Evidence map›Paper›PMID 34985385›Full record

ArticlePharmaceutical biology2022

Network pharmacology and

Wei Zhang, Li Zhang, Wen Jun Wang, Shanbo Ma, Mingming Wang, Minna Yao, Ruili Li, Wei Wei Li, Xian Zhao, Dongmei Hu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.6field-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, 17 citations in OpenAlex.

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  12. Antidepressant effects of total alkaloids ofPharmaceutical biology · 2022
    Article
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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 2 institutions in 1 country.

Wei ZhangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Li ZhangDepartment of Emergency, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Wen Jun WangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Shanbo MaDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Mingming WangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Minna YaoDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Ruili LiDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Wei Wei LiDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Xian ZhaoDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Dongmei HuDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Yi DingDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Jingwen WangDepartment of Pharmacy, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
Air Force Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextStroke is an illness with high morbidity, disability and mortality that presents a major clinical challenge. Sanhua decoction (SHD) has been widely used to treat ischaemic stroke in the clinic. However, the potential mechanism of SHD remains unknown.

objectiveTo elucidate the multitarget mechanism of SHD in ischaemic stroke through network pharmacology and bioinformatics analyses. MATERIALS AND

methodsNetwork pharmacology and experimental validation approach was used to investigate the bioactive ingredients, critical targets and potential mechanisms of SHD against ischaemic stroke. Four herbal names of SHD, 'ischemic stroke' or 'stroke' was used as a keyword to search the relevant databases. SH-SY5Y cells were treated with various concentrations of SHD (12.5, 25, 50 or 100 μg/mL) for 4 h, exposed to oxygen and glucose deprivation (OGD) for 1 h, then reoxygenation for 24 h. The cell viability was detected by MTT, the lactate dehydrogenase (LDH) was evaluated by ELISA, and protein expression was detected by western blots.

resultsSHD treatment increased the survival rate from 65.9 ± 4.3 to 85.56 ± 5.7%. The median effective dose (ED DISCUSSION AND

conclusionsThis study suggests that SHD protects against cerebral ischaemic injury via regulation of the PI3K/Akt/CREB1 and TNF pathways.

Indexed as

ApoptosisBrain IschemiaCell Line, TumorCell SurvivalCyclic AMP Response Element-Binding ProteinDose-Response Relationship, DrugDrugs, Chinese HerbalHumansIschemic StrokeNetwork PharmacologyNeuroblastomaPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktTumor Necrosis Factor-alphaCREB1 protein, humanCyclic AMP Response Element-Binding ProteinDrugs, Chinese HerbalPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktTNF protein, humanTumor Necrosis Factor-alphacell viabilityCerebral ischaemiamolecular dockingSH-SY5Y cells

Identifiers

PMID34985385
PMCPMC8741256
OpenAlexW4205383956

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.