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基因和细胞治疗的生物学起搏。

Biological pacing by gene and cell therapy.

机构信息

Heart Failure Research Centre, Academic Medical Centre, University of Amsterdam, Amsterdam, and Interuniversity Cardiology Institute Netherlands, Utrecht, the Netherlands.

出版信息

Neth Heart J. 2007;15(9):318-22. doi: 10.1007/BF03086008.

DOI:10.1007/BF03086008
PMID:18604282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2442912/
Abstract

At present, cardiac rhythm disorders such as sick sinus syndrome (SSS) or AV nodal block (AVB) are usually treated by electronic pacemakers. These devices have significant shortcomings, including lack of autonomic modulation, and the need for repetitive procedures for battery replacement or lead repositioning. Biological pacemakers as replacement or complement to electronic pacemakers have been the subject of increasing research interest. This research has resulted in many encouraging preclinical studies. Various approaches in the field of gene and cell therapy have been developed by different groups and this combined effort makes it increasingly realistic that this therapy will eventually find its way to clinical applicability. (Neth Heart J 2007;15:318-22.).

摘要

目前,心脏节律紊乱,如窦性心动过缓(SSS)或房室传导阻滞(AVB)通常采用电子起搏器进行治疗。这些设备存在显著缺陷,包括缺乏自主调节功能,需要重复进行电池更换或导线重新定位等程序。生物起搏器作为电子起搏器的替代品或补充物,已成为越来越多研究的课题。不同研究小组在基因和细胞治疗领域开展了各种方法的研究,这些共同的努力使得这种治疗方法最终实现临床应用的可能性越来越大。(Neth Heart J 2007;15:318-22.)

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本文引用的文献

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Pacemaker current (I(f)) in the human sinoatrial node.人类窦房结中的起搏电流(I(f))
Eur Heart J. 2007 Oct;28(20):2472-8. doi: 10.1093/eurheartj/ehm339. Epub 2007 Sep 6.
2
Finding fluorescent needles in the cardiac haystack: tracking human mesenchymal stem cells labeled with quantum dots for quantitative in vivo three-dimensional fluorescence analysis.在心脏“干草堆”中寻找荧光针:追踪用量子点标记的人间充质干细胞用于体内定量三维荧光分析。
Stem Cells. 2007 Aug;25(8):2128-38. doi: 10.1634/stemcells.2006-0722. Epub 2007 May 10.
3
Bioartificial sinus node constructed via in vivo gene transfer of an engineered pacemaker HCN Channel reduces the dependence on electronic pacemaker in a sick-sinus syndrome model.通过工程化起搏器HCN通道的体内基因转移构建的生物人工窦房结可降低病态窦房结综合征模型对电子起搏器的依赖。
Circulation. 2006 Sep 5;114(10):1000-11. doi: 10.1161/CIRCULATIONAHA.106.615385. Epub 2006 Aug 21.
4
Wild-type and mutant HCN channels in a tandem biological-electronic cardiac pacemaker.串联式生物电子心脏起搏器中的野生型和突变型HCN通道
Circulation. 2006 Sep 5;114(10):992-9. doi: 10.1161/CIRCULATIONAHA.106.617613. Epub 2006 Aug 21.
5
Recombinant adeno-associated virus serotype 9 leads to preferential cardiac transduction in vivo.重组腺相关病毒9型在体内可导致心脏优先转导。
Circ Res. 2006 Aug 18;99(4):e3-9. doi: 10.1161/01.RES.0000237661.18885.f6. Epub 2006 Jul 27.
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Potential of stem-cell-based therapies for heart disease.基于干细胞的心脏病治疗方法的潜力。
Nature. 2006 Jun 29;441(7097):1097-9. doi: 10.1038/nature04961.
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