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采用超高效液相色谱-高分辨率质谱联用结合模式识别方法和代谢途径分析研究番荔枝的毒性。

Metabolomics study on the toxicity of Annona squamosa by ultraperformance liquid-chromatography high-definition mass spectrometry coupled with pattern recognition approach and metabolic pathways analysis.

机构信息

Nanjing University of Chinese Medicine, Pharmaceutical institute, Nanjing 210046, China.

出版信息

J Ethnopharmacol. 2016 May 26;184:187-95. doi: 10.1016/j.jep.2016.03.006. Epub 2016 Mar 7.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Annona squamosa Linn (Annonaceae) is a commonly used and effective traditional Chinese medicine (TCM) especially in the South China. The seeds of Annona squamosa Linn (SAS) have been used as a folk remedy to treat "malignant sores" (cancer) in South of China, but they also have high toxicity on human body.

AIM OF THE STUDY

To discover the potential biomarkers in the mice caused by SAS.

MATERIALS AND METHODS

We made metabonomics studies on the toxicity of SAS by ultraperformance liquid-chromatography high-definition mass spectrometry coupled with pattern recognition approach and metabolic pathways analysis.

RESULTS

The significant difference in metabolic profiles and changes of metabolite biomarkers between the Control group and SAS group were well observed. 11 positive ions and 9 negative ions (P<0.05) were indicated based on UFLC-QTOF-HDMS. The metabolic pathways of SAS group are discussed according to the identified endogenous metabolites, and eight metabolic pathways are identified using Kyoto Encyclopedia of Genes and Genomes (KEGG).

CONCLUSIONS

The present study demonstrates that metabonomics analysis could greatly facilitate and provide useful information for the further comprehensive understanding of the pharmacological activity and potential toxicity of SAS in the progress of them being designed to a new anti-tumor medicine.

摘要

民族药理学相关性

番荔枝(番荔枝科)是一种常用且有效的中药,特别是在中国南方。番荔枝的种子(SAS)已被用作民间疗法来治疗中国南方的“恶性溃疡”(癌症),但它们对人体也有很高的毒性。

研究目的

发现 SAS 引起的小鼠潜在生物标志物。

材料和方法

我们通过超高效液相色谱-高清晰度质谱联用模式识别方法和代谢途径分析对 SAS 的毒性进行代谢组学研究。

结果

在对照组和 SAS 组之间,代谢谱和代谢物生物标志物的变化有明显差异。基于 UFLC-QTOF-HDMS,鉴定出 11 个正离子和 9 个负离子(P<0.05)。根据鉴定出的内源性代谢物,对 SAS 组的代谢途径进行了讨论,并利用京都基因与基因组百科全书(KEGG)鉴定了 8 条代谢途径。

结论

本研究表明,代谢组学分析可以极大地促进和提供有用的信息,有助于进一步全面了解 SAS 的药理活性和潜在毒性,以设计出一种新的抗肿瘤药物。

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