Shah Imtiaz M, Macrae I Mhairi, Di Napoli Mario
Department of Medicine for the Elderly, Mansionhouse Unit, Victoria Infirmary, Glasgow, Scotland, G41 3DX, UK.
Curr Mol Med. 2009 Apr;9(3):336-54. doi: 10.2174/156652409787847236.
Cerebrovascular disease is one of the commonest causes of disability and mortality worldwide. Over the past two decades, a tremendous amount of research has been undertaken into developing effective therapeutic strategies for the treatment of acute stroke. Unfortunately, many neuroprotective agents that have shown successful results in treating animal models of acute stroke have failed to translate into clinical treatments. Only tissue-plasminogen activator (t-PA) is currently licensed for use in the treatment of acute ischaemic stroke. One of the important pathophysiological mechanisms involved during the acute phase of stroke is neuroinflammation. This review article will discuss the molecular aspects of neuroinflammation in acute ischaemic stroke and potential therapeutic strategies as part of translational medicine research.
脑血管疾病是全球致残和致死的最常见原因之一。在过去二十年中,为开发治疗急性中风的有效治疗策略进行了大量研究。不幸的是,许多在治疗急性中风动物模型中显示出成功结果的神经保护剂未能转化为临床治疗方法。目前只有组织型纤溶酶原激活剂(t-PA)被批准用于治疗急性缺血性中风。中风急性期涉及的重要病理生理机制之一是神经炎症。作为转化医学研究的一部分,这篇综述文章将讨论急性缺血性中风中神经炎症的分子方面以及潜在的治疗策略。