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[The acute effects of the new angiotensin I-converting enzyme inhibitor, enalapril maleate, on blood pressure, plasma renin, aldosterone and kinins in hypertensive patients].[新型血管紧张素I转换酶抑制剂马来酸依那普利对高血压患者血压、血浆肾素、醛固酮及激肽的急性影响]
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Studies on autonomic blockade. VI. The mechanisms regulating the hemodynamic changes in the pregnant woman and their relation to the hypertension of toxemia of pregnancy.
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The effect of captopril (SQ14,225) upon mother and fetus in the chronically cannulated ewe and in the pregnant rabbit.卡托普利(SQ14,225)对长期插管母羊和怀孕兔子的母体及胎儿的影响。
J Physiol. 1982 Feb;323:415-22. doi: 10.1113/jphysiol.1982.sp014081.
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Transfer of propranolol and sotalol across the human placenta. Their effect on maternal and fetal plasma renin activity.普萘洛尔和索他洛尔通过人胎盘的转运及其对母体和胎儿血浆肾素活性的影响。
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Captopril-induced changes in prostaglandin production: relationship to vascular responses in normal man.卡托普利引起的前列腺素生成变化:与正常男性血管反应的关系。
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Atenolol: side effects in a newborn infant.阿替洛尔:一名新生儿的副作用。
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Effect of captopril on uterine blood flow and prostaglandin E synthesis in the pregnant rabbit.卡托普利对孕兔子宫血流量及前列腺素E合成的影响。
J Clin Invest. 1983 Apr;71(4):809-15. doi: 10.1172/jci110834.
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Enalapril (MK421) and its lysine analogue (MK521): a comparison of acute and chronic effects on blood pressure, renin-angiotensin system and sodium excretion in normal man.依那普利(MK421)及其赖氨酸类似物(MK521):对正常男性血压、肾素-血管紧张素系统及钠排泄的急性和慢性影响比较
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Enalapril maleate (MK-421), a potent, nonsulfhydryl angiotensin-converting enzyme inhibitor: absorption, disposition, and metabolism in man.马来酸依那普利(MK-421),一种强效非巯基血管紧张素转换酶抑制剂:人体中的吸收、分布及代谢
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血管紧张素转换酶抑制剂依那普利(MK421)对清醒妊娠母羊及其胎儿的影响。

The effect of enalapril (MK421), an angiotensin converting enzyme inhibitor, on the conscious pregnant ewe and her foetus.

作者信息

Broughton Pipkin F, Wallace C P

出版信息

Br J Pharmacol. 1986 Mar;87(3):533-42. doi: 10.1111/j.1476-5381.1986.tb10195.x.

DOI:10.1111/j.1476-5381.1986.tb10195.x
PMID:3026539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1916568/
Abstract

The effects of enalapril, an angiotensin converting enzyme (ACE) inhibitor, on maternal and foetal blood pressure, heart rate and components of the renin-angiotensin-aldosterone system were studied in 9 chronically-cannulated pregnant ewes and their foetuses. Six ewes received 1 mg kg-1 enalapril i.v. while 3 were given 2 mg kg-1. Although the initial fall in blood pressure was slightly greater in the higher dose group, there was substantial overlap of data. The pressor response to angiotensin I, assessing ACE activity, was abolished within 10 min of administration, and did not recover during 3 h of observation. Maternal systolic and diastolic pressures reached a nadir 90 min after administration (P less than 0.001, P less than 0.002 respectively). The maximum tachycardia was seen at 60 min (P less than 0.05). The foetuses of the ewes given 1 mg kg-1 enalapril showed no change in systolic or diastolic blood pressure or heart rate. Those of the ewes given the higher dose showed late-onset hypotension, coincident with the lowest maternal blood pressures. Maternal plasma renin concentration (PRC) had risen significantly by 30 min (P less than 0.02), reaching a maximum at approximately 90 min. Maternal plasma angiotensin II and aldosterone concentrations both fell initially (P less than 0.05) but were almost at basal levels by the end of the experiment. Foetal plasma renin, angiotensin II and aldosterone concentrations were unchanged throughout the experiment. Peak values of enaprilic acid, the active principle, were recorded in maternal plasma 65-90 min after administration of 1 mg kg-1, and 25-30 min after the administration of 2 mg kg-1. A trace amount of the active principle was recorded in the foetal plasma of one lamb, whose mother had been given the higher dose. None was recorded in the plasma from three other lambs. Maternal plasma ACE concentrations fell by an average of 84%; in 4 of the 6 ewes in which concentrations were measured they were undetectable after treatment. Foetal plasma ACE concentrations were unchanged throughout. Enalapril at 1 mg kg-1 thus exerts a depressor effect on the pregnant ewe which is probably related to its blockade of the renin-angiotensin system. Both direct measurement of the drug and foetal observation suggest that it does not cross the sheep placenta at this dose. This is consistent with its failure to cross the blood-brain barrier. Foetal effects were noted at 2 mg kg-1, and there was an unexpected foetal death in this group.

摘要

在9只长期插管的怀孕母羊及其胎儿身上,研究了血管紧张素转换酶(ACE)抑制剂依那普利对母羊和胎儿血压、心率以及肾素 - 血管紧张素 - 醛固酮系统各组分的影响。6只母羊静脉注射1mg/kg依那普利,3只母羊静脉注射2mg/kg。虽然高剂量组血压的初始下降幅度略大,但数据有大量重叠。给药后10分钟内,评估ACE活性的血管紧张素I升压反应消失,在3小时观察期内未恢复。给药后90分钟,母羊收缩压和舒张压降至最低点(分别为P<0.001,P<0.002)。最大心动过速出现在60分钟(P<0.05)。静脉注射1mg/kg依那普利的母羊所产胎儿的收缩压、舒张压或心率均无变化。给予高剂量依那普利的母羊所产胎儿出现迟发性低血压,与母羊最低血压同时出现。母羊血浆肾素浓度(PRC)在30分钟时显著升高(P<0.02),约90分钟时达到最高值。母羊血浆血管紧张素II和醛固酮浓度最初均下降(P<0.05),但实验结束时几乎恢复到基础水平。整个实验过程中,胎儿血浆肾素、血管紧张素II和醛固酮浓度均无变化。静脉注射1mg/kg依那普利后,活性成分依那普利酸在母羊血浆中的峰值出现在给药后65 - 90分钟;静脉注射2mg/kg依那普利后,峰值出现在给药后25 - 30分钟。在一只母羊给予高剂量依那普利后所产羔羊的胎儿血浆中记录到微量活性成分,另外三只羔羊的血浆中未记录到。母羊血浆ACE浓度平均下降84%;在6只测量浓度的母羊中,有4只在治疗后无法检测到。整个实验过程中,胎儿血浆ACE浓度无变化。因此,1mg/kg依那普利对怀孕母羊有降压作用,这可能与其阻断肾素 - 血管紧张素系统有关。药物的直接测量和胎儿观察均表明,此剂量下依那普利不会穿过绵羊胎盘。这与其不能穿过血脑屏障一致。在2mg/kg剂量下观察到了对胎儿的影响,该组出现了1例意外的胎儿死亡。