首页> 美国卫生研究院文献>The Journal of Physiology >The effect of intrafetal infusion of metyrapone on arterial blood pressure and on the arterial blood pressure response to angiotensin II in the sheep fetus during late gestation
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The effect of intrafetal infusion of metyrapone on arterial blood pressure and on the arterial blood pressure response to angiotensin II in the sheep fetus during late gestation

机译:胎盘内注射甲吡酮对妊娠后期绵羊胎儿动脉血压和对血管紧张素II的动脉血压反应的影响

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摘要

While the impact of exogenous glucocorticoids on the fetal cardiovascular system has been well defined, relatively few studies have characterised the role of endogenous fetal glucocorticoids in the regulation of arterial blood pressure (BP) during late gestation. We have therefore infused metyrapone, an inhibitor of cortisol biosynthesis, into fetal sheep from 125 days gestation (when fetal cortisol concentrations are low) and from 137 days gestation (when fetal cortisol concentrations are increasing) and measured fetal plasma cortisol, 11-desoxycortisol and ACTH, fetal systolic, diastolic and mean arterial BP, heart rate, and the fetal BP responses to increasing doses of angiotensin II (AII). At 125 days gestation, there was a significant increase in fetal plasma ACTH and 11-desoxycortisol by 24 h after (+24 h) the start of the metyrapone infusion, and plasma cortisol concentrations were not different at +24 h when compared with pre-infusion values. Whilst the initial fall in circulating cortisol concentrations may have been transient, systolic, diastolic and mean arterial BP were ∼5–6 mmHg lower (P < 0.05) in metyrapone- than in vehicle-infused fetuses at 24–48 h after the start of the infusion. When metyrapone was infused from 137/138 days gestation, there was a significant decrease in plasma cortisol concentrations by +6 h, which was followed by an increase back to pre-infusion values. While cortisol concentrations decreased, there was no change in fetal mean arterial BP during the first 24 h after the start of metyrapone infusion. Mean fetal arterial BP values at 137–139 days gestation were not different in fetuses that had been infused with either vehicle or metyrapone from 125 days gestation or with metyrapone from 137–138 days gestation. At 137–139 days gestation, however, arterial BP responses to increasing doses of AII were significantly blunted in fetuses that had been infused with metyrapone from 125 days gestation, when compared with fetuses that had been infused with metyrapone from 137/138 days gestation or with vehicle from 125 days gestation. The dissociation of the gestational age increase in arterial BP and the effects of intrafetal AII on fetal arterial BP indicates that increase in fetal BP with gestational age is not entirely a result of an increased vascular responsiveness to endogenous AII. Furthermore there may be a critical window during late gestation when the actions of cortisol contribute to the development of vascular responsiveness to AII.
机译:虽然外源性糖皮质激素对胎儿心血管系统的影响已得到明确定义,但相对较少的研究已表征了内源性胎儿糖皮质激素在妊娠后期调节动脉血压(BP)中的作用。因此,我们从妊娠125天(胎儿皮质醇浓度低时)和妊娠137天(胎儿皮质醇浓度升高时)开始,向胎羊中注入了甲吡酮(皮质醇的生物合成抑制剂),并测量了胎儿血浆皮质醇,11-脱氧皮质醇和ACTH,胎儿收缩压,舒张压和平均动脉血压,心率以及胎儿BP对增加剂量的血管紧张素II(AII)的反应。妊娠125天后,甲吡酮输注开始后(+24 h)的24 h胎儿血浆ACTH和11-脱氧皮质醇显着增加,并且+24 h时的血浆皮质醇浓度没有变化。输液值。尽管开始时循环皮质醇浓度的下降可能是短暂的,但在开始治疗后24-48 h时,甲吡哌酮的收缩压,舒张压和平均动脉血压比经媒介物注入的胎儿低约5-6 mmHg(P <0.05)。输液。从妊娠137/138天开始注入甲吡酮后,血浆皮质醇浓度显着降低了+6 h,随后又回到了输注前值。尽管皮质醇浓度下降,但在甲吡酮输注开始后的最初24小时内,胎儿平均动脉血压没有变化。在妊娠125天后接受媒介物或甲吡酮或在妊娠137-138天后接受甲吡酮的胎儿在妊娠137-139天时的平均胎动脉血压值没有差异。然而,与从137/138天妊娠或137/138天输注甲吡酮的胎儿相比,在妊娠137-139天时对输注AII剂量增加的胎儿的动脉BP反应明显减弱。从妊娠125天开始使用车辆。动脉血压胎龄增加的解离和胎儿内AII对胎儿动脉血压的影响表明,胎龄增加的胎儿BP升高并非完全是由于血管对内源性AII的反应性增加所致。此外,在妊娠后期,当皮质醇的作用促进血管对AII的反应性发展时,可能会有一个重要的窗口。

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