Key result
Colchicine nanoparticles reduce infarct size ~45% and attenuate fibrosis in a rat MI model.
Why the study?
New anti-inflammatory drugs and their mechanisms are necessary to be explored to improve clinical efficacy in reducing myocardial injury after acute myocardial infarction.
Does colchicine-containing calcium carbonate nanoparticles reduce myocardial infarct size and inflammation in a rat model of acute myocardial infarction?
Does colchicine-containing calcium carbonate nanoparticles reduce myocardial infarct size and inflammation in a rat model of acute myocardial infarction?
Colchicine-containing calcium carbonate nanoparticles attenuate myocardial infarction injury and inflammation in a rat model, suggesting a potential novel delivery system for cardioprotection.
Answers are grounded in this paper and cite their sources.
Supports preclinical optimization of nanoparticle colchicine; leaves open safety and efficacy in human acute MI.
Purpose Anti-inflammatory therapy is important for reducing myocardial injury after acute myocardial infarction (MI). New anti-inflammatory drugs and their mechanism are necessary to be explored to improve the clinical efficacy. We aimed to improve the efficacy of colchicine on attenuating MI injury by nano-drug delivery systems, and to investigate the mechanism of anti-inflammatory. Methods Colchicine-containing delivery system based on calcium carbonate nanoparticles (ColCaNPs) was synthesized. The protection against MI by ColCaNPs was evaluated using an in vivo rat model established by ligating the left anterior descending coronary artery. Macrophage polarization and the levels of inflammatory cytokines were determined using immunohistochemistry, western blot and ELISA analysis. Results ColCaNPs treatment showed about a 45% reduction in myocardial infarct size and attenuating myocardial fibrosis compared with groups without drug intervention after MI. Furthmore, ColCaNPs significantly decreased the levels of CRP, TNF-α and IL-1β in serum and the expression of proinflammatory cytokine in myocardial tissues after MI (p < 0.05). We also found that ColCaNPs notably restrained pyroptosis, and inhibited inflammatory response by modulating on M1/M2 macrophage polarization and suppressing TLR4/NFκB/NLRP3 signal pathway. Conculsion Colchicine-containing nanoparticles can protect against MI injury in a clinically relevant rat model by reducing inflammation. In addition, calcium carbonate nanoparticles can increase the cardioprotective effects of colchicine.
No takes yet. Share an insight, caveat, or question.
Wang et al. (2021) studied Acute myocardial infarction (n=30). Colchicine-containing calcium carbonate nanoparticles (ColCaNPs) vs. No drug intervention (MI group), free colchicine, or empty nanoparticles was evaluated on Myocardial infarct size (45% reduction, p=<0.05). Colchicine-containing nanoparticles reduced myocardial infarct size by 45% and attenuated myocardial fibrosis compared to no drug intervention in a rat model of acute myocardial infarction.
Synapse has enriched 8 closely related papers on similar clinical questions. Consider them for comparative context: