首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effects of atrial natriuretic peptide and nitroprusside on isolated pulmonary resistance and conduit arteries from rats with pulmonary hypertension.
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Effects of atrial natriuretic peptide and nitroprusside on isolated pulmonary resistance and conduit arteries from rats with pulmonary hypertension.

机译:心钠素和硝普钠对肺动脉高压大鼠离体肺阻力和导管动脉的影响。

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摘要

1. The relaxant effects of atrial natriuretic peptide (ANP) and nitroprusside were studied on prostaglandin F2 alpha (PGF2 alpha)-contracted preparations of pulmonary resistance vessels (internal diameter 200-500 microns) and main pulmonary arteries taken from rats with pulmonary hypertension induced by monocrotaline (105 mg kg-1, s.c., 4 weeks previously). Control rats received saline. 2. In preparations from monocrotaline-treated rats, the potencies (negative log EC50) of ANP on resistance vessels (8.45) and main pulmonary arteries (8.25) were similar to those obtained in vessels from control rats (8.78 and 8.53 respectively), whereas those of nitroprusside were significantly less than in controls in both resistance vessels (7.13 compared with 7.63 in controls; three fold decrease in potency) and main pulmonary arteries (6.92 compared with 8.17 in controls; 18 fold decrease in potency). 3. On pulmonary resistance vessels from monocrotaline-treated rats, the maximum relaxant responses to ANP and nitroprusside, and also to pinacidil, were increased compared with controls, and reversal of the PGF2 alpha-induced contraction by these drugs was greater than 100%. In contrast, on main pulmonary arteries from monocrotaline-treated rats, the maximum relaxations to ANP and nitroprusside were not increased relative to controls, and reversal of PGF2 alpha was not greater than 100%.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.研究了心钠素和硝普钠对前列腺素F2α(PGF2α)收缩的肺阻力血管制剂(内径200-500微米)和肺动脉高压大鼠的主要肺动脉的舒张作用用吗啉(105 mg kg-1,sc,4周前)。对照大鼠接受盐水。 2.在用单crocrotaline处理的大鼠的制剂中,ANP对耐药性血管(8.45)和主要肺动脉(8.25)的效力(阴性对数EC50)与从对照大鼠的血管中产生的效力(分别为8.78和8.53)相似,而硝普钠的耐药性在两个阻力血管中均显着低于对照组(对照组为7.13,对照组为7.63;效能降低三倍)和主要肺动脉(对照组为6.92,与8.17相比;效能降低18倍)。 3.在用单crocrotaline处理的大鼠的肺阻力血管上,与对照组相比,对ANP和硝普钠以及对吡那地尔的最大舒张反应增加,并且这些药物逆转PGF2α诱导的收缩大于100%。相比之下,在单屈他啉处理的大鼠的主要肺动脉上,相对于对照组,ANP和硝普钠的最大舒张没有增加,并且PGF2α的逆转不大于100%。(摘要截断为250字)

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