ArticleMedicine2026
Comprehensive network pharmacology study on Huangjing Wan in the treatment of ischaemic stroke.
Article in Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
Stroke is a leading cause of death and disability worldwide, with ischemic strokes accounting for the majority of cases. Huangjing Wan (HJW) is a classical Chinese herbal formula used in the treatment of stroke, but the precise mechanisms of action remain unclear. We retrieved the active components of HJW, along with their related targets and the targets associated with middle cerebral artery occlusion (MCAO), by conducting a search across relevant databases. The common targets obtained from the intersection of the 2 target sets were used to establish both a compound-target interaction network and a protein-protein interaction (PPI) network. A Kyoto Encyclopedia of Genes and Genomes (KEGG) bioinformatic analysis was ultimately performed to identify the potential signaling pathways associated with HJW in the treatment of MCAO. Through searching and screening a series of databases, we identified 129 active ingredient-associated targets of HJW and 1246 therapeutic targets for MCAO. The intersection of the 2 sets yielded 40 overlapping targets. Based on these 40 common targets, a compound-target interaction network and a PPI network were constructed. Finally, KEGG pathway enrichment analysis revealed that the key signaling pathways potentially involved in HJW treatment of MCAO primarily include the Hepatitis B pathway, the lipid and atherosclerosis pathway, and the Apoptosis pathway. This study reveals that HJW primarily exerts its therapeutic effects on MCAO through the Hepatitis B virus pathway, the lipid and atherosclerosis pathway, and the apoptosis pathway, providing a theoretical basis for further in-depth research.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.