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心室修复和心肌再生的心脏支持生物假体的开发。

Development of cardiac support bioprostheses for ventricular restoration and myocardial regeneration.

机构信息

Department of Cardiovascular Surgery, Laboratory of Biosurgical Research, Pompidou Hospital, University Paris Descartes, Paris, France.

出版信息

Eur J Cardiothorac Surg. 2013 Jun;43(6):1211-9. doi: 10.1093/ejcts/ezs480. Epub 2012 Aug 31.

Abstract

OBJECTIVES

Ventricular constraint devices made of polyester and nitinol have been used to treat heart failure patients. Long-term follow-up has not demonstrated significant benefits, probably due to the lack of effects on myocardial tissue and to the risk of diastolic dysfunction. The goal of this experimental study is to improve ventricular constraint therapy by associating stem cell intrainfarct implantation and a cell-seeded collagen scaffold as an interface between the constraint device and the epicardium.

METHODS

In a sheep ischaemic model, three study groups were created: Group 1: coronary occlusion without treatment (control group). Group 2: postinfarct ventricular constraint using a polyester device (Acorn CorCap). Group 3: postinfarct treatment with stem cells associated with collagen matrix and the polyester device. Autologous adipose mesenchymal stem cells cultured in hypoxic conditions were injected into the infarct and seeded into the collagen matrix.

RESULTS

At 3 months, echocardiography showed the limitation of left ventricular end-diastolic volume in animals both treated with constraint devices alone and associated with stem cells/collagen. In Group 3 (stem cell + collagen treatment), significant improvements were found in ejection fraction (EF) and diastolic function evaluated by Doppler-derived mitral deceleration time. In this group, histology showed a reduction of infarct size, with focuses of angiogenesis and minimal fibrosis interface between CorCap and the epicardium due to the interposition of the collagen matrix.

CONCLUSIONS

Myocardial infarction treated with stem cells associated with a collagen matrix and ventricular constraint device improves systolic and diastolic function, reducing adverse remodelling and fibrosis. The application of bioactive molecules and the recent development of nanobiotechnologies should open the door for the creation of a new semi-degradable ventricular support bioprosthesis, capable of controlled stability or degradation in response to physiological conditions of the left or right heart.

摘要

目的

聚酯和镍钛诺制成的心室约束装置已被用于治疗心力衰竭患者。长期随访并未显示出显著的益处,这可能是由于对心肌组织的作用有限,以及舒张功能障碍的风险。本实验研究的目的是通过将干细胞梗死内植入和细胞接种胶原支架作为约束装置与心外膜之间的接口,来改善心室约束治疗。

方法

在绵羊缺血模型中,创建了三个研究组:第 1 组:无治疗的冠状动脉闭塞(对照组)。第 2 组:使用聚酯装置(Acorn CorCap)进行梗死后心室约束。第 3 组:梗死后联合使用干细胞和胶原基质与聚酯装置治疗。在缺氧条件下培养的自体脂肪间充质干细胞被注射到梗死部位并接种到胶原基质中。

结果

在 3 个月时,超声心动图显示单独使用约束装置和联合使用干细胞/胶原的动物的左心室舒张末期容积受限。在第 3 组(干细胞+胶原治疗组)中,射血分数(EF)和通过多普勒衍生的二尖瓣减速时间评估的舒张功能均有显著改善。在该组中,组织学显示梗死面积减小,由于胶原基质的介入,CorCap 和心外膜之间存在血管生成和最小纤维化界面。

结论

与胶原基质和心室约束装置联合使用的干细胞治疗可改善收缩和舒张功能,减少不良重塑和纤维化。生物活性分子的应用和纳米生物技术的最新发展应为创建一种新的半可降解心室支撑生物假体开辟道路,该假体能够根据左心或右心的生理条件,实现控制稳定性或降解。

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