Crobeddu Emanuela, Pilloni Giulia, Tardivo Valentina, Fontanella Marco M, Panciani Pier P, Spena Giannantonio, Fornaro Riccardo, Altieri Roberto, Agnoletti Alessandro, Ajello Marco, Zenga Francesco, Ducati Alessandro, Garbossa Diego
Division of Neurosurgery, Department of Neurological Sciences, University of Turin, Turin, Italy -
J Neurosurg Sci. 2016 Sep;60(3):385-91. Epub 2015 Jan 20.
Cerebral vasospasm represents the most critical event that could occur after subarachnoid hemorrhage (SAH). Therapy is only partially effective because cerebral arterial constriction is not fully understood yet. One of the most important biological messenger associated to SAH is nitric oxide (NO), that is considered local regulator of cerebral blood flow. Different nitric oxide synthase (NOS) forms play a role in different biological processes, one of which is to link neuronal activity to blood flow in cerebral cortex. We performed a reassessment of the literature to summarize the role of NO as the main inflammatory pathway activated after SAH to clarify its importance for treatment of vasospasm.
脑血管痉挛是蛛网膜下腔出血(SAH)后可能发生的最关键事件。由于对脑动脉收缩的机制尚未完全了解,目前的治疗仅部分有效。与SAH相关的最重要生物信使之一是一氧化氮(NO),它被认为是脑血流的局部调节因子。不同形式的一氧化氮合酶(NOS)在不同的生物学过程中发挥作用,其中之一是将神经元活动与大脑皮层的血流联系起来。我们重新评估了文献,以总结NO作为SAH后激活的主要炎症途径的作用,从而阐明其在血管痉挛治疗中的重要性。