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[前列腺素及其他类花生酸在妊娠生理与病理生理中的意义]

[Significance of prostaglandins and other eicosanoids in the physiology and physiopathology of pregnancy].

作者信息

Lippert T H

出版信息

Geburtshilfe Frauenheilkd. 1986 Feb;46(2):71-82. doi: 10.1055/s-2008-1036166.

Abstract

Numerous investigations in animals and humans on the role of eicosanoids in pregnancy yielded the following results. During normal pregnancy, there is an increased production of eicosanoids with a vasodilatory action, prostaglandin E2 (PGE2) and prostacyclin (PGI2), especially in the uteroplacental and renal regions. This additional production contributes to a reduction in peripheral resistance so that the increase of blood volume which is specific for pregnancy can occur without increase in blood pressure. The fact that eicosanoids participate in this mechanism is shown by administration of prostaglandin synthesis inhibitors, thus producing a rise in blood pressure. In the autoregulation of the vessels, interactions between renin angiotensin and PGE2 and PGI2 are thought to play an important role also in pregnancy. In support of this concept it has been shown that the pregnancy-specific reduction in vasoconstrictor action of angiotensin, is abolished when prostaglandin synthesis inhibitors are given. It is assumed that PGE2/PGI2 production and the renin angiotensin production influence each other physiologically. Another important factor in the control of the haemodynamics and blood coagulation is represented by the prostacyclin-thromboxane system. In normal pregnancy there should be a production equilibrium between the two antagonistic eicosanoids. In preeclampsia this equilibrium, which is particularly marked in the placenta and region of the foetal vessels, is disturbed with decreasing PGI2. The main symptoms of preeclampsia--increase in blood pressure, coagulation disturbances and diminished placental circulation--can be derived from this. In diabetes and foetal growth retardation, both of which predispose to preeclampsia, similar changes in eicosanoid production have been observed. Hence, in case of preeclampsia with disturbed eicosanoid production the administration of prostaglandin synthesis inhibitors such as peripherally acting analgesics and corticoids is contraindicated. Approaches to a rational therapy such as administration of thromboxane synthesis inhibitors, a diet with prostaglandin precursors and infusions of PGI2 appear promising according to preliminary results. Further advances may be expected after the function of eicosanoids of the lipoxygenase paths in preeclampsia has been elucidated.

摘要

针对类二十烷酸在妊娠过程中所起作用,在动物和人体上开展了大量研究,得出了以下结果。在正常妊娠期间,具有血管舒张作用的类二十烷酸,即前列腺素E2(PGE2)和前列环素(PGI2)的生成量会增加,尤其是在子宫胎盘和肾脏区域。这种额外生成有助于降低外周阻力,从而使妊娠特有的血容量增加能够在不升高血压的情况下发生。给予前列腺素合成抑制剂会导致血压升高,这表明类二十烷酸参与了这一机制。在血管的自身调节中,肾素 - 血管紧张素与PGE2和PGI2之间的相互作用在妊娠过程中也被认为起着重要作用。支持这一观点的是,当给予前列腺素合成抑制剂时,妊娠特有的血管紧张素血管收缩作用减弱的现象会消失。据推测,PGE2/PGI2的生成与肾素 - 血管紧张素的生成在生理上相互影响。前列环素 - 血栓素系统是控制血流动力学和血液凝固的另一个重要因素。在正常妊娠中,这两种拮抗类二十烷酸之间应存在生成平衡。在先兆子痫中,这种平衡会受到干扰,PGI2减少,在胎盘和胎儿血管区域尤为明显。先兆子痫的主要症状——血压升高、凝血障碍和胎盘循环减少——都可由此推导得出。在糖尿病和胎儿生长受限这两种都易引发先兆子痫的情况中,也观察到了类二十烷酸生成的类似变化。因此,对于类二十烷酸生成紊乱的先兆子痫患者,禁忌使用前列腺素合成抑制剂,如外周作用的镇痛药和皮质类固醇。根据初步结果,诸如给予血栓素合成抑制剂、含有前列腺素前体的饮食以及输注PGI2等合理治疗方法似乎很有前景。在阐明先兆子痫中脂氧合酶途径的类二十烷酸功能后,有望取得进一步进展。

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