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中风的基因治疗:2006年综述

Gene therapy for stroke: 2006 overview.

作者信息

Chu Yi, Miller Jordan D, Heistad Donald D

机构信息

Department of Internal Medicine, University of Iowa Carver College of Medicine, Iowa City, Iowa 52242, USA.

出版信息

Curr Hypertens Rep. 2007 Mar;9(1):19-24. doi: 10.1007/s11906-007-0005-7.

Abstract

Gene therapy is a promising approach for treatment of stroke and other cerebrovascular diseases, although it may take many years to realize. Gene therapy could occur prior to a stroke (eg, to stabilize atherosclerotic plaques) and/or following a stroke (eg, to prevent vasospasm after subarachnoid hemorrhage or reduce injury to neurons by ischemic insult). We have transferred the gene coding for vasoactive calcitonin gene-related peptide via cerebrospinal fluid, and demonstrated attenuation of vasospasm after SAH. Transfer of neuroprotective genes or small interfering RNA for neurotoxic genes has good potential for ischemic stroke. In this brief report, we review recent developments in experimental gene therapy for stroke. Fundamental advances, including development of safer, more specific gene transfer vectors, are discussed.

摘要

基因治疗是治疗中风和其他脑血管疾病的一种有前景的方法,尽管可能需要很多年才能实现。基因治疗可以在中风之前进行(例如,稳定动脉粥样硬化斑块)和/或中风之后进行(例如,预防蛛网膜下腔出血后的血管痉挛或减轻缺血性损伤对神经元的损害)。我们已经通过脑脊液转移了编码血管活性降钙素基因相关肽的基因,并证明了蛛网膜下腔出血后血管痉挛的减轻。神经保护基因或针对神经毒性基因的小干扰RNA的转移对缺血性中风具有良好的潜力。在这份简短的报告中,我们回顾了中风实验性基因治疗的最新进展。讨论了包括开发更安全、更特异的基因转移载体在内的基础进展。

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