechanism of Qinghua Xiaoyong Formula in Crohn's disease.
Crohn's disease (CD) is a chronic inflammatory illness of the digestive system with unknown etiology, and its incidence is increasing worldwide. However, there are currently no effective treatments or medications available for individuals with CD. Therefore, novel therapeutic strategies are urgently needed. The bioactive compounds and targets associated with compounds of Qinghua Xiaoyong Formula (QHXYF) were examined using The Traditional Chinese Medicine Systems Pharmacology database, and 5 disease target databases were also used to identify CD-related disease targets. A total of 166 overlapping targets were identified from QHXYF-related and CD-related disease targets and they were found to be enriched in oxidative stress-related pathways and the PI3K/AKT signaling pathway. Molecular docking was then used to predict how the bioactive compounds would bind to the hub targets. It was found that quercetin could be the core bioactive compound and had good binding affinity to the top 5 hub targets. Finally, animal experiments were performed to further validate the findings, and the results revealed that QHXYF or quercetin inhibited 2,4,6-trinitrobenzenesulfonic acid-induced inflammation and oxidative stress processes by inhibiting the PI3K/AKT pathway, thereby improving CD symptoms. These findings suggest that QHXYF and quercetin may be potential novel treatments for CD.
期刊介绍:
The Korean Journal of Physiology & Pharmacology (Korean J. Physiol. Pharmacol., KJPP) is the official journal of both the Korean Physiological Society (KPS) and the Korean Society of Pharmacology (KSP). The journal launched in 1997 and is published bi-monthly in English. KJPP publishes original, peer-reviewed, scientific research-based articles that report successful advances in physiology and pharmacology. KJPP welcomes the submission of all original research articles in the field of physiology and pharmacology, especially the new and innovative findings. The scope of researches includes the action mechanism, pharmacological effect, utilization, and interaction of chemicals with biological system as well as the development of new drug targets. Theoretical articles that use computational models for further understanding of the physiological or pharmacological processes are also welcomed. Investigative translational research articles on human disease with an emphasis on physiology or pharmacology are also invited. KJPP does not publish work on the actions of crude biological extracts of either unknown chemical composition (e.g. unpurified and unvalidated) or unknown concentration. Reviews are normally commissioned, but consideration will be given to unsolicited contributions. All papers accepted for publication in KJPP will appear simultaneously in the printed Journal and online.