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进一步的证据表明,细胞色素P-450介导的反应与羔羊动脉导管的收缩张力有关。

Further evidence implicating a cytochrome P-450-mediated reaction in the contractile tension of the lamb ductus arteriosus.

作者信息

Coceani F, Breen C A, Lees J G, Falck J R, Olley P M

机构信息

Research Institute, Hospital for Sick Children, Toronto, Canada.

出版信息

Circ Res. 1988 Mar;62(3):471-7. doi: 10.1161/01.res.62.3.471.

DOI:10.1161/01.res.62.3.471
PMID:3124973
Abstract

The authors have recently provided evidence implicating the cytochrome P-450 system in the generation of contractile tension of the ductus arteriosus. To confirm this possibility, carbon monoxide (CO/O2 ratio, 0.27) and cytochrome P-450 inhibitors [4-phenylimidazole; 14-isocyano,15-(methoxymethyleneoxy)-5Z,8Z,11 Z-eicosatrienoic acid; 9-hydroxyellipticine; alpha-naphthoflavone] were tested on the isolated ductus arteriosus from mature fetal lambs equilibrated at low (4-26 mm Hg) or high (229-694 mm Hg) O2 partial pressure (PO2). Carbon monoxide completely relaxed intact vessel wall preparations and preparations consisting of only the muscle. Carbon monoxide relaxation was reversed by illumination with monochromatic light and the peak for the photoactivated contraction occurred at 450 nm. 4-Phenylimidazole (100 and 1,000 microM) was also a relaxant agent, and its action was manifest at both low and high PO2. Unlike 4-phenylimidazole, the isonitrile compound (5 microM) and 9-hydroxyellipticine (10 and 100 microM) were relaxant only at low PO2 and were also less potent. At the same PO2, alpha-naphthoflavone (10 microM) barely reduced ductal tension. Treatment of the ductus with either a combination of superoxide dismutase (60 or 150 U/ml) and catalase (40 or 1,000 U/ml) or mannitol alone (80 mM) failed to alter the steady-state tone at low PO2 and the contractile response to O2. Arachidonic acid was tested on tissues pretreated with the dual cyclooxygenase and lipoxygenase inhibitor, BW755C (10 microM), and produced a weak relaxation at a concentration of 1 microM or higher. 5,6-Epoxytrienoic acid relaxed the untreated tissue, and its action was abolished by indomethacin (2.8 microM).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

作者最近提供了证据,表明细胞色素P - 450系统与动脉导管收缩张力的产生有关。为证实这一可能性,对来自成熟胎羊的离体动脉导管进行了一氧化碳(CO/O₂ 比率为0.27)和细胞色素P - 450抑制剂[4 - 苯基咪唑;14 - 异氰基,15 - (甲氧基亚甲基氧基)- 5Z,8Z,11Z - 二十碳三烯酸;9 - 羟基玫瑰树碱;α - 萘黄酮]的测试,这些胎羊的动脉导管在低(4 - 26 mmHg)或高(229 - 694 mmHg)氧分压(PO₂)下达到平衡。一氧化碳使完整的血管壁制剂和仅由肌肉组成的制剂完全松弛。一氧化碳引起的松弛可被单色光照射逆转,光激活收缩的峰值出现在450 nm处。4 - 苯基咪唑(100和1000 μM)也是一种松弛剂,其作用在低和高PO₂ 时均有体现。与4 - 苯基咪唑不同,异腈化合物(5 μM)和9 - 羟基玫瑰树碱(10和100 μM)仅在低PO₂ 时起松弛作用,且效力较弱。在相同的PO₂ 下,α - 萘黄酮(10 μM)几乎不降低导管张力。用超氧化物歧化酶(60或150 U/ml)和过氧化氢酶(40或1000 U/ml)的组合或单独使用甘露醇(80 mM)处理动脉导管,未能改变低PO₂ 时的稳态张力以及对O₂ 的收缩反应。在预先用双环氧化酶和脂氧合酶抑制剂BW755C(10 μM)处理的组织上测试花生四烯酸,其在浓度为1 μM或更高时产生微弱的松弛作用。5,6 - 环氧三烯酸使未处理的组织松弛,其作用被吲哚美辛(2.8 μM)消除。(摘要截短于250字)

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