我们的网站为什么显示成这样?

可能因为您的浏览器不支持样式,您可以更新您的浏览器到最新版本,以获取对此功能的支持,访问下面的网站,获取关于浏览器的信息:

|本期目录/Table of Contents|

波生坦对慢性低氧性肺动脉高压大鼠右心室肥厚及缝隙连接蛋白(Cx)43表达的影响

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2010年第1期
页码:
51-55
栏目:
基础研究
出版日期:
2010-01-04

文章信息/Info

Title:
Effects of bosentan on right ventricular hypertrophy and connexin43 in rats with chronic hypoxic pulmonary hypertension
作者:
刘海莲1张玉顺2王佳兴1朱妙章3
第四军医大学:1.西京医院心内科, 3.生理学教研室, 陕西 西安 710032; 2.西安交通大学医学院第一附属医院心内二科, 陕西 西安 710061
Author(s):
LIU Hai-lian1 ZHANG Yu-shun2 WANG Jia-xing1 ZHU Miao-zhang3
1.Department of Cardiology, Xijing Hospital, Fourth Military Medical University, Xi’an 710032, Shaanxi, China; 2.Second Department of Cardiology, First Affiliated Hospital, Medical School of Xi’an Jiaotong University, Xi’an 710061, Shaanxi, China; 3.Depar
关键词:
低氧性肺动脉高压波生坦心肌肥厚缝隙连接蛋白Cx43大鼠
Keywords:
hypoxic pulmonary hypertension bosentan hypertrophy connexin43 rats
分类号:
R541.3
DOI:
-
文献标识码:
A
摘要:
目的: 研究波生坦(bosentan,BST)对慢性低压低氧性肺动脉高压(HPH)大鼠右心室肥厚及缝隙连接蛋白43(Cx43)表达量的影响。方法: 将24只实验动物随机分为正常组、HPH组、安慰剂组和BST治疗组,每组各6只。正常组:常压常氧下饲养6周;其他3组大鼠置于低压低氧仓内8 h/d,共6周,从第4周开始,每天给BST治疗组大鼠BST (100 mg/kg)灌胃,安慰剂组生理盐水灌胃。6周后,所有大鼠测定血流动力学指标:如平均肺动脉压力(mPAP)、右心室收缩压(RVSP)、右心室收缩压上升最大速率(dp/dtmax),以及右心室肥厚度[如右心室质量/(左心室质量+室间隔质量),RV/(LV+S)]和右心室质量/体质量(RW/BW)。收集动脉血检测血浆内皮素-1(ET-1)和一氧化氮(NO)水平。Masson染色观察心肌胶原纤维容积百分比的变化,免疫组化染色法和Western blot观察Cx43的变化。结果: BST治疗组大鼠的mPAP、RVSP、RV/(LV+S)、RW/BW及心肌胶原纤维容积百分比均较HPH组显著降低(P<0.05),但血浆NO、ET-1的水平和心肌Cx43表达量显著升高(P<0.05)。结论: BST在降低肺动脉压力的同时,还可抑制右心室肥厚和Cx43表达量的降低。
Abstract:
AIM: To study the effects of bosentan on right ventricular hypertrophy and connexin43 in rats with chronic hypoxic pulmonary hypertension (HPH). METHODS: Twenty four rats were randomly divided into four groups: control group, bosentan group, placebo group and HPH group. Rats in the control group were in a normal environment for 6 weeks. Rats in the other groups were kept in a hypobaric chamber that simulated the 5 000 m altitude for 8 h/day for 6 weeks. For placebo group and bosentan group, sodium chloride or bosentan was given for 3 weeks starting from the fourth week. At the end of the 6 weeks, pulmonary arterial pressure (PAP) and right ventricular systolic pressure (RVSP) were determined, RV/LV+S and the weight ratio of the right ventricle weight vs. body weight (RW/BW) were calculated. Right ventricle tissues were Masson stained to observe the degree of myocardial fibrosis. Expression of connexin43 was detected by immunohistochemistry and Western blot. Levels of NO and ET-1 in plasma were measured. RESULTS: PAP and RVSP significantly decreased in bosentan group compared with HPH group (P<0.05). The development of the RV/LV+S and RW/BW was significantly prevented in the bosentan group. Masson stain showed that the degree of myocardial fibrosis significantly decreased in bosentan group compared with HPH group (P<0.05). Level of ET-1 and NO in plasma significantly increased in bosentan group compared with that in HPH group (P<0.05). Expression of connexin43 significantly increased in the bosentan group compared with HPH group (P<0.05). CONCLUSION: Bosentan effectively decreases pulmonary artery pressure and restrains right ventricular hypertrophy and remodeling of connexin43.

