前列环素(PGI2)和7-氧-PGI2对离体脑动脉、冠状动脉和肠系膜动脉的松弛作用。

B Malomvölgyi, P Hadházy, K Magyar, K Kánai, V Simonidesz
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引用次数: 0

摘要

本研究比较了华宁制药厂产品前列环素(PGI2)及其稳定的7-氧类似物对犬离体脑、牛冠状动脉、兔腹腔和人肠系膜动脉条带的松弛作用。两种前列腺素均可降低冠状动脉、大脑动脉和人肠系膜动脉的静息张力,以及刺激或去甲肾上腺素诱发的腹腔血管张力。7-oxo-PGI2的松弛作用起效缓慢,并持续到被冲掉。PGI2的IC50为4 ~ 40 × 10(-9) mol/l, 7-oxo-PGI2的IC50为1 ~ 6 × 10(-7) mol/l。与PGI2相比,7-oxo-PGI2在冠状动脉舒张中的作用比其他血管更强。PGI2使离体豚鼠气管收缩,7-oxo-PGI2使气管松弛。
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Relaxation by prostacyclin (PGI2) and 7-oxo-PGI2 of isolated cerebral, coronary and mesenteric arteries.

The relaxant effects of prostacyclin (PGI2) and its stable 7-oxo-analogue, a product of Chinoin Pharmaceutical Works, were compared on isolated canine cerebral, bovine coronary, rabbit coeliac and human mesenteric arterial strips. The resting tone of the coronary, cerebral and human mesenteric arteries as well as the stimulation- or noradrenaline-evoked tone of coeliac vessels were reduced by both prostanoids. The relaxant action of 7-oxo-PGI2 was slow in onset and lasted until it was washed out. The IC50 values were 4 to 40 X 10(-9) mol/l for PGI2 and 1 to 6 X 10(-7) mol/L for 7-oxo-PGI2. Compared to PGI2, 7-oxo-PGI2 was more potent in relaxing coronary arteries than the other vessels studied. Isolated tracheae from guinea-pigs were contracted by PGI2 while relaxed by 7-oxo-PGI2.

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