Shi Jia-Xin, Huo Jin-Nan, Luo Xi, Zhang Qiang, Han Li-Ying, Wu Xi, Bao Yong-Rui, Wang Shuai, Li Tian-Jiao, Dong Bao-Qiang, Meng Xian-Sheng
College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, Liaoning Province, 116600, China.
College of Acupuncture-Moxibustion and Tuina, Liaoning University of Traditional Chinese Medicine, Shenyang, Liaoning Province, 110847, China.
J Ethnopharmacol. 2025 May 12;347:119730. doi: 10.1016/j.jep.2025.119730. Epub 2025 Apr 4.
Gastric ulcer (GU) is a common multifactorial gastrointestinal disorder, affecting millions of people worldwide. Mu Jin Powder (MJP), a renowned herbal pair, was recorded in Yizong Jinjian by Wu Qian during the Qing dynasty. This combination has been integrated into traditional Chinese medicine (TCM) prescriptions for gastrointestinal diseases, particularly GU, and has demonstrated significant results in modern medicine studies. However, the specific advantages of MJP for GU and its underlying mechanisms remain insufficiently understood, requiring further investigation.
To assess the preventive effects of MJP on ethanol-induced gastric mucosal injury and elucidate its underlying mechanisms.
This study was based on ethanol induced SD rat model to elucidate the pharmacological effects of MJP. The chemical components of MJP and the absorbed components in the serum of treated rats were identified by UPLC-Q-TOF-MS. Serum metabolomics and Network pharmacology were applied to investigate the potential mechanisms of MJP against GU, and the mechanistic pathways were verified through PCR and Western blot analyses.
In vivo pharmacological experiments demonstrated that MJP significantly reduced ulcer area and improved the histopathological features of gastric tissues. Fifty-three chemical components were determined in MJP, and 18 absorbed components were detected in the serum of treated rats for the first time. Non-targeted serum metabolomics revealed 28 significantly altered differential metabolites, most of which were modulated and normalized by MJP. Comprehensive network pharmacology and metabolomics analyses indicated that MJP exerted anti-GU effects by intervening in 5 key target proteins (PTG2, CHRNA7, CA1, PTG1, CASP3, and AKT1) and regulating differential metabolites. PCR and Western blot analyses suggested that MJP may inhibit the PI3K/Akt/NF-κB pathway to prevent ethanol-induced gastric ulcers.
Mu Jin Powder effectively ameliorates ethanol-induced gastric ulcers in rats, potentially by inhibiting the PI3K/Akt/NF-κB pathway.
胃溃疡(GU)是一种常见的多因素胃肠道疾病,影响着全球数百万人。木金散(MJP)是一种著名的药对,由清代吴谦的《医宗金鉴》记载。这种组合已被纳入治疗胃肠道疾病,特别是胃溃疡的中药方剂中,并在现代医学研究中显示出显著效果。然而,木金散对胃溃疡的具体优势及其潜在机制仍了解不足,需要进一步研究。
评估木金散对乙醇诱导的胃黏膜损伤的预防作用,并阐明其潜在机制。
本研究基于乙醇诱导的SD大鼠模型来阐明木金散的药理作用。通过超高效液相色谱-四极杆飞行时间质谱联用仪(UPLC-Q-TOF-MS)鉴定木金散的化学成分以及给药大鼠血清中的吸收成分。应用血清代谢组学和网络药理学研究木金散抗胃溃疡的潜在机制,并通过聚合酶链反应(PCR)和蛋白质免疫印迹法(Western blot)分析验证作用机制途径。
体内药理学实验表明,木金散显著减小溃疡面积,改善胃组织的组织病理学特征。在木金散中确定了53种化学成分,首次在给药大鼠血清中检测到18种吸收成分。非靶向血清代谢组学揭示了28种显著改变的差异代谢物,其中大多数被木金散调节并恢复正常。综合网络药理学和代谢组学分析表明,木金散通过干预5种关键靶蛋白(PTG2、CHRNA7、CA1、PTG1、CASP3和AKT1)并调节差异代谢物发挥抗胃溃疡作用。PCR和Western blot分析表明,木金散可能通过抑制PI3K/Akt/NF-κB途径预防乙醇诱导的胃溃疡。
木金散可有效改善大鼠乙醇诱导的胃溃疡,可能是通过抑制PI3K/Akt/NF-κB途径实现的。