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从[植物名称未给出]中进行生物活性导向的潜在抗腹泻成分分离及分子对接评估。

Bioactivity-guided isolation of potential antidiarrheal constituents from L. and molecular docking evaluation.

作者信息

Wu Junkai, Zhang Xiaomeng, Guo Liyang, Sheng Zunlai

机构信息

School of Pharmacy, Quanzhou Medical College, Quanzhou, China.

College of Veterinary Medicine, Northeast Agricultural University, Harbin, China.

出版信息

Front Vet Sci. 2024 Aug 29;11:1451615. doi: 10.3389/fvets.2024.1451615. eCollection 2024.

DOI:10.3389/fvets.2024.1451615
PMID:39268517
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11390441/
Abstract

BACKGROUND

L., a member of the Euphorbiaceae family, is extensively used as a folk medicine across various regions. In China, its decoction is traditionally consumed to alleviate diarrhea. This study aimed to evaluate the antidiarrheal activities of and to identify its bioactive constituents through a bioactivity-guided isolation technique.

METHODS

Oral administration of extract to mice was conducted to assess its effects on diarrhea. The anti-diarrheal effects were investigated in an aqueous extract and in three fractions of varying polarities derived from the aqueous extract, as well as in different eluates from D-101 macroporous resin, and in the compounds quercitrin and isoquercitrin, using mouse models with castor oil-induced diarrhea.

RESULTS

The aqueous extract demonstrated significant anti-diarrheal activities in a dose-dependent manner in the castor oil-induced diarrheal model. Notably, the ethyl acetate (EtOAc) fraction showed prominent effects. Through bioactivity-guided isolation, two major compounds, isoquercitrin and quercitrin from the active fraction were found to possess antidiarrheal effects. Molecular docking studies revealed that the affinity energy of isoquercitrin and quercitrin were -8.5 and -8.2 kcal mol, respectively, which were comparable to the reference drug loperamide, with an affinity energy of -9.1 kcal mol.

CONCLUSION

This research provides evidence supporting the development of as a therapeutic agent for diarrhea, with isoquercitrin and quercitrin emerging as two key constituents that are likely responsible for its antidiarrheal activity. These findings validate the traditional use of and highlight its potential as a natural treatment for diarrhea.

摘要

背景

大戟科植物[植物名称未给出,用L.代替]在各个地区被广泛用作民间药物。在中国,传统上饮用其煎剂来缓解腹泻。本研究旨在评估[植物名称未给出,用L.代替]的止泻活性,并通过生物活性导向分离技术鉴定其生物活性成分。

方法

对小鼠口服[植物名称未给出,用L.代替]提取物,以评估其对腹泻的影响。使用蓖麻油诱导腹泻的小鼠模型,研究了水提取物、水提取物衍生的三种不同极性的馏分、D - 101大孔树脂的不同洗脱液以及化合物槲皮苷和异槲皮苷的止泻作用。

结果

在蓖麻油诱导的腹泻模型中,水提取物呈剂量依赖性地表现出显著的止泻活性。值得注意的是,乙酸乙酯(EtOAc)馏分显示出突出的效果。通过生物活性导向分离,发现活性馏分中的两种主要化合物异槲皮苷和槲皮苷具有止泻作用。分子对接研究表明,异槲皮苷和槲皮苷的亲和能分别为 - 8.5和 - 8.2 kcal·mol,与参考药物洛哌丁胺的亲和能 - 9.1 kcal·mol相当。

结论

本研究为将[植物名称未给出,用L.代替]开发为腹泻治疗药物提供了证据,异槲皮苷和槲皮苷是其可能具有止泻活性的两个关键成分。这些发现验证了[植物名称未给出,用L.代替]的传统用途,并突出了其作为腹泻天然治疗方法潜在价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26c2/11390441/faf3e037c698/fvets-11-1451615-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26c2/11390441/a649a23e7f6c/fvets-11-1451615-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26c2/11390441/dc0dea77d625/fvets-11-1451615-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26c2/11390441/faf3e037c698/fvets-11-1451615-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26c2/11390441/a649a23e7f6c/fvets-11-1451615-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26c2/11390441/dc0dea77d625/fvets-11-1451615-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26c2/11390441/faf3e037c698/fvets-11-1451615-g003.jpg

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