Suppr超能文献

血红素加氧酶-1与一氧化碳:炎症和过敏领域中新兴的治疗靶点

Heme oxygenase-1 and carbon monoxide: emerging therapeutic targets in inflammation and allergy.

作者信息

Pae Hyun-Ock, Lee Yong C, Chung Hun-Taeg

机构信息

Department of Microbiology and Immunology, Wonkwang University School of Medicine, Iksan, Republic of Korea.

出版信息

Recent Pat Inflamm Allergy Drug Discov. 2008 Nov;2(3):159-65. doi: 10.2174/187221308786241929.

Abstract

Cumulative evidence suggests that the induction of the antioxidant/anti-inflammatory heme oxygenase (HO)-1 may play a protective role in allergic inflammation. HO-1 suppresses mast cell degranulation and cytokine synthesis. The up-regulation of the HO-1 pathway has a significant protective effect against airway inflammation, mucus hyper-secretion, and hyper-responsiveness in a model of allergic asthma. Moreover, HO-1 inhibits T cell-dependent skin inflammation and differentiation and function of antigen-presenting cells. The precise underlying mechanisms for HO-1-based protection against allergic inflammation are not yet completely understood, but appear to involve the protective effects of HO-1 by-products, such as carbon monoxide (CO), biliverdin/bilirubin and free iron. Among the HO-1 by-products, CO has been shown to mimic some protective actions of HO-1 in allergic inflammations. This article reviews the latest knowledge, recent patent and studies on the protective roles and mechanisms of HO-1/CO in inflammation and allergy.

摘要

越来越多的证据表明,诱导抗氧化/抗炎血红素加氧酶(HO)-1可能在过敏性炎症中发挥保护作用。HO-1可抑制肥大细胞脱颗粒和细胞因子合成。在过敏性哮喘模型中,HO-1途径的上调对气道炎症、黏液过度分泌和高反应性具有显著的保护作用。此外,HO-1可抑制T细胞依赖性皮肤炎症以及抗原呈递细胞的分化和功能。基于HO-1对过敏性炎症的保护的确切潜在机制尚未完全明确,但似乎涉及HO-1副产物的保护作用,如一氧化碳(CO)、胆绿素/胆红素和游离铁。在HO-1副产物中,CO已被证明在过敏性炎症中可模拟HO-1的一些保护作用。本文综述了关于HO-1/CO在炎症和过敏中的保护作用及机制的最新知识、近期专利和研究。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验