参考文献/References

[1] Benza RL, Rayburn BK, Tallaj JA, et al. Efficacy of bosentan in a small cohort of adult patients with pulmonary arterial hypertension related to congenital heart disease[J]. Chest Apr, 2006, 129(4):1009-10015.

[2] 李娟,孙新,毕辉,等. 低压低氧性大鼠肺动脉高压模型的建立[J]. 临床心血管病杂志, 2008, 24(4):297-301.

[3] Roux S, Breu V, Ertel SI, et al. Endothelin antagonism with bosentan: a review of potential applications[J]. J Mol Med, 1999, 77(4):364-376.

[4] Pei JM, Sun X, Guo HT, et al. U50,488H Depresses pulmonary pressure in rats subjected to chronic hypoxia[J]. J Cardiovasc Pharmacol, 2006, 47(4):594-598.

[5] Jessup M. Brozena S. Heart Failure[J]. N Engl J Med, 2003, 348(20):2007-2018.

[6] 陈莉延,麦奇,彭勃,等. 白藜芦醇苷对慢性常压低氧性PH模型中磷脂酶A-2、一氧化氮和内皮素水平的影响[J]. 中国病理生理杂志, 2006, 22(5):953-955.

[7] Lee SH, Channick RN. Endothelin antagonism in pulmonary arterial hypertension[J]. Semin Respir Crit Care Med, 2005, 26(4):402-408.

[8] 任安经,袁文俊. 心肌细胞内皮素的信号传导[J]. 中国医学科学院学报, 2005, 27(4):529-533.

[9] 油红文,陈曦,刘国仗.内皮素对心脏细胞DNA和蛋白合成的作用[J]. 高血压杂志, 2004, 12(2):161-164.

[10]荆志成. 波生坦治疗肺动脉高压的药理机制及其临床评价[J]. 中国医院用药评价与分析, 2005, 15(6):334-338.

[11]殷召,张权宇,王跃民,等. 连接蛋白43表达的变化与心律失常的关系[J]. 心脏杂志, 2008, 20(2):244-247.

[12]Kostin S, Dammer S, Hein S, et al. Connexin 43 expression and distribution in compensated and decompensated cardiac hypertrophy in patients with aortic stenosis[J]. Cardiovasc Res, 2004, 62(2):426-436.

[13]Rudy Y, Shaw RM. Cardiac exitation: an interactive process of ion channels and gap junctions[J]. Adv Exp Med Biol, 1997, 430:269-279.

[14]Shi-Wen X, Denton CP, Dashwood MR, et al. Fibroblast matrix gene expression and connective tissue remodeling: role of endothelin-1[J]. J Invest Dermatol, 2001, 103(2):753-758.

[15]Weber C, Schmitt R, Birnboeck H, et al .Pharmacokinetics and pharmacodynamics of the endothelin-receptor antagonist bosentan in healthy human subjects[J]. Clin Pharmacol Ther, 1996, 60(2):124-137.

[16]Teunissen BE, Jongsma HJ, Bierhuizen MF. Regulation of myocardial connexins during hypertrophic remodeling[J]. Eur Heart J, 2004, 25(22):1979-1989.

[17]Jozsef L, Khreiss T, Fournier A, et al. Extracellular signal-regulated kinase plays an essential role in endothelin-1-induced homotypic adhesion of human neutrophil granulocytes[J]. Br J Pharmacol, 2002, 135(5):1167-1174.

备注/Memo

备注/Memo:
收稿日期:2009-1-15.通讯作者:张玉顺,教授,主要从事先天性心脏病的介入治疗的研究Email:zys2889@sina.com 作者简介:刘海莲,硕士生Email:liuhailian79@163.com
更新日期/Last Update: 2010-01-05