Evidence map›Paper›PMID 38515838›Full record

ArticleFrontiers in pharmacology2024

Pharmacological effects and target analysis of Guipi wan in the treatment of cerebral ischemia-reperfusion injury.

Jianfeng Zhang, Li Luo, Yanyan Guo, An Liu, Mengjia Zhang, Wei Jiang, Xi Li, Qingqing Liu, Jiaoyan Yu

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Jianfeng Zhang *Department of Pharmacy, Eighth Hospital of Xi'an City, Xi'an, China.
Li Luo *Department of Pharmacy, The Second Affiliated Hospital of Air Force Medical University, Xi'an, China.
Yanyan GuoDepartment of Pharmacy, The Second Affiliated Hospital of Air Force Medical University, Xi'an, China.
An LiuDepartment of Pharmacy, The Second Affiliated Hospital of Air Force Medical University, Xi'an, China.
Mengjia ZhangAir Force Medical University, Xi'an, China.
Wei JiangDepartment of Pharmacy, The Second Affiliated Hospital of Air Force Medical University, Xi'an, China.
Xi LiDepartment of Pharmacy, The Second Affiliated Hospital of Air Force Medical University, Xi'an, China.
Qingqing LiuDepartment of Pharmacy, The Second Affiliated Hospital of Air Force Medical University, Xi'an, China.
Jiaoyan YuDepartment of Pharmacy, The Second Affiliated Hospital of Air Force Medical University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Guipi wan (GPW) is a traditional Chinese medicine commonly used in clinical practice, typically to treat neurological diseases such as neurasthenia and traumatic brain injury. It may have positive effects on cerebral ischemia‒reperfusion injury (cI/R). This study aimed to assess the effects of GPW in a mouse model of cI/R and find its possible targets. C57BL/6J mice were used to establish the cI/R model, and the laser speckle doppler was used to determine the success of the model. GPW was administered intragastrically for 7 days, brain tissue sections were stained with TTC, HE, and TUNEL, Western blot assay was performed to detect the effect of apoptosis-related proteins. Furthermore, we screened active ingredients from the TCM Database and constructed a compound‒target network using the Cytoscape 3.8.0 software. Moreover, we employed protein‒protein interaction and component‒target‒pathway network analyses to determine the potential components of GPW and its target genes, the key target was verified through molecular docking. Finally, we detected the influence of the downstream signaling pathway of the target through Western blot. The results showed that GPW decreased the cerebral infarction area, neurological function scores, and neuronal apoptosis in mice by regulating PI3K/AKT signaling pathway. Network analysis indicated that gamma-aminobutyric acid B receptor 1 (GABBR1) might be a potential target for the treatment of cI/R. Molecular docking indicated that 9 active components in GPW could bind to GABBR1 with desirable binding energy. This study represented the demonstratable effect of GPW in the treatment of cI/R injury and suggested GABBR1 as a potential target using network analysis.

Indexed as

GABBR1guipi wanischemia-reperfusion injurynetwork analysisPI3K/AKT

Identifiers

PMID38515838
PMCPMC10955136

What Socratic 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 Socratic graph.