Berezowski Vincent, Fukuda Andrew M, Cecchelli Roméo, Badaut Jérôme
Université Lille Nord de France, 59000 Lille, France.
Int J Cell Biol. 2012;2012:176287. doi: 10.1155/2012/176287. Epub 2012 Jun 24.
The neurovascular/gliovascular unit has recently gained increased attention in cerebral ischemic research, especially regarding the cellular and molecular changes that occur in astrocytes and endothelial cells. In this paper we summarize the recent knowledge of these changes in association with edema formation, interactions with the basal lamina, and blood-brain barrier dysfunctions. We also review the involvement of astrocytes and endothelial cells with recombinant tissue plasminogen activator, which is the only FDA-approved thrombolytic drug after stroke. However, it has a narrow therapeutic time window and serious clinical side effects. Lastly, we provide alternative therapeutic targets for future ischemia drug developments such as peroxisome proliferator- activated receptors and inhibitors of the c-Jun N-terminal kinase pathway. Targeting the neurovascular unit to protect the blood-brain barrier instead of a classical neuron-centric approach in the development of neuroprotective drugs may result in improved clinical outcomes after stroke.
神经血管/胶质血管单元最近在脑缺血研究中受到越来越多的关注,特别是关于星形胶质细胞和内皮细胞中发生的细胞和分子变化。在本文中,我们总结了与水肿形成、与基膜的相互作用以及血脑屏障功能障碍相关的这些变化的最新知识。我们还回顾了星形胶质细胞和内皮细胞与重组组织型纤溶酶原激活剂的关系,重组组织型纤溶酶原激活剂是美国食品药品监督管理局批准的唯一一种中风后溶栓药物。然而,它的治疗时间窗狭窄且有严重的临床副作用。最后,我们为未来缺血性药物开发提供了替代治疗靶点,如过氧化物酶体增殖物激活受体和c-Jun氨基末端激酶途径抑制剂。在神经保护药物开发中,以神经血管单元为靶点来保护血脑屏障,而不是采用传统的以神经元为中心的方法,可能会改善中风后的临床结果。