Evidence map›Paper›PMID 35950380›Full record

ArticleBeijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences2022

[Effects of 4'-O-methylochnaflavone on endothelial dysfunction induced by palmitic acid in rat cavernous endothelial cells].

Y Y Gu, X H Tan, W P Song, D Fang, W D Song, Y M Yuan, N H Feng, R L Guan

Open access · greenAbstract read
In one paragraph

Article in Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 81% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 2 institutions in 1 country.

Y Y GuDepartment of Urology, Peking University First Hospital; Institute of Urology, Peking University; Beijing 100034, China.
X H TanDepartment of Urology, Peking University First Hospital; Institute of Urology, Peking University; Beijing 100034, China.
W P SongDepartment of Urology, Peking University First Hospital; Institute of Urology, Peking University; Beijing 100034, China.
D FangDepartment of Urology, Peking University First Hospital; Institute of Urology, Peking University; Beijing 100034, China.
W D SongDepartment of Urology, Peking University First Hospital; Institute of Urology, Peking University; Beijing 100034, China.
Y M YuanDepartment of Urology, Peking University First Hospital; Institute of Urology, Peking University; Beijing 100034, China.
N H FengDepartment of Urology, Wuxi Second Hospital, Nanjing Medical University, Wuxi 214002, Jiangsu, China.
R L GuanDepartment of Urology, Peking University First Hospital; Institute of Urology, Peking University; Beijing 100034, China.
Peking University · CNWuxi People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the effect of biflavonoid 4'-O-methylochnaflavone (MF) on palmitic acid-induced endothelial dysfunction in rat cavernous endothelial cells (RCECs).

methodsThe isolated RCECs were commercially available and randomly divided into four groups: normal+BSA group (NC group), palmitic acid (PA) group, MF group, and icariside Ⅱ (ICA Ⅱ) group. The protein expression levels of protein kinase B (PKB/AKT) and endothelial nitric oxide synthase (eNOS) in each group were evaluated via Western blotting. The differences in the intracellular nitric oxide of RCECs treated by MF or ICA Ⅱ were detected by DAF-FM DA that served as a nitric oxide fluorescent probe. Effects of MF and ICA Ⅱ on cell proliferation of PA-stimulated RCECs were determined via CCK-8 assay.

resultsThe content of nitric oxide in RCECs was significantly increased after the treatment of MF and ICA Ⅱ in comparison with the NC group (

conclusionIn RCECs, MF and ICA Ⅱ could effectively increase the content of nitric oxide. The down-regulation of the expression of proteins associated with the AKT/eNOS pathway after PA treatment revealed that this pathway was involved in the development of endothelial dysfunction, which could be effectively reversed by MF and ICA Ⅱ. In addition, the cell proliferation ability was significantly decreased following PA treatment, but MF and ICA Ⅱ could restore the above changes. Overall, biflavonoid MF has an obvious repairing effect on PA-stimulated endothelial dysfunction.

Indexed as

BiflavonoidsProto-Oncogene Proteins c-aktAnimalsCells, CulturedEndothelial CellsNitric OxideNitric Oxide Synthase Type IIIPalmitic AcidPhosphorylationRatsSignal TransductionBiflavonoidsNitric OxideNitric Oxide Synthase Type IIIPalmitic AcidProto-Oncogene Proteins c-aktEndothelial dysfunctionNitric oxide synthasePalmitic acidSignal transduction

Identifiers

PMID35950380
PMCPMC9385526
OpenAlexW4291020283

What OpenQuestion holds

Textmetadata
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.