摘要
本文综述了肺动脉高压(PAH),一种无法治愈的疾病,它决定了很高的发病率和死亡率。疾病的定义、特征、分类和EP讨论了电动力学。由于缺乏症状特异性,PAH很难诊断。超声心动图及心电图对诊断的帮助在疾病的后续治疗中。然而,右心室(RV)导尿是诊断PAH的金标准。氧化应激和炎症,以一种互动的方式,在肺血管重塑的发展过程中,肺动脉压力的增加起着重要的作用。后者导致RV后负荷增加,最终导致RV肥大。可能会走向失败。临床和实验研究都显示氧化应激和炎症增加,不仅在肺和肺血管,而且在RV。e的使用实验模型,如野百合碱诱导的PAH,有助于理解PAH的病理生理学,以及开发新的治疗策略。除了传统的治疗学,使用能够调节氧化应激和炎症的治疗干预措施,可能为预防和管理这种疾病提供新的策略。
关键词: 肺动脉高压,氧化应激,炎症,单瓣花叶碱,氧化还原稳态,发病机制。
Current Medicinal Chemistry
Title:Role of Redox Homeostasis and Inflammation in the Pathogenesis of Pulmonary Arterial Hypertension
Volume: 25 Issue: 11
关键词: 肺动脉高压,氧化应激,炎症,单瓣花叶碱,氧化还原稳态,发病机制。
摘要: This review addresses pulmonary arterial hypertension (PAH), an incurable disease, which determines high morbidity and mortality. Definition of the disease, its characteristics, classification, and epidemiology are discussed. A difficulty in the diagnosis of PAH due to the lack of symptoms specificity is highlighted. Echocardiographic analysis and electrocardiogram of patients help in the diagnosis and in the follow up of the disease. Nevertheless, right ventricle (RV) catheterization constitutes the gold standard for diagnosing PAH. Oxidative stress and inflammation, in an interactive manner, play a major role in the development of pulmonary vascular remodeling and consequent increase of pulmonary pressure. The latter results in an increase in RV afterload, culminating with RV hypertrophy, which may progress to failure. Both clinical and experimental studies have shown increased oxidative stress and inflammation, not only in lungs and pulmonary vasculature but also in RV. The use of experimental models, such as the monocrotaline-induced PAH, has helped in the understanding of the pathophysiology of PAH, as well as in the development of new therapeutic strategies. In addition to the traditional therapeutics, the use of therapeutic interventions capable of modulating oxidative stress and inflammation may offer newer strategies in the prevention as well as management of this disease.
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Cite this article as:
Role of Redox Homeostasis and Inflammation in the Pathogenesis of Pulmonary Arterial Hypertension, Current Medicinal Chemistry 2018; 25 (11) . https://dx.doi.org/10.2174/0929867325666171226114838
DOI https://dx.doi.org/10.2174/0929867325666171226114838 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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