[黄连与杜仲通过能量代谢对溃疡性结肠炎的协同作用]。

Q3 Pharmacology, Toxicology and Pharmaceutics
Chuan-Wei Qiu, Yi Zhang, Zhen-Ye Luo, Feng-Lin Zhang, Ting Xia, Fei-Long Chen, Xiao-Mei Tan, Chang-Shun Liu
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引用次数: 0

摘要

给小鼠注射4%葡聚糖硫酸钠诱导UC模型,然后随机分为模型组、CR组和ECR组。治疗14天后,通过结肠组织病理学和炎症指标评估处理对UC的治疗效果。进行了靶向能量代谢组学分析,以评估加工对结肠组织能量代谢的影响。通过分子对接预测了能量代谢物与肠道屏障紧密连接蛋白Claudin和葡萄糖转运体2(GLUT2)的结合亲和力。在大鼠体内进行了单向肠灌流实验,以评估加工对肠道葡萄糖转运的影响。结果表明,CR和ECR均能修复UC小鼠结肠组织损伤,下调组织炎症因子白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)水平,其中ECR的疗效优于CR。加工产品能明显上调结肠组织糖酵解、三羧酸循环和氧化磷酸化过程中多种代谢物的水平,其中上调的1,6-二磷酸果糖和乙酰辅酶A能与Claudin和GLUT2很好地结合。此外,加工产物还能增加 GLUT2 的表达,增强葡萄糖转运活性。这项研究表明,ECR 可增强葡萄糖转运,从而改善结肠能量代谢,促进屏障修复,并通过加工发挥协同作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Synergistic effect of Coptidis Rhizoma processed with Euodiae Fructus on ulcerative colitis through energy metabolism].

Based on the differences in targeted energy metabolomics, intestinal barrier protein expression, and glucose transport,the synergistic mechanism of Coptidis Rhizoma(CR) processed with Euodiae Fructus(ECR) on ulcerative colitis(UC) was explored.Mice were administered 4% dextran sulfate sodium to induce UC model, and then randomly divided into a model group, a CR group,and an ECR group. After 14 days of treatment, the therapeutic effect of processing on UC was assessed through histopathology of colon tissue and inflammatory indexes. Targeted energy metabolomics analysis was performed to evaluate the effect of processing on colon tissue energy metabolism. Molecular docking was carried out to predict the binding affinity of energy metabolites with intestinal barrier tight junction protein Claudin and glucose transporter 2(GLUT2). In vivo unidirectional intestinal perfusion experiments in rats were conducted to evaluate the effect of processing on intestinal glucose transport. The results showed that both CR and ECR could repair colon tissue damage in UC mice, downregulate tissue inflammatory factors interleukin-6(IL-6) and tumor necrosis factor-α(TNF-α)levels, with the efficacy of ECR being superior to CR. Processed products significantly upregulated levels of multiple metabolites in colon tissue glycolysis, tricarboxylic acid cycle, and oxidative phosphorylation, among which the upregulated levels of 1,6-diphosphate fructose and acetyl coenzyme A could bind well with Claudin and GLUT2. Additionally, the processed product also increased the expression of GLUT2 and enhanced glucose transport activity. This study suggests that ECR may enhance glucose transport to improve colon energy metabolism, promote barrier repair, and exert synergistic effects through processing.

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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