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姜黄素防治慢性低O2高CO2大鼠肺动脉高压与c-Jun、c-Fos的关系研究
引用本文:林全,王良兴,周向锋,黄晓颖,陈少贤. 姜黄素防治慢性低O2高CO2大鼠肺动脉高压与c-Jun、c-Fos的关系研究[J]. 中国临床药理学与治疗学, 2005, 10(10): 1118-1122
作者姓名:林全  王良兴  周向锋  黄晓颖  陈少贤
作者单位:1. 温州医学院附属一院呼吸科,温州,325003,浙江
2. 浙江金华职业技术学院医学院,金华,321017,浙江
基金项目:国家自然科学基金资助项目(№30472269)
摘    要:目的:研究姜黄素对慢性低O2高CO2大鼠肺动脉高压及肺动脉管壁c-Jun和c-Fos表达的影响.方法:36只SD大鼠随机分为正常对照组、低O2高CO2组、低O2高CO2+姜黄素组(简称姜黄组).采用图像分析、免疫组化和组织原位杂交技术等方法观察姜黄素对慢性低O2高CO2大鼠肺动脉压力、血管显微结构及肺动脉管壁原癌基因c-Jun和c-Fos表达影响.结果:血流动力学检测显示姜黄素组mPAP较低O2高CO2组明显降低(P<0.01),组间mCAP比较差异无显著性.光镜下姜黄素组肺细小动脉内弹力板扭曲、中膜平滑肌细胞增生及管腔狭窄程度均明显轻于低O2高CO2组.电镜下姜黄素组大鼠肺细小动脉内皮细胞结构基本正常,中膜平滑肌细胞增生较轻,胶原少见;外膜胶原纤维较低O2高CO2大鼠明显减少.免疫组化法发现肺细小动脉c-Jun和c-Fos平均吸光度值低O2高CO2组明显高于正常对照组(P<0.01),姜黄素组明显低于低O2高CO2组(P<0.01);原位杂交法显示肺细小动脉管壁c-Jun mRNA平均吸光度值姜黄素组显著低于低O2高CO2 组(P<0.01).结论:姜黄素有抑制慢性低O2高CO2性肺动脉高压和改善肺血管结构重建的作用,下调c-Fos、c-Jun及其基因的表达,抑制血管平滑肌细胞的增殖可能是其重要作用机制.

关 键 词:姜黄素 低氧 慢性 高碳酸血 高血压 肺性 转录激活蛋白-1
文章编号:1009-2501(2005)10-1118-04
收稿时间:2005-08-27
修稿时间:2005-09-27

Effect of curcumin on pulmonary arterial pressure and c-Jun,c-Fos in chronic hypoxic hypercapnic rats
LIN Quan,WANG Liang-xing,ZHOU Xiang-feng,HUANG Xiao-ying,CHEN Shao-xian. Effect of curcumin on pulmonary arterial pressure and c-Jun,c-Fos in chronic hypoxic hypercapnic rats[J]. Chinese Journal of Clinical Pharmacology and Therapeutics, 2005, 10(10): 1118-1122
Authors:LIN Quan  WANG Liang-xing  ZHOU Xiang-feng  HUANG Xiao-ying  CHEN Shao-xian
Affiliation:1.Department of Respirology First Hospital, Wenzhou Medical College Wenzhou 325003, Zhejiang , China ;2.Zhejting Jinhua Vocational Technical School, Jinhua 321000, Zhejiang, China
Abstract:AIM: To investigate the effect of curcumin on pulmonaiy arterial pressure and the expression of c-Jun and c-Fos in chronic hypoxia hypercapnia rats. METHODS: SD rats were randomly divided into normal control group (NC), hypoxic hypercapnic group (HH), hypoxic hypercapnia + curcumin group (HC). c-Fos, c-Jun and their mRNA were observed in pulmonary arterioles of rats by the technique of immunohistochemistry and in situ hybridization. RESULTS: Hemodynamics showed that mPAP was markedly lower in group HC than that in group HH (P<0.01). Differences of mCAP were not significant in three groups. Light microscopy showed media thickness of pulmonary arterioles was markedly higher in group HH than that in group NC, and vessel cavity turned more strait in group HH than that in group NC. However, the damage of pulmonary arterioles in group HC was significantly slighter than that of group HH. Electron microscopy showed that structure of the en- dothelial cells in pulmonary arterioles in group HC was near to normal, and the proliferation of medial smooth muscle cells and collagen fibers in adventitia is markedly lighter than those of group HH. Expression of c-Jun and c-Fos in pulmonary arterioles were significantly higher in group HH than those of NC group (P<0.01), and they were lower in group HC than those of group HH (P<0.01). In situ hybridization showed that c-Jun mRNA in pulmonary arterioles was significantly lower in rats of group HC than that in group HH. CONCLUSION: Curcumin can inhibit hypoxic hypercapnic pulmonary hypertension and pulmonary vessel remodeling, and it may be a vital mechanism of curcumin to decrease the expression of c-Jun, c-Fos and to inhibit the proliferation of medial smooth muscle cells.
Keywords:curcumin   hypoxia, chronic   hypercapnia   hypertension, pulmonary   activator protein-1
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