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羔羊静脉导管:其收缩张力中细胞色素P - 450机制的证据。

Lamb ductus venosus: evidence of a cytochrome P-450 mechanism in its contractile tension.

作者信息

Adeagbo A S, Breen C A, Cutz E, Lees J G, Olley P M, Coceani F

机构信息

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

出版信息

J Pharmacol Exp Ther. 1990 Feb;252(2):875-9.

PMID:2313604
Abstract

We have recently shown that a cytochrome P-450-based mechanism is important for the generation of contractile tension by the ductus arteriosus and have now examined whether the same mechanism operates in the ductus venosus. Carbon monoxide (CO/O2 ratio, 0.27) and cytochrome P-450 inhibitors [metyrapone; 4-phenylimidazole; 14-isocyano, 15-(methoxymethyleneoxy)-5Z,8Z,11Z- eicosatrienoic acid; alpha-naphthoflavone] were tested in vitro on the ductus venosus sphincter from mature fetal lambs. Each preparation was precontracted with indomethacin (2.8 x 10(-6) M). Carbon monoxide completely relaxed the ductus, and its action was reversed by illumination with monochromatic light. Peak photocontraction occurred at 450 nm. With the exception of alpha-naphthoflavone, all cytochrome P-450 inhibitors were also relaxant agents. Alpha-naphthoflavone (the sole type I inhibitor tested) produced instead a modest contraction that was often transient. Relaxation brought about by both carbon monoxide and drugs was fully reversed by the thromboxane A2 analog 9,11-epithio-11,12-methano-thromboxane A2 and by excess potassium (55 mM). Carbon monoxide was equally effective in the intact ductus and the ductus denuded of endothelium, whereas cytochrome P-450 inhibitors were marginally less effective in the latter preparation. These findings indicate that the ductus venosus sphincter, like the ductus arteriosus, relies on an intramural cytochrome P-450 mechanism to develop its contractile tone. The actual constrictor remains to be characterized in both vessels.

摘要

我们最近发现,基于细胞色素P-450的机制对于动脉导管产生收缩张力很重要,现在我们研究了同一机制是否在静脉导管中起作用。在体外对成熟胎羊的静脉导管括约肌进行了一氧化碳(CO/O₂ 比率为0.27)和细胞色素P-450抑制剂[甲吡酮;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;α-萘黄酮]测试。每个标本先用吲哚美辛(2.8×10⁻⁶ M)预收缩。一氧化碳使导管完全松弛,其作用可被单色光照射逆转。峰值光收缩出现在450 nm处。除α-萘黄酮外,所有细胞色素P-450抑制剂也是松弛剂。相反,α-萘黄酮(测试的唯一I型抑制剂)产生适度收缩,且通常是短暂的。一氧化碳和药物引起的松弛可被血栓素A₂类似物9,11-环硫-11,12-甲撑-血栓素A₂和过量钾(55 mM)完全逆转。一氧化碳在完整导管和去除内皮的导管中同样有效,而细胞色素P-450抑制剂在后者标本中的效果略差。这些发现表明,静脉导管括约肌与动脉导管一样,依赖壁内细胞色素P-450机制来产生收缩张力。两种血管中实际的收缩物质仍有待确定。

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Lamb ductus venosus: evidence of a cytochrome P-450 mechanism in its contractile tension.羔羊静脉导管:其收缩张力中细胞色素P - 450机制的证据。
J Pharmacol Exp Ther. 1990 Feb;252(2):875-9.
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