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

    Effects of bosentan on right ventricular hypertrophy and connexin43 in rats with chronic hypoxic pulmonary hypertension

    • 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.

       

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