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可生物降解的聚合物纳米胶囊可预防抗锥虫 Lychnopholide 的心脏毒性。

Biodegradable Polymeric Nanocapsules Prevent Cardiotoxicity of Anti-Trypanosomal Lychnopholide.

机构信息

Pharmaceutical Sciences Post-graduation Program (CiPharma), Escola de Farmácia, Universidade Federal de Ouro Preto, Minas Gerais, Brazil.

PHYMEDEXP, Inserm U1046, CNRS UMR 9214, Université de Montpellier - Montpellier, France.

出版信息

Sci Rep. 2017 Mar 28;7:44998. doi: 10.1038/srep44998.

Abstract

Chagas disease is a neglected parasitic disease caused by the protozoan Trypanosoma cruzi. New antitrypanosomal options are desirable to prevent complications, including a high rate of cardiomyopathy. Recently, a natural substance, lychnopholide, has shown therapeutic potential, especially when encapsulated in biodegradable polymeric nanocapsules. However, little is known regarding possible adverse effects of lychnopholide. Here we show that repeated-dose intravenous administration of free lychnopholide (2.0 mg/kg/day) for 20 days caused cardiopathy and mortality in healthy C57BL/6 mice. Echocardiography revealed concentric left ventricular hypertrophy with preserved ejection fraction, diastolic dysfunction and chamber dilatation at end-stage. Single cardiomyocytes presented altered contractility and Ca handling, with spontaneous Ca waves in diastole. Acute in vitro lychnopholide application on cardiomyocytes from healthy mice also induced Ca handling alterations with abnormal RyR2-mediated diastolic Ca release. Strikingly, the encapsulation of lychnopholide prevented the cardiac alterations induced in vivo by the free form repeated doses. Nanocapsules alone had no adverse cardiac effects. Altogether, our data establish lychnopholide presented in nanocapsule form more firmly as a promising new drug candidate to cure Chagas disease with minimal cardiotoxicity. Our study also highlights the potential of nanotechnology not only to improve the efficacy of a drug but also to protect against its adverse effects.

摘要

恰加斯病是一种由原生动物克氏锥虫引起的被忽视的寄生虫病。需要新的抗锥虫药物来预防并发症,包括高心肌病发生率。最近,一种天然物质,夏至草酚,显示出治疗潜力,特别是在包封在可生物降解的聚合物纳米胶囊中时。然而,关于夏至草酚可能的不良反应知之甚少。在这里,我们表明,重复静脉内给予游离夏至草酚(2.0mg/kg/天)20 天会导致健康 C57BL/6 小鼠的心肌病和死亡率。超声心动图显示末期出现同心性左心室肥厚伴射血分数保留、舒张功能障碍和心室扩张。单个心肌细胞表现出收缩力和 Ca 处理改变,舒张期出现自发性 Ca 波。急性体外应用夏至草酚也会导致健康小鼠心肌细胞 Ca 处理改变,伴有异常 RyR2 介导的舒张期 Ca 释放。引人注目的是,游离形式重复剂量体内诱导的心脏改变可被纳米胶囊包封的夏至草酚所预防。纳米胶囊本身对心脏没有不良影响。总之,我们的数据表明,纳米胶囊形式的夏至草酚更能成为一种有前途的新药物候选物,用于治疗恰加斯病,且心脏毒性最小。我们的研究还强调了纳米技术不仅可以提高药物的疗效,还可以防止其不良反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/673d/5368638/b2c553a37b2c/srep44998-f1.jpg

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