Evidence map›Paper›PMID 28445133›Full record

ArticleOncotarget2017

Baicalein decreases uric acid and prevents hyperuricemic nephropathy in mice.

Xiaolu Meng, Zhuo Mao, Xin Li, Dandan Zhong, Min Li, Yingli Jia, Jing Wei, Baoxue Yang, Hong Zhou

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Biomolecules · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Mechanism ofDrug design, development and therapy · 2025
    Article
  10. Article
  11. The potential of Chinese medicines in the treatment of hyperuricemia.American journal of translational research · 2023
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Xiaolu MengDepartment of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, 100191, P.R. China.
Zhuo MaoTianjin Key Laboratory for Modern Drug Delivery and High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, 300072, P.R. China.
Xin LiDrug Clinical Trial Institution, The Affiliated Hospital of Qingdao University, Qingdao, 266003, P.R. China.
Dandan ZhongDepartment of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, 100191, P.R. China.
Min LiDepartment of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, 100191, P.R. China.
Yingli JiaDepartment of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, 100191, P.R. China.
Jing WeiTianjin Key Laboratory for Modern Drug Delivery and High-Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, 300072, P.R. China.
Baoxue YangDepartment of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, 100191, P.R. China.
Hong ZhouDepartment of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing, 100191, P.R. China.
Peking University · CNTianjin University · CNAffiliated Hospital of Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Baicalein, a natural flavonoid, is structurally advantageous for binding to xanthine oxidoreductase. In our study, molecular docking analysis and Surface Plasmon Resonance revealed a direct interaction between baicalein and xanthine oxidoreductase. Moreover, 50 mg/kg/d baicalein treatment significantly suppressed the viability of xanthine oxidoreductase in hyperuricemia mouse model. The data showed that baicalein remarkably prevented renal dysfunction, ameliorated kidney fibrosis, alleviated epithelial-mesenchymal transition and oxidative stress in hyperuricemia mice. Thus, we concluded that baicalein executed a kidney-protection action in hyperuricemia and therefore may be used as a therapeutic alternative for hyperuricemic nephropathy.

Indexed as

AnimalsAntioxidantsDisease Models, AnimalEpithelial-Mesenchymal TransitionFlavanonesGoutHyperuricemiaKidneyKidney DiseasesMaleMiceMice, Inbred ICRMolecular Docking SimulationOxidative StressSurface Plasmon ResonanceXanthine DehydrogenaseAntioxidantsbaicaleinFlavanonesXanthine Dehydrogenasebaicaleinhyperuricemianephropathyuric acidxanthine oxidoreductase

Identifiers

PMID28445133
PMCPMC5522264
OpenAlexW2604214173

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.