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胎盘内的二磷酸腺苷降解活性。

Adenosine diphosphate-degrading activity in placenta.

作者信息

Barradas M, Khokher M, Hutton R, Craft I L, Dandona P

出版信息

Clin Sci (Lond). 1983 Feb;64(2):239-41. doi: 10.1042/cs0640239.

Abstract
  1. The degradation of ADP by the placenta and umbilical artery was investigated. 2. Supernatants from incubations of finely chopped placental and umbilical arterial tissue were incubated with [14C]ADP for various durations from 0 to 30 min. 3. Products of ADP degradation were separated by thin-layer chromatography and radioactivity incorporated into each product was measured. 4. Placental supernatants induced a more rapid degradation of ADP than the umbilical artery supernatants. The main product of ADP degradation by placental supernatants at 30 min was adenosine, whereas that of umbilical artery was AMP. 5. This conversion by placenta of ADP, a potent platelet aggregator and vasoconstrictor, into adenosine, a potent platelet anti-aggregator and vasodilator, may be important in the maintenance of perfusion of the foetoplacental unit.
摘要
  1. 研究了胎盘和脐动脉对ADP的降解情况。2. 将切碎的胎盘和脐动脉组织孵育后的上清液与[14C]ADP孵育0至30分钟不等的时间。3. 通过薄层色谱法分离ADP降解产物,并测量各产物中掺入的放射性。4. 胎盘上清液比脐动脉上清液能更快地诱导ADP降解。胎盘上清液在30分钟时使ADP降解的主要产物是腺苷,而脐动脉的主要产物是AMP。5. 胎盘将强效血小板聚集剂和血管收缩剂ADP转化为强效血小板抗聚集剂和血管扩张剂腺苷,这可能对维持胎儿-胎盘单元的灌注很重要。

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