Maniatis Nikolaos A, Orfanos Stylianos E
M. Simou Laboratory, University of Athens Medical School, Athens, Greece.
Curr Opin Crit Care. 2008 Feb;14(1):22-30. doi: 10.1097/MCC.0b013e3282f269b9.
Since pulmonary edema from increased endothelial permeability is the hallmark of acute lung injury, a frequently encountered entity in critical care medicine, the study of endothelial responses in this setting is crucial to the development of effective endothelial-targeted treatments.
From the enormous amount of research in the field of endothelial pathophysiology, we have focused on work delineating endothelial alterations elicited by noxious stimuli implicated in acute lung injury. The bulk of the material covered deals with molecular and cellular aspects of the pathogenesis, reflecting current trends in the published literature. We initially discuss pathways of endothelial dysfunction in acute lung injury and then cover the mechanisms of endothelial protection. Several experimental treatments in animal models are presented, which aid in the understanding of the disease pathogenesis and provide evidence for potentially useful therapies.
Mechanistic studies have delivered several interventions, which are effective in preventing and treating experimental acute lung injury and have thus provided objectives for translational studies. Some of these modalities may evolve into clinically useful tools in the treatment of this devastating illness.
由于内皮通透性增加所致的肺水肿是急性肺损伤的标志,急性肺损伤是重症医学中常见的病症,因此研究这种情况下的内皮反应对于开发有效的内皮靶向治疗至关重要。
在内皮病理生理学领域的大量研究中,我们重点关注了阐述由急性肺损伤相关有害刺激引起的内皮改变的研究。所涵盖的大部分内容涉及发病机制的分子和细胞方面,反映了已发表文献的当前趋势。我们首先讨论急性肺损伤中内皮功能障碍的途径,然后涵盖内皮保护机制。介绍了动物模型中的几种实验性治疗方法,这有助于理解疾病发病机制并为潜在的有效治疗提供证据。
机制研究已经提供了几种干预措施,这些措施可有效预防和治疗实验性急性肺损伤,因此为转化研究提供了目标。其中一些方法可能会发展成为治疗这种毁灭性疾病的临床有用工具。