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黄芪建中汤治疗慢性萎缩性胃炎的物质基础研究:基于尿代谢组学和 SystemsDock 的整合。

Material basis research for Huangqi Jianzhong Tang against chronic atrophic gastritis rats through integration of urinary metabonomics and SystemsDock.

机构信息

Modern Research Center for Traditional Chinese Medicine of Shanxi University, No. 92, Wucheng Road, Taiyuan 030006, Shanxi, PR China; Department of Pharmacy, Shanxi Provincial Hospital of Traditional Chinese Medicine, Taiyuan 030012, PR China.

Modern Research Center for Traditional Chinese Medicine of Shanxi University, No. 92, Wucheng Road, Taiyuan 030006, Shanxi, PR China; College of Chemistry and Chemical Engineering of Shanxi University, No. 92, Wucheng Road, Taiyuan 030006, Shanxi, PR China; Department of Pharmacy, Shanxi Provincial Hospital of Traditional Chinese Medicine, Taiyuan 030012, PR China.

出版信息

J Ethnopharmacol. 2018 Sep 15;223:1-9. doi: 10.1016/j.jep.2018.05.015. Epub 2018 May 17.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Huangqi Jianzhong Tang (HQJZ), a celebrated traditional Chinese medicine (TCM), is commonly used for treatment of chronic atrophic gastritis (CAG) in China.

AIM OF THE STUDY

We aimed to screen out the material basis of HQJZ against CAG.

MATERIALS AND METHODS

CAG rat model was constructed by alternant administrations of ammonia solution and sodium deoxycholate, and the hunger disorder method. Body weight, biochemical indexes and histopathological exam were used to evaluate the efficacy of HQJZ. H NMR-based metabonomics was employed to analyze the urine metabolic features of HQJZ deviated from CAG rats. SystemsDock analysis was utilized to explore the active compounds involved into the efficacy of HQJZ against CAG based on the targeted metabolic biomarkers.

RESULTS

The metabonomic results indicated that HQJZ could significantly improve 16 urinary perturbed metabolites in CAG rats, which were involved into the metabolism of energy and amino acids. And then 28 related proteins and genes were selected out to be the potential targets of HQJZ against CAG based on the six key metabolites closely correlating with biochemical indexes (α-ketoglutarate, valine, sarcosine, glycine, malonate and fumarate). 71 previous identified compounds were docked through systemsDock-aided molecular docking experiments. And the constructed herb-component-protein-metabolite interaction network (HCPMN) revealed the associations between the herbal formulae and CAG. At last, 51 compounds of them were screened as promising active constitutes for the inhibition of CAG, which could act on various targeted proteins.

CONCLUSIONS

he results showed that the approach integrating of metabonomics and systemsDock is a powerful tool to obtain the material basis and regulatory mechanism of TCM formula.

摘要

民族药理学相关性

黄芪建中汤(HQJZ)是一种著名的中药,常用于治疗中国的慢性萎缩性胃炎(CAG)。

研究目的

我们旨在筛选 HQJZ 治疗 CAG 的物质基础。

材料和方法

通过交替给予氨溶液和脱氧胆酸钠以及饥饿障碍法构建 CAG 大鼠模型。体重、生化指标和组织病理学检查用于评估 HQJZ 的疗效。基于 H NMR 的代谢组学用于分析 HQJZ 偏离 CAG 大鼠的尿液代谢特征。系统对接分析用于基于靶向代谢生物标志物探索 HQJZ 治疗 CAG 的活性化合物。

结果

代谢组学结果表明,HQJZ 可显著改善 CAG 大鼠的 16 种尿液扰动代谢物,这些代谢物涉及能量和氨基酸代谢。然后,基于与生化指标密切相关的六个关键代谢物(α-酮戊二酸、缬氨酸、肌氨酸、甘氨酸、丙二酸和富马酸),选择了 28 个相关蛋白和基因作为 HQJZ 治疗 CAG 的潜在靶点。通过系统对接辅助分子对接实验对 71 种先前鉴定的化合物进行了对接。构建的草药成分-蛋白质-代谢物相互作用网络(HCPMN)揭示了草药配方与 CAG 之间的关联。最后,筛选出其中的 51 种化合物作为抑制 CAG 的潜在活性成分,这些成分可作用于多种靶向蛋白。

结论

结果表明,代谢组学和系统对接相结合的方法是获得中药配方物质基础和调节机制的有力工具。

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