首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Reduced relaxant potency of nitroprusside on pulmonary artery preparations taken from rats during the development of hypoxic pulmonary hypertension.
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Reduced relaxant potency of nitroprusside on pulmonary artery preparations taken from rats during the development of hypoxic pulmonary hypertension.

机译:缺氧性肺动脉高压发展过程中硝普钠对大鼠肺动脉制剂的松弛作用降低。

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摘要

1. Relaxant responses to nitroprusside were examined on U46619-contracted pulmonary artery ring preparations from rats exposed to hypoxia, in chambers containing 10% oxygen, for 1, 3, or 14 days, or for 14 days followed by 12 days in room air. Control rats were housed in room air. 2. After 3 days of hypoxia (but not 1 day), rats had elevated pulmonary artery pressure, right ventricular hypertrophy and polycythemia. After 14 days of hypoxia there was, in addition, hypertrophy of the pulmonary artery. In rats returned to room air for 12 days after 14 days of hypoxia, there was still some right ventricular and vascular hypertrophy but no increase in pulmonary artery pressure or polycythemia. 3. The potency (neg log EC50) of nitroprusside on pulmonary arteries taken from rats after 3 or 14 days of hypoxia was significantly less than on preparations from control rats (3 and 11 fold, respectively). This was not seen after 1 day of hypoxia or after 14 days of hypoxia followed by 12 days in room air. Removal of the endothelium from the preparations had no effect on the potency of nitroprusside in control or hypoxic rats (14 days). 4. In preparations from hypoxic, but not control, rats (14 days), the maximum response to nitroprusside was > 100% (177% reversal of the U46619 contraction) in the absence, but not in the presence, of the endothelium, indicating that pulmonary arteries from hypoxic rats had inherent tone which could be counteracted by a relaxing factor from the endothelium. 5. Exposure of rats to hypoxia (14 days) did not affect the potency of nitroprusside on aorta or trachea.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.在暴露于低氧的大鼠的U46619收缩的肺动脉环制剂中,在含10%氧的室内进行1、3或14天或14天,然后在室内空气中放置12天,然后检查其对硝普钠的松弛反应。将对照大鼠饲养在室内空气中。 2.缺氧3天(但不是1天)后,大鼠的肺动脉压升高,右心室肥大和红细胞增多症。缺氧14天后,肺动脉肥大。在缺氧14天后恢复室内空气12天的大鼠中,右心室和血管肥大仍然存在,但肺动脉压力或红细胞增多症没有增加。 3.硝普钠在缺氧3天或14天后对大鼠肺动脉的效力(neg log EC50)显着低于对照大鼠制剂(分别为3倍和11倍)。在缺氧1天后或在缺氧14天后再在室内空气中放置12天后,未见此现象。从制品中去除内皮对对照组或低氧大鼠(14天)中硝普钠的效力没有影响。 4.在缺氧但非对照大鼠的制剂中(14天),在没有(但没有)内皮存在的情况下,对硝普钠的最大反应> 100%(U46619收缩的反向177%),表明缺氧大鼠的肺动脉具有固有的张力,可以被内皮的松弛因子所抵消。 5.大鼠缺氧(14天)不会影响硝普钠对主动脉或气管的效力。(摘要截短为250字)

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