• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

不同治疗策略对哮喘和慢性阻塞性肺疾病患者呼出气一氧化氮及肺部炎症的影响

Influence of different therapeutic strategies on exhaled NO and lung inflammation in asthma and COPD.

作者信息

Kharitonov Sergei A

机构信息

Section of Airway Disease, National Heart and Lung Institute, Imperial College and Royal Brompton and Harefield NHS Trust, London SW3 6LY, UK.

出版信息

Vascul Pharmacol. 2005 Dec;43(6):371-8. doi: 10.1016/j.vph.2005.08.002. Epub 2005 Sep 28.

DOI:10.1016/j.vph.2005.08.002
PMID:16198155
Abstract

Nitric oxide (NO), a simple free radical gas, elicits a diverse range of physiological and pathophysiological effects, and plays an important role in pulmonary diseases. Nitrosative stress and nitration of proteins in airway epithelium maybe responsible for steroid resistance in asthma and their ineffectiveness in chronic obstructive pulmonary disease (COPD), supporting the potential role of future therapeutic strategies aimed at regulating NO synthesis in asthma and COPD. Here, we have reviewed the potential role of NO modulators (NO synthase inhibitors and NO donors), which if given on a regular basis may have clinical benefit in asthma and COPD.

摘要

一氧化氮(NO)是一种简单的自由基气体,可引发多种生理和病理生理效应,在肺部疾病中起重要作用。气道上皮中的亚硝化应激和蛋白质硝化可能是哮喘中类固醇抵抗及其在慢性阻塞性肺疾病(COPD)中无效的原因,这支持了未来旨在调节哮喘和COPD中NO合成的治疗策略的潜在作用。在此,我们综述了NO调节剂(NO合酶抑制剂和NO供体)的潜在作用,定期给予这些调节剂可能对哮喘和COPD具有临床益处。

相似文献

1
Influence of different therapeutic strategies on exhaled NO and lung inflammation in asthma and COPD.不同治疗策略对哮喘和慢性阻塞性肺疾病患者呼出气一氧化氮及肺部炎症的影响
Vascul Pharmacol. 2005 Dec;43(6):371-8. doi: 10.1016/j.vph.2005.08.002. Epub 2005 Sep 28.
2
Modulation of nitric oxide pathways: therapeutic potential in asthma and chronic obstructive pulmonary disease.一氧化氮途径的调节:在哮喘和慢性阻塞性肺疾病中的治疗潜力
Eur J Pharmacol. 2006 Mar 8;533(1-3):263-76. doi: 10.1016/j.ejphar.2005.12.069. Epub 2006 Feb 7.
3
Nitric oxide, nitrotyrosine, and nitric oxide modulators in asthma and chronic obstructive pulmonary disease.
Curr Allergy Asthma Rep. 2003 Mar;3(2):121-9. doi: 10.1007/s11882-003-0024-7.
4
NOS:molecular mechanisms, clinical aspects, therapeutic and monitoring approaches.一氧化氮合酶:分子机制、临床方面、治疗与监测方法。
Curr Drug Targets Inflamm Allergy. 2005 Apr;4(2):141-9. doi: 10.2174/1568010053586282.
5
[Endogenous nitric oxide in obstructive pulmonary diseases].
Wiad Lek. 2005;58(3-4):238-42.
6
Differences of inflammatory mechanisms in asthma and COPD.哮喘和 COPD 中炎症机制的差异。
Allergol Int. 2009 Sep;58(3):307-13. doi: 10.2332/allergolint.09-RAI-0106. Epub 2009 Jul 25.
7
Defining the role of exhaled nitric oxide measurements in COPD.确定呼出一氧化氮测量在慢性阻塞性肺疾病中的作用。
Respirology. 2010 Apr;15(3):385-6. doi: 10.1111/j.1440-1843.2010.01730.x.
8
[Exhaled nitric oxide (NO) in patients with respiratory tract diseases].[呼吸道疾病患者呼出的一氧化氮(NO)]
Pol Merkur Lekarski. 2004 Feb;16(92):115-8.
9
Airway nitrergic pathways: is there therapeutic potential in asthma and COPD?气道一氧化氮能通路:在哮喘和慢性阻塞性肺疾病中是否具有治疗潜力?
Curr Opin Pharmacol. 2004 Jun;4(3):202-6. doi: 10.1016/j.coph.2004.01.005.
10
The small airways and distal lung compartment in asthma and COPD: a time for reappraisal.哮喘和 COPD 中的小气道和远端肺区:重新评估的时候到了。
Allergy. 2010 Feb;65(2):141-51. doi: 10.1111/j.1398-9995.2009.02242.x. Epub 2009 Nov 11.

引用本文的文献

1
Nitric Oxide Metabolites and Lung Cancer Incidence: A Matched Case-Control Study Nested in the ESTHER Cohort.一氧化氮代谢物与肺癌发病率:嵌套在 ESTHER 队列中的匹配病例对照研究。
Oxid Med Cell Longev. 2019 Sep 2;2019:6470950. doi: 10.1155/2019/6470950. eCollection 2019.
2
Repeated lipopolysaccharide exposure causes corticosteroid insensitive airway inflammation via activation of phosphoinositide-3-kinase δ pathway.反复暴露于脂多糖通过磷酸肌醇-3-激酶δ途径的激活导致皮质类固醇不敏感的气道炎症。
Biochem Biophys Rep. 2016 Jul 28;7:367-373. doi: 10.1016/j.bbrep.2016.07.020. eCollection 2016 Sep.