Evidence map›Paper›PMID 28446747›Full record

ArticleScientific reports2017

A Systems Pharmacology Approach to Determine Active Compounds and Action Mechanisms of Xipayi KuiJie'an enema for Treatment of Ulcerative colitis.

Wei Yu, Zhihong Li, Fei Long, Wen Chen, Yurong Geng, Zhiyong Xie, Meicun Yao, Bo Han, Teigang Liu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  3. Network pharmacology andAnnals of medicine · 2022
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  4. Ethanolic Extract fromMolecules (Basel, Switzerland) · 2022
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  10. Article
  11. Review
  12. Article
  13. Article
  14. Frontiers in pharmacology · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Wei YuSchool of Pharmacy, Xinjiang Shihezi University, Xinjiang, 832002, China.
Zhihong LiKey Laboratory of Chinese Internal Medicine of Education, DongZhiMen Hospital, Beijing, 100070, China.
Fei LongSchool of Pharmacy, Xinjiang Shihezi University, Xinjiang, 832002, China.
Wen ChenSchool of Pharmacy, Xinjiang Shihezi University, Xinjiang, 832002, China.
Yurong GengSchool of Pharmacy, Xinjiang Shihezi University, Xinjiang, 832002, China.
Zhiyong XieThe first affiliated hospital, School of medicine, Shihezi university, Xinjiang, 832002, China.
Meicun YaoCollege of pharmacy, Sun yat-sen university, Guangzhou, 510006, China.
Bo HanSchool of Pharmacy, Xinjiang Shihezi University, Xinjiang, 832002, China. 524683221@qq.com.
Teigang LiuCollege of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 100029, China. liutiegang2009@163.com.
Shihezi University · CNBeijing University of Chinese Medicine · CNDongzhimen Hospital Affiliated to Beijing University of Chinese Medicine · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Xipayi Kui Jie'an (KJA), a type of traditional Uygur medicine (TUM), has shown promising therapeutic effects in Ulcerative colitis (UC). Owing to the complexity of TUM, the pharmacological mechanism of KJA remains vague. Therefore, the identification of complex molecular mechanisms is a major challenge and a new method is urgently needed to address this problem. In this study, we established a feasible pharmacological model based on systems pharmacology to identify potential compounds and targets. We also applied compound-target and target-diseases network analysis to evaluate the action mechanisms. According to the predicted results, 12 active compounds were selected and these compounds were also identified by HPLC-ESI-MS/MS analysis. The main components were tannins, this result is consistent with the prediction. The active compounds interacted with 22 targets. Two targets including PTGS2 and PPARG were demonstrated to be the main targets associated with UC. Systematic analysis of the constructed networks revealed that these targets were mainly involved in NF-κB signaling pathway. Furthermore, KJA could also regulate the CD4 + CD25 + Foxp3 + Treg cells. In conclusion, this systems pharmacology-based approach not only explained that KJA could alleviate the UC by regulating its candidate targets, but also gave new insights into the potential novel therapeutic strategies for UC.

Indexed as

EnemaAnimalsChromatography, High Pressure LiquidColitis, UlcerativeImmunologic FactorsMaleMicePlant ExtractsQuercusSpectrometry, Mass, Electrospray IonizationSystems BiologyTandem Mass SpectrometryTanninsImmunologic FactorsPlant ExtractsTannins

Identifiers

PMID28446747
PMCPMC5430631
OpenAlexW2606651701

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.