School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, People's Republic of China.
Department of Pharmacy, Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, 610091, People's Republic of China.
Drug Des Devel Ther. 2021 Sep 29;15:4125-4140. doi: 10.2147/DDDT.S328333. eCollection 2021.
Huangtu decoction (HTD) has been widely used in the treatment of gastrointestinal bleeding, ulcerative colitis (UC) and gastrointestinal tumors in China, but its active compounds and mechanism are still not clear yet. The present research aimed to identify the active compounds and mechanism of HTD for the treatment of UC.
Firstly, the chemical compounds of HTD were qualitatively identified based on Q Exactive Orbitrap LC-MS/MS, and their potential targets were predicted through SwissTargetPrediction. Secondly, the differential expressed genes (DEGs) in colon tissues of UC patients and normal controls were retrieved from the GEO database. Thirdly, the overlapping targets of DEGs and the predicted targets were obtained and subjected to GO and KEGG analysis. Finally, the key targets in the most significantly enriched pathway were verified by in vivo experiment, and the protein and mRNA expressions of matrix metalloproteinase-1 (MMP1), MMP3, MMP7, MMP9 and MMP12 were determined by immunohistochemistry (IHC), Western blotting (WB) and quantitative real-time-PCR (qRT-PCR).
A total of 47 compounds were identified and 29 overlapping targets were obtained from HTD extract. The most significantly enriched pathway of overlapping targets involved was MMP. HTD improved the pathological damage in colon tissues of DSS-induced UC model and significantly decreased the serum levels of IL-1β and IL-6. The protein and mRNA expressions of MMP1, MMP3 and MMP9 in colon tissues were significantly decreased after HTD treatment.
HTD treatment can alleviate the colonic inflammation via inhibiting MMPs including MMP1, MMP3 and MMP9.
黄土汤(HTD)在中国被广泛用于治疗胃肠道出血、溃疡性结肠炎(UC)和胃肠道肿瘤,但它的活性化合物和作用机制尚不清楚。本研究旨在确定 HTD 治疗 UC 的活性化合物和作用机制。
首先,基于 Q Exactive Orbitrap LC-MS/MS 对 HTD 的化学化合物进行定性鉴定,并通过 SwissTargetPrediction 预测其潜在靶点。其次,从 GEO 数据库中检索 UC 患者和正常对照者结肠组织中的差异表达基因(DEGs)。然后,获得 DEGs 和预测靶点的重叠靶点,并进行 GO 和 KEGG 分析。最后,通过体内实验验证最显著富集通路中的关键靶点,并通过免疫组织化学(IHC)、Western blot(WB)和定量实时 PCR(qRT-PCR)测定基质金属蛋白酶-1(MMP1)、MMP3、MMP7、MMP9 和 MMP12 的蛋白和 mRNA 表达。
从 HTD 提取物中鉴定出 47 种化合物,并获得 29 个重叠靶点。重叠靶点最显著富集的通路涉及 MMP。HTD 改善了 DSS 诱导的 UC 模型结肠组织的病理损伤,并显著降低了血清中 IL-1β和 IL-6 的水平。HTD 治疗后,结肠组织中 MMP1、MMP3 和 MMP9 的蛋白和 mRNA 表达明显降低。
HTD 治疗可通过抑制 MMP1、MMP3 和 MMP9 等 MMP 缓解结肠炎症。