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中风基因治疗的未来。

The future of gene therapy for stroke.

作者信息

Gunnett C A, Heistad D D

机构信息

E315B-GH Department of Internal Medicine, University of Iowa College of Medicine, Iowa City 52242-1081, USA.

出版信息

Curr Hypertens Rep. 2001 Feb;3(1):36-40. doi: 10.1007/s11906-001-0076-9.

Abstract

New diagnostic and treatment strategies are being developed for stroke. Gene therapy has several potential advantages over classical pharmacologic therapy. Direct administration of DNA into the brain offers the advantage of producing high concentrations of therapeutic agents in a relatively localized environment. Gene transfer also provides longer duration of effect than traditional drug therapy. Recent studies indicate that gene transfer can produce functional proteins in brain parenchyma and cerebral blood vessels after stroke. In animal models, gene transfer may reduce effects of cerebral ischemia or subarachnoid hemorrhage. This review summarizes some current methods of gene transfer to the brain and recent progress that may lead to gene therapy for stroke.

摘要

针对中风正在开发新的诊断和治疗策略。与传统药物治疗相比,基因治疗有几个潜在的优势。将DNA直接注入大脑具有在相对局部的环境中产生高浓度治疗剂的优势。基因转移产生的效果持续时间也比传统药物治疗更长。最近的研究表明,中风后基因转移可在脑实质和脑血管中产生功能性蛋白质。在动物模型中,基因转移可能会减轻脑缺血或蛛网膜下腔出血的影响。本综述总结了目前一些将基因转移至大脑的方法以及可能导致中风基因治疗的最新进展。

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