Yan Jing, Tang Yan, Yu Wei, Jiang Lu, Liu Chen, Li Qi, Zhang Zhiqiang, Shao Changlei, Zheng Yang, Liu Xihao, Liu Xincheng
Department of Physiology, Jining Medical University, Jining City, Shandong Province, China.
Evid Based Complement Alternat Med. 2022 Aug 31;2022:9110704. doi: 10.1155/2022/9110704. eCollection 2022.
Inflammatory bowel disease (IBD) is a major cause of morbidity and mortality due to its repetitive remission and relapse. The Jian-Wei-Yu-Yang (JW) formula has a historical application in the clinic to combat gastrointestinal disorders. The investigation aimed to explore the molecular and cellular mechanisms of JW.
2% dextran sodium sulfate (DSS) was diluted in drinking water and given to mice for 5 days to establish murine models of experimental colitis, and different doses of JW solution were administered for 14 days. Network pharmacology analysis and weighted gene co-expression network analysis (WGCNA) were utilized to predict the therapeutic role of JW against experimental colitis and colitis-associated colorectal cancer (CAC). 16S rRNA sequencing and untargeted metabolomics were conducted using murine feces. Western blotting, immunocytochemistry, and wound healing experiments were performed to confirm the molecular mechanisms.
(1) Liquid chromatography with mass spectrometry was utilized to confirm the validity of the JW formula. The high dose of JW treatment markedly attenuated DSS-induced experimental colitis progression, and the targets were enriched in inflammation, infection, and tumorigenesis. (2) The JW targets were related to the survival probability in patients with colorectal cancer, underlying a potential therapeutic value in CRC intervention. (3) Moreover, the JW therapy successfully rescued the decreased richness and diversity of microbiota, suppressed the potentially pathogenic phenotype of the gut microorganisms, and increased cytochrome P450 activity in murine colitis models. (4) Our experiments confirmed that the JW treatment suppressed caspase3-dependent pyroptosis, hypoxia-inducible factor 1 (HIF1), and interleukin-1b (IL-1b) in the colon; facilitated the alternative activation of macrophages (Ms); and inhibited tumor necrosis factor- (TNF)-induced reactive oxygen species (ROS) level in intestinal organoids (IOs).
The JW capsule attenuated the progression of murine colitis by a prompt resolution of inflammation and bloody stool and by re-establishing a microbiome profile that favors re-epithelization and prevents carcinogenesis.
炎症性肠病(IBD)因其反复缓解和复发,是发病和死亡的主要原因。健脾胃阳(JW)配方在临床上有治疗胃肠道疾病的历史应用。本研究旨在探索JW的分子和细胞机制。
将2%的葡聚糖硫酸钠(DSS)稀释于饮用水中,给予小鼠5天以建立实验性结肠炎小鼠模型,并给予不同剂量的JW溶液14天。利用网络药理学分析和加权基因共表达网络分析(WGCNA)预测JW对实验性结肠炎和结肠炎相关结直肠癌(CAC)的治疗作用。使用小鼠粪便进行16S rRNA测序和非靶向代谢组学分析。进行蛋白质免疫印迹、免疫细胞化学和伤口愈合实验以确认分子机制。
(1)采用液相色谱-质谱联用技术确认JW配方的有效性。高剂量JW治疗显著减轻DSS诱导的实验性结肠炎进展,其靶点富集于炎症、感染和肿瘤发生。(2)JW靶点与结直肠癌患者的生存概率相关,提示其在CRC干预中具有潜在治疗价值。(3)此外,JW疗法成功挽救了小鼠结肠炎模型中微生物群丰富度和多样性的降低,抑制了肠道微生物的潜在致病表型,并增加了细胞色素P450活性。(4)我们的实验证实,JW治疗可抑制结肠中caspase3依赖性细胞焦亡、缺氧诱导因子1(HIF1)和白细胞介素-1β(IL-1β);促进巨噬细胞(Ms)的替代激活;并抑制肿瘤坏死因子-(TNF)诱导的肠道类器官(IOs)中的活性氧(ROS)水平。
JW胶囊通过迅速消除炎症和血便,以及重新建立有利于再上皮化和预防癌变的微生物群谱,减轻了小鼠结肠炎的进展。