Audousset Camille, McGovern Toby, Martin James G
Meakins-Christie Laboratories, McGill University, Montréal, QC, Canada.
Front Physiol. 2021 Sep 29;12:727806. doi: 10.3389/fphys.2021.727806. eCollection 2021.
Nuclear factor erythroid 2-related factor 2 (Nrf2) is a major transcription factor involved in redox homeostasis and in the response induced by oxidative injury. Nrf2 is present in an inactive state in the cytoplasm of cells. Its activation by internal or external stimuli, such as infections or pollution, leads to the transcription of more than 500 elements through its binding to the antioxidant response element. The lungs are particularly susceptible to factors that generate oxidative stress such as infections, allergens and hyperoxia. Nrf2 has a crucial protective role against these ROS. Oxidative stress and subsequent activation of Nrf2 have been demonstrated in many human respiratory diseases affecting the airways, including asthma and chronic obstructive pulmonary disease (COPD), or the pulmonary parenchyma such as acute respiratory distress syndrome (ARDS) and pulmonary fibrosis. Several compounds, both naturally occurring and synthetic, have been identified as Nrf2 inducers and enhance the activation of Nrf2 and expression of Nrf2-dependent genes. These inducers have proven particularly effective at reducing the severity of the oxidative stress-driven lung injury in various animal models. In humans, these compounds offer promise as potential therapeutic strategies for the management of respiratory pathologies associated with oxidative stress but there is thus far little evidence of efficacy through human trials. The purpose of this review is to summarize the involvement of Nrf2 and its inducers in ARDS, COPD, asthma and lung fibrosis in both human and in experimental models.
核因子红细胞2相关因子2(Nrf2)是一种主要的转录因子,参与氧化还原稳态以及氧化损伤诱导的反应。Nrf2以无活性状态存在于细胞胞质中。其被内部或外部刺激(如感染或污染)激活后,通过与抗氧化反应元件结合,导致500多个元件的转录。肺对产生氧化应激的因素(如感染、过敏原和高氧)特别敏感。Nrf2对这些活性氧具有关键的保护作用。氧化应激以及随后Nrf2的激活已在许多影响气道的人类呼吸道疾病中得到证实,包括哮喘和慢性阻塞性肺疾病(COPD),或肺实质疾病如急性呼吸窘迫综合征(ARDS)和肺纤维化。几种天然和合成的化合物已被鉴定为Nrf2诱导剂,可增强Nrf2的激活和Nrf2依赖性基因的表达。这些诱导剂在各种动物模型中已被证明在减轻氧化应激驱动的肺损伤严重程度方面特别有效。在人类中,这些化合物有望成为治疗与氧化应激相关的呼吸道疾病的潜在治疗策略,但迄今为止,通过人体试验几乎没有疗效证据。本综述的目的是总结Nrf2及其诱导剂在人类和实验模型中ARDS、COPD、哮喘和肺纤维化中的作用。