Prostacyclin production in whole blood throughout normal pregnancy.

B Spitz, H Deckmyn, F A Van Assche, J Vermylen
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引用次数: 18

Abstract

In a longitudinal study of twelve normal pregnant women the base-line plasma values of 6-keto prostaglandin (PG)F1 alpha, the stable degradation product of prostacyclin, were determined. At the same time the capacity of their blood to produce prostacyclin was assessed using a stimulation test. When collagen is added to citrated whole blood there is a prompt rise in plasma 6-keto PGF1 alpha, which results from the synthesis of prostacyclin by leukocytes. These cells use cyclic endoperoxides in part coming from activated platelets and in part derived from endogenous substrate to produce prostacyclin. Both the base-line values and the capacity to produce prostacyclin fell significantly after 33 weeks of pregnancy. The decreased capacity to produce prostacyclin in the later stages of pregnancy may help account for the relatively diminished refractoriness to angiotensin II, characterizing the last two months of normal pregnancies.

正常妊娠全血中前列环素的产生。
在一项对12名正常孕妇的纵向研究中,测定了6-酮前列腺素(PG)F1 α(前列环素的稳定降解产物)的基线血浆值。同时,他们的血液产生前列环素的能力通过刺激试验进行评估。当胶原蛋白被添加到柠檬酸全血中时,血浆6-酮PGF1 α迅速上升,这是白细胞合成前列环素的结果。这些细胞利用部分来自活化血小板的环内过氧化物和部分来自内源性底物的环内过氧化物来产生前列环素。基线值和生产前列环素的能力在怀孕33周后显著下降。妊娠后期产生前列环素的能力下降,可能有助于解释正常妊娠最后两个月血管紧张素II的耐受性相对降低的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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