Key result
Cardiotonic Pills reduce infarct size and restore blood flow in a pig model of ISR.
Why the study?
Stent implantation for obstructive coronary artery disease is frequently complicated by in-stent restenosis, leading this study to explore whether Cardiotonic Pills attenuate ISR-evoked myocardial injury and fibrosis.
Does Cardiotonic Pills® attenuate myocardial injury and fibrosis in a miniature pig model of in-stent restenosis?
Does Cardiotonic Pills® attenuate myocardial injury and fibrosis in a miniature pig model of in-stent restenosis?
In a miniature pig model, Cardiotonic Pills® protected against myocardial injury and fibrosis caused by in-stent restenosis, potentially by regulating energy metabolism and inhibiting the TGF β1/Smads signaling pathway.
Cardiotonic Pills® attenuates injury in porcine restenosis model; leaves open translation to human in-stent restenosis management.
BACKGROUND: Stent implantation has been increasingly applied for the treatment of obstructive coronary artery disease, which, albeit effective, often harasses patients by in-stent restenosis (ISR). PURPOSE: The present study was to explore the role of compound Chinese medicine Cardiotonic Pills® (CP) in attenuating ISR-evoked myocardial injury and fibrosis. STUDY DESIGN: Chinese miniature pigs were used to establish ISR model by implanting obsolete degradable stents into coronary arteries. Quantitative coronary angiography (QCA) was performed to confirm the success of the model. METHODS: CP was given at 0.2 g/kg daily for 30 days after ISR. On day 30 and 60 after stent implantation, the myocardial infarct and myocardial blood flow (MBF) were assessed. Myocardial histology was evaluated by hematoxylin-eosin and Masson's trichrome staining. The content of ATP, MPO, and the activity of mitochondrial respiratory chain complex Ⅳ were determined by ELISA. Western blot was performed to assess the expression of ATP5D and related signaling proteins, and the mediators of myocardial fibrosis. RESULTS: Treatment with CP diminished myocardial infarct size, retained myocardium structure, attenuated myocardial fibrosis, and restored MBF. CP ameliorated energy metabolism disorder, attenuated TGFβ1 up-regulation and reversed its downstream gene expression, such as Smad6 and Smad7, and inhibited the increased expression of MCP-1, PR S19, MMP-2 and MMP-9. CONCLUSION: CP effectively protects myocardial structure and function from ISR challenge, possibly by regulating energy metabolism via inactivation of RhoA/ROCK signaling pathway and inhibition of monocyte chemotaxis and TGF β1/Smads signaling pathway.
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Yan et al. (2022) studied In-stent restenosis-evoked myocardial injury and fibrosis. Cardiotonic Pills® was evaluated on Myocardial infarct size, myocardial blood flow, and myocardial fibrosis. Cardiotonic Pills (0.2 g/kg daily for 30 days) diminished myocardial infarct size, attenuated fibrosis, and restored myocardial blood flow in a miniature pig model of in-stent restenosis.
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