Evidence map›Paper›PMID 33962551›Full record

ArticlePharmaceutical biology2021

Potential mechanism of

Ji-Sheng Wang, Jun-Long Feng, Heng-Heng Dai, Zi-Long Chen, Xiao Li, Bing-Hao Bao, Sheng Deng, Fan-Chao Meng, Qi Zhao, Hong-Sheng Xu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Ji-Sheng WangFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Jun-Long FengFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Heng-Heng DaiFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Zi-Long ChenFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Xiao LiThe First Affiliated Hospital, Henan University of Chinese Medicine, Zhengzhou, Henan, China.
Bing-Hao BaoFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Sheng DengFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Fan-Chao MengFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Qi ZhaoFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Hong-Sheng XuFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, China.
Bin WangAndrology Department, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Hai-Song LiAndrology Department, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine · CNBeijing University of Chinese Medicine · CNFirst Affiliated Hospital of Henan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

context

objectiveExplore mechanistic details of ABR + SV treatment against DMED. MATERIALS AND

methodsPrediction of key targets by network pharmacology. A rat model of DM was established by streptozotocin injection (55 mg/kg). Apomorphine (100 μg/kg) was injected into rats to screen the DMED model. Group C (

resultsThe predicted key targets are albumin (ALB), caspase-3 (CASP3), vascular endothelial growth factor A (VEGFA), angiotensin-converting enzyme (ACE), and endothelial nitric oxide synthase (eNOS). Compared with the M group (0.52 ± 0.04; 0.50 ± 0.03; 0.49 ± 0.02; 0.23 ± 0.03), CASP3, VEGFA, and ACE protein expression reduced in the T group (0.39 ± 0.06; 0.34 ± 0.03; 0.39 ± 0.03), and eNOS protein expression increased (0.34 ± 0.03).

conclusionABR + SV can improve erectile function in DMED rats. This study provides a potential mechanism for the treatment of DMED with ABR + SV and can benefit from more patients.

Indexed as

AchyranthesVaccariaAnimalsDiabetes Mellitus, ExperimentalDisease Models, AnimalErectile DysfunctionMaleNetwork PharmacologyPlant ExtractsRatsRats, Sprague-DawleyTreatment OutcomePlant Extractsbiological networkEndocrine diseasespenistraditional Chinese medicine

Identifiers

PMID33962551
PMCPMC8118505
OpenAlexW3157314655

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.