设为首页
加入收藏
联系我们
Email-Alert
 

    首页 | 杂志介绍 | 编委成员 | 投稿指南 | 订阅指南 | 过刊浏览 | 论著模板 | 综述模板 | 出版伦理声明 | 帮助

 
孙维梁,郭 静,张雨婷,曲木诗玮.康复运动通过调节大鼠肺脏NADPH氧化酶延缓慢性阻塞性肺疾病进程的研究[J].中国康复医学杂志,2025,(4):495~500
康复运动通过调节大鼠肺脏NADPH氧化酶延缓慢性阻塞性肺疾病进程的研究    点此下载全文
孙维梁  郭 静  张雨婷  曲木诗玮
中日友好医院临床医学研究所,北京市,100029
基金项目:国家自然科学基金青年项目(82200051)
DOI:10.3969/j.issn.1001-1242.2025.04.003
摘要点击次数: 89
全文下载次数: 52
摘要:
      摘要 目的:探讨NADPH氧化酶(NADPH oxidase,Nox)分子亚型在康复运动改善慢性阻塞性肺疾病(chronic obstructive pulmonary disease,COPD)中的表达及机制。 方法:将大鼠随机分为对照组、COPD组、COPD中等强度运动组和COPD较大强度运动组,每组10只。免疫组化检测缺氧诱导因子1α(hypoxia inducible factor-1α,HIF1α)、NADPH氧化酶分子、炎症因子——肿瘤坏死因子α(factors tumor necrosis factor alpha,TNFα)、白细胞介素-6(interleukin-6,IL-6)、基质金属蛋白酶2(matrix metalloproteinase 2,MMP-2)和基质金属蛋白酶9(matrix metalloproteinase 9,MMP-9)的表达。 结果:与对照组相比,COPD组NADPH氧化酶亚型Nox1、Nox2、Nox5、HIF1α、TNFα、IL-6、MMP-2和MMP-9表达明显增加,中等强度运动可以减少COPD动物模型Nox2、Nox5、MMP-9、HIF1α表达,较大强度运动可以减少Nox1、Nox2、Nox5、TNFα、IL-6、MMP-9、HIF1α表达。 结论:康复运动下调肺脏NADPH氧化酶不同亚型分子表达,进而减少下游炎症因子、TNFα、IL-6、MMP-2和MMP-9的表达,康复运动的保护功能可能通过抑制HIF1α的表达而实现。
关键词:慢性阻塞性肺疾病  NADPH氧化酶  缺氧诱导因子  炎症因子  基质金属蛋白酶
A study on rehabilitation exercise delaying the progression of chronic obstructive pulmonary disease by regulating NADPH oxidase in lung    Download Fulltext
China-Japan Friendship Hospital, Beijing, 100029
Fund Project:
Abstract:
      Abstract Objective:To investigate the expression of NADPH oxidase(Nox) in chronic obstructive pulmonary disease(COPD). Method: The rats were randomly divided into control group,COPD group,COPD medium exercise group and COPD intensive exercise group,with 10 rats in each group. The expression of NADPH oxidase, hypoxia inducible factor-1 alpha (HIF1α),inflammatory factors tumor necrosis——factor alpha(TNFα),interleukin-6(IL-6),matrix metalloproteinase 2(MMP-2) and matrix metalloproteinase 9(MMP-9) were detected by immunohistochemistry. Result: Compared with the control group, the expression of NADPH oxidase subtypes Nox1,Nox2,Nox5,HIF1α,TNFα,IL-6,MMP-2 and MMP-9 in COPD group increased significantly. Medium exercise reduced the expression of Nox2,Nox5, HIF1α and MMP-9 in COPD animal model, while intensive exercise reduced the expression of Nox1,Nox2,Nox5,HIF1α,TNFα,IL-6 and MMP-9. Conclusion: Rehabilitation exercise down regulated the expression of NADPH oxidases in lung, reduced the expression of downstream inflammatory factors and matrix metalloproteinase. The protective function of rehabilitation exercise might achieve by inhibiting the expression of hypoxia inducible factor.
Keywords:chronic obstructive pulmonary disease  NADPH oxidase  hypoxia inducible factor  matrix metalloproteinase
查看全文  查看/发表评论

您是本站第 40976833 位访问者

版权所有:中国康复医学会
主管单位:中国科学技术协会 主办单位:中国康复医学会
地址:北京市朝阳区樱花园东街,中日友好医院内   邮政编码:100029   电话:010-64218095   

本系统由北京勤云科技发展有限公司设计
京ICP备18060696号-2

京公网安备 11010502038612号