首页 | 本学科首页   官方微博 | 高级检索  
检索        

二陈汤加味对COPD急性期患者CC16,SP-D及HAT/HDAC的影响
引用本文:尚立芝,季书,谢文英,薛红莉,刘志勇,刘坦,张静,杜红妍,李进京,孙春阳,刘晓蕙,梁娟娟,张淼,王祎.二陈汤加味对COPD急性期患者CC16,SP-D及HAT/HDAC的影响[J].中国实验方剂学杂志,2017,23(10):163-170.
作者姓名:尚立芝  季书  谢文英  薛红莉  刘志勇  刘坦  张静  杜红妍  李进京  孙春阳  刘晓蕙  梁娟娟  张淼  王祎
作者单位:河南中医药大学 基础医学院, 郑州 450046,河南中医药大学 基础医学院, 郑州 450046,河南中医药大学 基础医学院, 郑州 450046,河南医学高等专科学校, 郑州 451191,河南中医药大学 第二附属医院, 郑州 450008,河南中医药大学 基础医学院, 郑州 450046,河南中医药大学 基础医学院, 郑州 450046,河南省人民医院, 郑州 450003,河南中医药大学 基础医学院, 郑州 450046,河南中医药大学 基础医学院, 郑州 450046,河南中医药大学 基础医学院, 郑州 450046,河南中医药大学 基础医学院, 郑州 450046,河南中医药大学 基础医学院, 郑州 450046,河南中医药大学 基础医学院, 郑州 450046
基金项目:国家自然科学基金面上项目(81573881);郑州市科技领军人才项目(121PLJRC535);河南省高等学校重点科研项目(15A360030);河南省重点科技攻关项目(152102310337);河南省中医药科学研究专项(2013ZY02070);河南中医药大学大学生创新学习项目(CXXM[2016]0019,CXXM[2016]0041)
摘    要:目的:观察二陈汤加味对COPD急性期加重期(acute exacerbation period of COPD,AECOPD)患者血浆、呼气冷凝液(exhale breath condensat,EBC)中克拉拉细胞蛋白(Clara cell protein,CC16),肺表面活性蛋白-D(pulmonary surfactant associated protein-D,SP-D)含量及外周血单个核细胞(peripheral blood mononuclear cell,PBMC)中组蛋白乙酰基转移酶(histone acetyl transferase,HAT)及组蛋白去乙酰基酶(histone deacetylase,HDAC)活性的影响,评价二陈汤加味对AECOPD的作用及机制。方法:选取符合纳入标准AECOPD患者200例,随机分成对照组和治疗组,每组100例。两组均在西医常规治疗的基础上,对照组给予安慰剂,治疗组接受二陈汤加味治疗,疗程14 d。检测肺功能,酶联免疫吸附试验(ELISA)法测定血浆,EBC中白细胞介素-17(interleukin-17,IL-17),C反应蛋白(C-reactive protein,CRP),CC16,SP-D及PBMC中HDAC1,HDAC2浓度。酶联免疫荧光法测定PBMC中HAT及HDAC活性。结果:与对照组治疗后比较,治疗组血浆及EBC中CRP,IL-17,CC16和SP-D水平均明显降低(P0.05,P0.01),PBMC中HAT活性明显降低(P0.05),HDAC活性,HDAC2含量均明显增高(P0.05)。结论:二陈汤加味可能调整HAT/HDAC的平衡,发挥抗炎作用,保护气道和肺的结构与功能。

关 键 词:慢性阻塞性肺疾病  二陈汤  克拉拉细胞蛋白  肺表面活性蛋白D  组蛋白乙酰基转移酶  组蛋白去乙酰基酶
收稿时间:2016/9/14 0:00:00

Effect of Modified Erchentang on CC16, SP-D and HAT and HDAC in Patients at Acute Exacerbation Stage of COPD
SHANG Li-zhi,JI Shu,XIE Wen-ying,XUE Hong-li,LIU Zhi-yong,LIU Tan,ZHANG Jing,DU Hong-yan,LI Jin-jing,SUN Chun-yang,LIU Xiao-hui,LIANG Juan-Juan,ZHANG Miao and WANG Yi.Effect of Modified Erchentang on CC16, SP-D and HAT and HDAC in Patients at Acute Exacerbation Stage of COPD[J].China Journal of Experimental Traditional Medical Formulae,2017,23(10):163-170.
Authors:SHANG Li-zhi  JI Shu  XIE Wen-ying  XUE Hong-li  LIU Zhi-yong  LIU Tan  ZHANG Jing  DU Hong-yan  LI Jin-jing  SUN Chun-yang  LIU Xiao-hui  LIANG Juan-Juan  ZHANG Miao and WANG Yi
Institution:School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China,School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China,School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China,Henan Medical College, Zhengzhou 451191, China,The Second Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou 450008, China,School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China,School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China,Henan Provincial People''s Hospital, Zhengzhou 450003, China,School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China,School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China,School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China,School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China,School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China and School of Basic Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China
Abstract:Objective: To study of the effect and mechanism of modified Erchentang on Clara cell protein (CC16), pulmonary surfactant associated protein-D (SP-D), histone acetyl transferase (HAT) and histone deacetylase (HDAC) in patients at acute aggravating stage of COPD. Method: Totally 200 cases at acute exacerbation period of COPD (AECOPD) were randomly divided into modified Erchentang group and placebo-controlled group, with 100 cases in each group. In addition to western drugs, modified Erchentang was also used in the modified Erchentang group, and placebo was also used in control group for 14 days. Their pulmonary function was detected, and euzyme-linked immunosorbent assay was used to determine the levels of C-reactive protein (CRP), interleukin-17 (IL-17), CC16, SP-D, HDAC1 and HAD2 in plasma and exhaled breath condensate of all groups. The activities of HAT and HDAC were determinate by enzyme-linked immune fluorescence. Result: The activity of HDAC2 was higher significantly, but the levels of CRP, IL-17, CC16 and SP-D (P<0.05, P<0.01) in plasma and exhaled breath condensate, and the activity of HAT were significantly decreased in treatment group with modified Erchentang, compared with those in control group. Conclusion: Modified Erchentang may have an effect on COPD by adjusting the HAT/HDAC, reducing levels of CRP, IL-17, CC16 and SP-D, preventing inflammation progress and improving the structure and function of respiratory system and lungs.
Keywords:chronic obstructive pulmonary disease (COPD)  Erchentang  Clara cell protein (CC16)  pulmonary surfactant associated protein-D(SP-D)  histone acetyl transferase (HAT)  histone deacetylase (HDAC)
本文献已被 CNKI 等数据库收录!
点击此处可从《中国实验方剂学杂志》浏览原始摘要信息
点击此处可从《中国实验方剂学杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号