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Randomised comparison of methyldopa and oxprenolol for treatment of hypertension in pregnancy.甲基多巴与氧烯洛尔治疗妊娠期高血压的随机对照研究。
Br Med J. 1979 Jun 16;1(6178):1591-4. doi: 10.1136/bmj.1.6178.1591.

本文引用的文献

1
EPINEPHRINE DERIVATES AND THE ACTIVITY OF THE HUMAN UTERUS. II. THE INFLUENCE OF PRONETHALOL AND PROPANOLOLT ON THE UTERINE AND SYSTEMIC ACTIVITY OF P-HYDROXYPHENYLISOPROPYLARTERENOL (CC-25).肾上腺素衍生物与人体子宫的活性。II. 心得安和普萘洛尔对间羟异丙肾上腺素(CC-25)子宫及全身活性的影响
Am J Obstet Gynecol. 1965 Jul 15;92:871-81. doi: 10.1016/s0002-9378(16)34796-2.
2
EPINEPHRINE DERIVATES AND THE ACTIVITY OF THE HUMAN UTERUS. I. . THE INHIBITING EFFECT OF P-HYDROXYPHENYLISOPROPYLARTERENOL (CC-25) UPON UTERINE ACTIVITY IN HUMAN PREGNANCY.
Am J Obstet Gynecol. 1965 Jul 15;92:865-70. doi: 10.1016/s0002-9378(16)34795-0.
3
Effects of adrenergic blocking agents and catecholamines in human pregnancy.肾上腺素能阻滞剂和儿茶酚胺在人类妊娠中的作用。
Am J Obstet Gynecol. 1968 Sep 15;102(2):226-35. doi: 10.1016/0002-9378(68)90323-2.
4
Chronic exteriorization of vascular cannulas and ECG electrodes from the ovine fetus.绵羊胎儿血管插管和心电图电极的慢性外置化。
J Appl Physiol. 1970 Feb;28(2):248-50. doi: 10.1152/jappl.1970.28.2.248.
5
Effect of adrenergic receptor-blocking drugs in pregnancy in rats.肾上腺素能受体阻断药物对大鼠孕期的影响。
J Reprod Fertil. 1970 Apr;21(3):551-4. doi: 10.1530/jrf.0.0210551.
6
Beta-adrenoceptive responses in the unanaesthetized ovine foetus.未麻醉绵羊胎儿的β-肾上腺素能反应。
Br J Pharmacol. 1970 May;38(3):572-82. doi: 10.1111/j.1476-5381.1970.tb10598.x.
7
The effect of blockade of the beta receptors of the sympathetic nervous system of the fetus. A preliminary report.胎儿交感神经系统β受体阻断的效应。初步报告。
Acta Obstet Gynecol Scand. 1969;48(S3):75-9. doi: 10.3109/00016346909157714.
8
The effect of propranolol on the onset of breathing at birth.普萘洛尔对出生时呼吸开始的影响。
Br J Anaesth. 1969 Sep;41(9):792.
9
Inhibition of drug-metabolizing enzymes of liver microsomes by hydrazine derivatives in relation to their lipid solubility.肼衍生物对肝微粒体药物代谢酶的抑制作用与其脂溶性的关系。
Jpn J Pharmacol. 1969 Jun;19(2):315-22. doi: 10.1254/jjp.19.315.
10
Perspectives in adrenergic beta-receptor blockade.肾上腺素能β受体阻滞剂的展望
Clin Pharmacol Ther. 1969 May-Jun;10(3):292-306. doi: 10.1002/cpt1969103292.

几种β-肾上腺素能受体阻断药物对妊娠绵羊和胎儿的作用。

Action of several -adrenoceptor blocking drugs in the pregnant sheep and foetus.

作者信息

Truelove J F, van Petten G R, Willes R F

出版信息

Br J Pharmacol. 1973 Jan;47(1):161-71. doi: 10.1111/j.1476-5381.1973.tb08170.x.

DOI:10.1111/j.1476-5381.1973.tb08170.x
PMID:4146153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1776527/
Abstract
  1. The effect of several beta-adrenoceptor blocking drugs on the pregnant ewe and foetus were studied. Bunolol, butidrine, oxprenolol, propranolol and USVP65-24 all crossed the ovine placenta and produced a beta-adrenoceptor blockade in the ovine foetus. AH3474, AY21011 and sotalol did not cross the ovine placenta as assessed by the absence of a beta-blockade in the foetus when these compounds were administered to the pregnant ewe.2. Of the beta-blocking compounds tested, only propranolol and oxprenolol produced a prolonged blockade in the foetus. The beta-blockade with propranolol was of 3 h duration in the ewe and 10 h duration in the foetus. Oxprenolol produced a beta-blockade of 3 h duration in the ewe and 8 h in the foetus.3. The beta-blocking drugs which did cross the ovine placenta were more soluble in organic solvents (ether, chloroform, corn oil and olive oil) than those which did not cross the ovine placenta.
摘要
  1. 研究了几种β-肾上腺素能受体阻断药物对妊娠母羊和胎儿的影响。布诺洛尔、布替林、氧烯洛尔、普萘洛尔和USVP65 - 24均能穿过绵羊胎盘,并在绵羊胎儿体内产生β-肾上腺素能受体阻断作用。当给妊娠母羊施用AH3474、AY21011和索他洛尔时,由于胎儿体内未出现β-阻断作用,表明它们未穿过绵羊胎盘。

  2. 在测试的β-阻断化合物中,只有普萘洛尔和氧烯洛尔在胎儿体内产生了持久的阻断作用。普萘洛尔对母羊的β-阻断作用持续3小时,对胎儿持续10小时。氧烯洛尔对母羊的β-阻断作用持续3小时,对胎儿持续8小时。

  3. 能穿过绵羊胎盘的β-阻断药物比不能穿过绵羊胎盘的药物在有机溶剂(乙醚、氯仿、玉米油和橄榄油)中的溶解度更高。