ArticleFrontiers in pharmacology2025
Mechanism of Shenyuan Yiqi Huoxue capsule alleviating coronary microvascular dysfunction: network analysis and experimental evidence.
Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Shenyuan Yiqi Huoxue Capsule (SYYQ) has clinical evidence to improve coronary microvascular dysfunction (CMD) by tonifying qi and removing blood stasis, but the underlying mechanism remains unclear. Objective: This study aims to explore the mechanism by which SYYQ alleviates CMD through a combination of network analysis and both Methods: First, network pharmacology was employed to predict the mechanism of SYYQ on CMD. Building upon the findings of network pharmacology, we conducted Results: The results of network pharmacology suggest that SYYQ may enhance CMD through pathways related to apoptosis and vascular growth. Animal experiments demonstrated that SYYQ alleviated apoptosis, promoted microvascular opening, and reduced myocardial injury in CMD rats. Furthermore, cell experiments indicated that SYYQ mitigated apoptosis in hypoxic (Hyp) MCMECs, promoted the production of angiogenic factors. Furthermore, downregulation of miR-302-3p levels and activation of Hippo pathway were observed in Hyp MCMECs, which can be inhibited by SYYQ. When miR-302a-3p was overexpressed or the Hippo pathway was inhibited, the efficacy of SYYQ in promoting the production of angiogenic factors and inhibiting apoptosis in Hyp MCMECs was significantly enhanced. Additional studies revealed that miR-302a-3p negatively regulated LATS2. Conclusion: SYYQ improves CMD by promoting the production of angiogenic factors and inhibiting apoptosis via miR-302a-3p/Hippo.
Indexed as
Identifiers
What Socratic 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 Socratic graph.