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左金丸治疗慢性非萎缩性胃炎患者的代谢组学特征

Metabolomics Profiles Associated with the Treatment of Zuojin Pill on Patients with Chronic Nonatrophic Gastritis.

作者信息

Ma Xiao, Xie Shuying, Wang Ruilin, Wang Zhongxia, Jing Manyi, Li Haotian, Wei Shizhang, Liu Honghong, Li Jianyu, He Qingyong, Zhao Yanling

机构信息

Department of Pharmacy, Chinese PLA General Hospital, Beijing, China.

School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Front Pharmacol. 2022 Jul 11;13:898680. doi: 10.3389/fphar.2022.898680. eCollection 2022.

DOI:10.3389/fphar.2022.898680
PMID:35899115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9310101/
Abstract

Chronic nonatrophic gastritis (CNG) is the most common digestive disease. In China, Zuojin pill (ZJP) is considered an effective medicine formula for CNG. However, its efficacy and mechanism have never been explored. In order to understand how and why ZJP demonstrates therapeutic effect on CNG, a clinical trial was conducted. Metabolomics was used to explore its deep mechanism. A total of 14 patients with CNG were recruited from October 2020 to March 2021 (ChiCTR2000040549). The endoscopy and histopathological changes were evaluated as efficacy. Serum samples were prepared and detected by performing widely targeted metabolome using UPLC. Multivariate statistical analysis was conducted to identify potential differential metabolites and signaling pathways. Last, the signal-related inflammatory factors containing COX-2, IL-4, and IL-17 were confirmed via immunohistochemical staining and enzyme-linked immunosorbent assay. ZJP was able to alleviate several indexes of mucosal injury under endoscopy and histology. Erosion and bile reflux, but not red plaques and hemorrhage, were downregulated by ZJP. In addition, it could remarkably alleviate active chronic inflammation. A total of 14 potential metabolites, namely, hypoxanthine, adipic acid, D-ribono-1,4-lactone, L-sepiapterin, imidazoleacetic acid, sebacate, ADP-ribose, 4-hydroxybenzyl alcohol, 11,12-EET, 15-OxoETE, 12-OxoETE, (±)8-HETE, glycyrrhizinate, and DL-aminopimelic acid, were discriminated by metabolomics. Moreover, certain amino acid metabolism got significance during the disease progress and treatment. The related inflammatory factors including COX-2, IL-4, and IL-17 were inhibited by ZJP in both mucosa and serum. All these results indicated that ZJP partially acts as an inflammatory suppressor to regulate comprehensive metabolism disorders. This might be an important mechanism of ZJP in the treatment of CNG.

摘要

慢性非萎缩性胃炎(CNG)是最常见的消化系统疾病。在中国,左金丸(ZJP)被认为是治疗CNG的有效方剂。然而,其疗效和作用机制尚未得到探索。为了了解ZJP对CNG的治疗方式及原因,开展了一项临床试验。采用代谢组学方法探究其深层机制。2020年10月至2021年3月共招募了14例CNG患者(ChiCTR2000040549)。以内镜检查和组织病理学变化评估疗效。制备血清样本,采用超高效液相色谱法进行广泛靶向代谢组检测。进行多变量统计分析以识别潜在的差异代谢物和信号通路。最后,通过免疫组织化学染色和酶联免疫吸附测定法确认含COX-2、IL-4和IL-17的信号相关炎症因子。ZJP能够改善内镜检查和组织学下的多项黏膜损伤指标。ZJP可下调糜烂和胆汁反流,但对红斑和出血无影响。此外,它能显著减轻活动性慢性炎症。代谢组学鉴别出14种潜在代谢物,即次黄嘌呤、己二酸、D-核糖-1,4-内酯、L-蝶酰三谷氨酸、咪唑乙酸、癸二酸、ADP-核糖、4-羟基苄醇、11,12-EET、15-氧代ETE、12-氧代ETE、(±)8-HETE、甘草酸盐和DL-氨基庚二酸。此外,某些氨基酸代谢在疾病进展和治疗过程中具有重要意义。ZJP在黏膜和血清中均抑制了包括COX-2、IL-4和IL-17在内的相关炎症因子。所有这些结果表明,ZJP部分作为炎症抑制剂发挥作用,调节综合代谢紊乱。这可能是ZJP治疗CNG的重要机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f8c/9310101/4eec77635d3b/fphar-13-898680-g007.jpg
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