Ahmad Shabir, Saleem Muhammad, Riaz Naheed, Lee Yong Sup, Diri Reem, Noor Ahmad, Almasri Diena, Bagalagel Alaa, Elsebai Mahmoud Fahmi
Department of Chemistry, Baghdad-ul-Jadeed Campus, The Islamia University of Bahawalpur, Bahawalpur, Pakistan.
Department of Chemistry, Post-Graduate College, Bahawalpur, Pakistan.
Front Pharmacol. 2020 Jun 5;11:688. doi: 10.3389/fphar.2020.00688. eCollection 2020.
Human neutrophil elastase (HNE) is a major cause of the destruction of tissues in cases of several different chronic andinflammatory diseases. Overexpression of the elastase enzyme plays a significant role in the pathogenesis of various diseases including chronic obstructive pulmonary disease (COPD), acute respiratory distress syndrome, rheumatoid arthritis, the rare disease cyclic hematopoiesis (or cyclic neutropenia), infections, sepsis, cystic fibrosis, myocardial ischemia/reperfusion injury and asthma, inflammation, and atherosclerosis. Human neutrophil elastase is secreted by human neutrophils due to different stimuli. Medicine-based inhibition of the over-activation of neutrophils or production and activity of elastase have been suggested to mend inflammatory diseases. Although the development of new elastase inhibitors is an essential strategy for treating the different inflammatory diseases, it has been a challenge to specifically target the activity of elastase because of its overlapping functions with those of other serine proteases. This review article highlights the reported natural polypeptides as potential inhibitors of elastase enzyme. The mechanism of action, structural features, and activity of the polypeptides have also been correlated wherever they were available.
人中性粒细胞弹性蛋白酶(HNE)是多种不同慢性和炎症性疾病中组织破坏的主要原因。弹性蛋白酶的过度表达在包括慢性阻塞性肺疾病(COPD)、急性呼吸窘迫综合征、类风湿性关节炎、罕见疾病周期性造血(或周期性中性粒细胞减少症)、感染、败血症、囊性纤维化、心肌缺血/再灌注损伤和哮喘、炎症以及动脉粥样硬化等各种疾病的发病机制中起重要作用。人中性粒细胞弹性蛋白酶由人中性粒细胞因不同刺激而分泌。基于药物抑制中性粒细胞过度活化或弹性蛋白酶的产生及活性已被建议用于改善炎症性疾病。尽管开发新的弹性蛋白酶抑制剂是治疗不同炎症性疾病的重要策略,但由于其与其他丝氨酸蛋白酶功能重叠,特异性靶向弹性蛋白酶的活性一直是一项挑战。这篇综述文章重点介绍了已报道的作为弹性蛋白酶潜在抑制剂的天然多肽。只要有相关信息,还对这些多肽的作用机制、结构特征和活性进行了关联。