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氧化应激与哮喘和慢性阻塞性肺疾病中的基因转录:抗氧化治疗靶点

Oxidative stress and gene transcription in asthma and chronic obstructive pulmonary disease: antioxidant therapeutic targets.

作者信息

Rahman Irfan

机构信息

ELEGI Laboratory, MRC Centre for Inflammation Research, Medical School, University of Edinburgh, Edinburgh, UK.

出版信息

Curr Drug Targets Inflamm Allergy. 2002 Sep;1(3):291-315. doi: 10.2174/1568010023344607.

Abstract

Inflammatory lung diseases such as asthma and Chronic Obstructive Pulmonary Disease (COPD) are characterised by systemic and local chronic inflammation and oxidative stress. The sources of the increased oxidative stress in patients with asthma and COPD derive from the increased burden of inhaled oxidants, and from the increased amounts of reactive oxygen species (ROS) generated by several inflammatory, immune and structural cells of the airways. Increased levels of ROS produced in the airways are reflected by increased markers of oxidative stress in the airspaces, sputum, breath, lungs and blood in patients with asthma and COPD. ROS, either directly or via the formation of lipid peroxidation products such as acrolein, 4-hydroxy-2-nonenal and F(2)-isoprostanes, may play a role in enhancing the inflammation through the activation of stress kinases (JNK, MAPK, p38, phosphoinositide 3 (PI-3)-kinase/PI-3K-activated serine-threonine kinase Akt) and redox sensitive transcription factors such as NF-kappaB and AP-1. Recent data have also indicated that oxidative stress and pro-inflammatory mediators can alter nuclear histone acetylation/deacetylation allowing access for transcription factor DNA binding leading to enhanced pro-inflammatory gene expression in various lung cells. Furthermore, oxidative stress may alter the balance between gene expression of pro-inflammatory mediators and antioxidant enzymes in favor of inflammatory mediators in the lung. Thus, the presence of oxidative stress may have important consequences for the pathogenesis of asthma and COPD. Identification of genes that predispose to the development of asthma and COPD may identify novel therapeutic targets. Future work is directed to understand the molecular mechanisms of antioxidants on ROS-mediated cell signaling pathways and inhibition of inflammatory response that would provide information for the development of novel antioxidant therapeutic targets in asthma and COPD. Effective wide spectrum antioxidant therapy that has good bioavailability and potency is urgently needed to control the localised oxidative and inflammatory processes that occur in the pathogenesis of asthma and COPD. In addition, development of such novel antioxidant compounds would be therapeutically useful in monitoring the oxidative and inflammatory biomarkers in the progression/severity of asthma and COPD.

摘要

诸如哮喘和慢性阻塞性肺疾病(COPD)等炎症性肺病的特征是全身性和局部性慢性炎症以及氧化应激。哮喘和COPD患者氧化应激增加的来源包括吸入氧化剂负担的增加,以及气道中多种炎症、免疫和结构细胞产生的活性氧(ROS)数量的增加。哮喘和COPD患者气道中产生的ROS水平升高,表现为气腔、痰液、呼出气体、肺部和血液中氧化应激标志物的增加。ROS可直接或通过形成脂质过氧化产物(如丙烯醛、4-羟基-2-壬烯醛和F(2)-异前列腺素),通过激活应激激酶(JNK、MAPK、p38、磷酸肌醇3(PI-3)激酶/PI-3K激活的丝氨酸-苏氨酸激酶Akt)和氧化还原敏感转录因子(如NF-κB和AP-1)来增强炎症反应。最近的数据还表明,氧化应激和促炎介质可改变核组蛋白的乙酰化/去乙酰化,使转录因子能够结合DNA,从而导致各种肺细胞中促炎基因表达增强。此外,氧化应激可能会改变促炎介质和抗氧化酶基因表达之间的平衡,使肺部更倾向于炎症介质。因此,氧化应激的存在可能对哮喘和COPD的发病机制产生重要影响。识别易患哮喘和COPD的基因可能会确定新的治疗靶点。未来的工作旨在了解抗氧化剂对ROS介导的细胞信号通路的分子机制以及对炎症反应的抑制作用,这将为开发哮喘和COPD新的抗氧化治疗靶点提供信息。迫切需要一种具有良好生物利用度和效力的有效广谱抗氧化疗法,以控制哮喘和COPD发病机制中发生的局部氧化和炎症过程。此外,开发此类新型抗氧化化合物在监测哮喘和COPD进展/严重程度中的氧化和炎症生物标志物方面将具有治疗用途。

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