您的位置:山东大学 -> 科技期刊社 -> 《山东大学学报(医学版)》

山东大学学报(医学版) ›› 2012, Vol. 50 ›› Issue (6): 65-.

• 基础医学 • 上一篇    下一篇

辛伐他汀对COPD大鼠肺组织凋亡相关因子的影响

丁启翠1,王伟1,王永彬1,陈旭东2,吴倩1   

  1. 1.山东大学第二医院呼吸科, 济南 250033; 2.山东省交通医院呼吸科, 济南 250031
  • 收稿日期:2011-11-22 出版日期:2012-06-10 发布日期:2012-06-10
  • 通讯作者: 王伟(1963- ),男,主任医师,硕导,主要从事慢性阻塞性肺疾病的诊断和治疗。 E-mail:ww8160@163.com
  • 作者简介:丁启翠(1985- ),女,硕士研究生,主要从事慢性阻塞性肺疾病的诊断和治疗
  • 基金资助:

    山东省自然科学基金资助项目(Y2008C19)

Effect of simvastatin on lung apoptotic factor in chronic
obstructive pulmonary disease rat models

DING Qi-cui1, WANG Wei1, WANG Yong-bin1, CHEN Xu-dong2, WU Qian1   

  1. 1. Department of Respiratory, The Second Hospital of Shandong University,Jinan 250033, China;
    2. Department of Respiratory, The Traffic Hospital of Shandong Province, Jinan 250031, China
  • Received:2011-11-22 Online:2012-06-10 Published:2012-06-10

摘要:

目的   探讨辛伐他汀对慢性阻塞性肺疾病(COPD)模型大鼠肺组织凋亡相关因子的影响及作用机制。方法   随机将30只大鼠分为正常组、对照组、治疗组。对照组采用熏香烟加气管内滴入LPS法建立大鼠COPD模型,香烟暴露2周后治疗组同时给予辛伐他汀(2.5mg/kg)治疗6周, 8周后处死所有大鼠,HE染色观察大鼠肺组织病理改变,显微图像分析系统计算肺平均内衬间隔和平均肺泡数,免疫组织化学技术检测大鼠肺组织半胱氨酸蛋白酶-3(Caspase-3)、诱导型一氧化氮合酶(iNOS)和内皮型一氧化氮合酶(eNOS)的水平。结果   对照组可见肺气肿和气道周围炎性改变,治疗组症状较对照组减轻;与正常组相比,对照组和治疗组肺平均内衬间隔(MLI)、iNOS、Caspase-3增多(P<0.05),平均肺泡数(MAN)、eNOS减少(P<0.05);与对照组比较,治疗组MLI、iNOS、Caspase-3减少(P<0.05),MAN、eNOS增多(P<0.05)。各组大鼠肺组织中Caspase-3与iNOS呈正相关(P<0.05),与eNOS呈负相关(P<0.05)。结论   辛伐他汀通过增加肺组织eNOS表达,降低iNOS及Caspase-3表达,减少COPD肺组织细胞凋亡,在COPD中起到保护性作用。

关键词: 肺疾病,慢性阻塞性;细胞凋亡;辛伐他汀;大鼠

Abstract:

Objective   To determine the effect and mechanism of simvastatin on lung apoptotic factors in chronic obstructive pulmonary disease(COPD)rat models. Methods   30 rats were randomly divided into three groups: the normal group, the control group and the treatment group. The control group was treated by being exposed to smoking and intratracheal instillation of lipopolysaccharide to establish the COPD rat models. 2 weeks later, the treatment group was treated with 2.5mg/kg simvastatin daily for 6 weeks. The rats were executed after 8 weeks. Lung tissue sections stained by hematoxylin and eosin (HE) were observed, and mean linear intercept as well as mean alveolar numbers were measured by micrographical analysis. Expressions of eNOS, iNOS and caspase-3 were measured by immunohistochemistry. Results   Emphysema and airway inflammation were observed in the control group, and the symptoms of the treatment group were lighter. Compared with the normal group, the mean linear intercept(MLI), iNOS, Caspase-3 in the control and treatment groups increased(P<0.05), and the mean alveolar numbers (MAN) and eNOS decreased(P<0.05). Compared with the control group, the MLI, iNOS, Caspase-3 decreased(P<0.05) and the MAN and eNOS increased(P<0.05) in the treatment group. Caspase-3 in the lung tissue of each group positively correlated with iNOS(P<0.05), and negatively with eNOS(P<0.05). Conclusion   Simvastatin has a protective effect on the COPD rat models by increasing expression of eNOS and decreasing the expressions of iNOS and Caspase-3 which can reduce the apoptosis of COPD lung tissue.

Key words: Pulmonary disease, chronic obstructive; Apoptosis; Simvastatin; Rats

中图分类号: 

  • R563.3
[1] 陈旭东,王伟,王永彬. 辛伐他汀对COPD大鼠模型炎症的干预作用[J]. 山东大学学报(医学版), 2010, 48(4): 36-.
[2] . SERPINE2基因多态性与慢性阻塞性肺疾病的相关性[J]. 山东大学学报(医学版), 2009, 47(7): 111-114.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!