Cardioprotective effects of simvastatin‑loaded nano‑niosomes on cardiomyocytes in cardiac ischemia

N. Aboutaleb, Mahdieh Mehrab Mohseni, Maryam Naseroleslami
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Abstract

Background. Cardiac ischemia is the major cause of morbidity and mortality which can be increased by Statins. This study aimed to increase the effectiveness of simvastatin in the form of niosomes. Methods. In this study, 25 male Wistar rats were divided into 5 groups: control, ischemia (induced by closed LAD), ischemia receiving nano-niosomes, ischemia receiving simvastatin, and ischemia receiving simvastatin-loaded nano-niosomes. One month after the drug injection, RNA was extracted from the heart tissue of the studied groups, cDNA was synthesized, and a real-time PCR test was performed using specific primers. SPSS 21.0 software was used for statistical analysis. Analysis of variance was used to investigate the effect of the interventions, and Tukey's post hoc test was used to investigate a significant difference (P<0.05) between the control groups and other groups as well as between intervention groups. Results. Apoptosis and autophagy increased significantly in the ischemia group compared to the control group (P<0.05). In the simvastatin-loaded nano-niosomes group, compared to the simvastatin group, apoptosis and autophagy showed a significant decrease (P<0.05), and also in both simvastatin-loaded nano-niosomes and simvastatin group, compared to the control group, apoptosis and autophagy showed a significant decrease. (P<0.05). Conclusion. Simvastatin is an effective drug in the recovery of cardiac ischemia, but the main problem in using simvastatin is its instability and degradability, and the use of its niosomes form solves this problem properly. Practical Implications. Simvastatin‑loaded nano‑niosomes is more effective in reducing heart ischemia damage compared to simvastatin.
辛伐他汀纳米粒对心肌细胞缺血的保护作用
背景。心脏缺血是发病率和死亡率的主要原因,他汀类药物可增加发病率和死亡率。本研究旨在提高辛伐他汀以纳米体形式的有效性。方法。本研究将25只雄性Wistar大鼠分为5组:对照组、缺血(封闭LAD诱导)组、缺血纳米粒组、缺血辛伐他汀组、缺血负载辛伐他汀纳米粒组。注射药物1个月后,从实验组心脏组织中提取RNA,合成cDNA,用特异性引物进行实时PCR检测。采用SPSS 21.0软件进行统计分析。采用方差分析考察干预措施的效果,采用Tukey事后检验考察对照组与其他组、干预组之间的差异有统计学意义(P<0.05)。结果。缺血组细胞凋亡和细胞自噬明显高于对照组(P<0.05)。与辛伐他汀组相比,负载辛伐他汀纳米粒组细胞凋亡和自噬均显著降低(P<0.05),负载辛伐他汀纳米粒组和辛伐他汀组细胞凋亡和自噬均显著降低(P<0.05)。(P < 0.05)。结论。辛伐他汀是一种有效的心脏缺血恢复药物,但辛伐他汀使用的主要问题是其不稳定性和可降解性,而其niosomes形式的使用很好地解决了这一问题。实际意义。与辛伐他汀相比,负载辛伐他汀的纳米小体在减少心脏缺血损伤方面更有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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