Evidence map›Paper›PMID 40432894›Full record

ArticleFrontiers in pharmacology2025

The flavonoid of

Lin Liu, Wen He, Sijing Liu, Yang Li, Peng Wang, Fang Yan, Wenjing Yang, Yongxue Yang, Jinlin Guo

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Overexpression ofaBIOTECH · 2026
    Article
  2. 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.

Lin Liu *College of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Wen He *College of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Sijing Liu *College of Medical Technology, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Yang LiCollege of Public Health, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Peng WangGeriatric Diseases Institute of Chengdu/Cancer Prevention and Treatment Institute of Chengdu, Department of Clinical Trial Center, Chengdu Fifth People's Hospital (The Second Clinical Medical College, Affiliated Fifth People's Hospital of Chengdu University of Traditional Chinese Medicine), Chengdu, China.
Fang YanGeriatric Diseases Institute of Chengdu/Cancer Prevention and Treatment Institute of Chengdu, Department of Clinical Trial Center, Chengdu Fifth People's Hospital (The Second Clinical Medical College, Affiliated Fifth People's Hospital of Chengdu University of Traditional Chinese Medicine), Chengdu, China.
Wenjing YangCollege of Medical Technology, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Yongxue YangGeriatric Diseases Institute of Chengdu/Cancer Prevention and Treatment Institute of Chengdu, Department of Clinical Trial Center, Chengdu Fifth People's Hospital (The Second Clinical Medical College, Affiliated Fifth People's Hospital of Chengdu University of Traditional Chinese Medicine), Chengdu, China.
Jinlin GuoCollege of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cerebral small vessel disease (CSVD) is a common cause of stroke and vascular cognitive impairment. It is urgent to find drugs targeting CSVD. This study explores the therapeutic potential of the flavonoid (DHBF) derived from Methods: Spontaneously hypertensive rats (24-weeks-old) were treated with DHBF for 8 weeks. The Morris water maze test, laser speckle contrast imaging, photoacoustic tomography, HE and Nissl staining were used to evaluate the effect of DHBF in CSVD rats. Network pharmacology and UPLC-MS were used to identify DHBF components and potential mechanisms. Human umbilical vein endothelial cells (HUVECs) were exposed to 10% O Results: DHBF alleviated vessel injury, improved learning and memory abilities, and increased cerebral blood perfusion and oxygen supply capacity in 24-week-old CSVD rats ( Conclusion: In summary, DHBF exerts a therapeutic effect on CSVD by inhibiting Ang2, regulating the Angs-Tie2 pathway, and inhibiting endothelial autophagy. This study proposed a potential effective target for CSVD, provided data to support subsequent drug development for this condition.

Indexed as

Angiogeninautophagycerebral small vessel diseaseflavonoid of Dracocephalum heterophyllum Benth.human umbilical vein endothelial cells

Identifiers

PMID40432894
PMCPMC12107102

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.