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曲莫前列素(三甲基脱氧前列腺素E2)对女性子宫内压的影响。

The effect of trimoprostil (trimethyldesoxy prostaglandin E2) on the intrauterine pressure in women.

作者信息

Reele S B, Nauss-Karol C, Lusaitis A A, Passe S M

机构信息

Department of Clinical Research and Development, Hoffmann-La Roche Inc., Nutley, NJ 07110.

出版信息

Clin Pharmacol Ther. 1988 Aug;44(2):179-85. doi: 10.1038/clpt.1988.134.

DOI:10.1038/clpt.1988.134
PMID:3293873
Abstract

Prostaglandin E2 is uterotonic. Trimoprostil, a prostaglandin E2 analog, is a gastric antisecretory and cytoprotective agent. The effects of single doses of 0, 0.125, 0.75, and 3.0 mg trimoprostil on intrauterine pressure were measured in a double-blind, crossover study in eight surgically sterile women. The 3 mg dose was not tolerated because of abdominal cramps. The other doses caused a dose-related increase in resting uterine tone and peak pressure with peak effect occurring between 30 and 60 minutes after administration with a duration of about 120 minutes. No effects on the frequency of uterine contractions occurred. Peak mean tone increased from 11.0 to 71.2 mm Hg (p less than 0.01) and peak pressure from 24.6 to 125.1 mm Hg (p less than 0.01) after placebo compared with the 1.5 mg dose. Adverse reactions included abdominal pain that correlated with an increase in intrauterine pressure and tone.

摘要

前列腺素E2具有子宫收缩作用。曲莫前列素是一种前列腺素E2类似物,是一种胃抗分泌和细胞保护剂。在一项针对8名手术绝育女性的双盲交叉研究中,测量了单剂量0、0.125、0.75和3.0毫克曲莫前列素对子宫内压的影响。3毫克剂量因腹部绞痛而无法耐受。其他剂量导致静息子宫张力和峰值压力呈剂量相关增加,给药后30至60分钟出现峰值效应,持续时间约120分钟。对子宫收缩频率无影响。与1.5毫克剂量相比,安慰剂后平均峰值张力从11.0毫米汞柱增加到71.2毫米汞柱(p小于0.01),峰值压力从24.6毫米汞柱增加到125.1毫米汞柱(p小于0.01)。不良反应包括与子宫内压和张力增加相关的腹痛。

相似文献

1
The effect of trimoprostil (trimethyldesoxy prostaglandin E2) on the intrauterine pressure in women.曲莫前列素(三甲基脱氧前列腺素E2)对女性子宫内压的影响。
Clin Pharmacol Ther. 1988 Aug;44(2):179-85. doi: 10.1038/clpt.1988.134.
2
Effects of acute administration of a prostaglandin E2 analog, trimoprostil, on esophageal motility in man.前列腺素E2类似物曲莫前列素急性给药对人体食管动力的影响。
Am J Gastroenterol. 1987 Sep;82(9):836-9.
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[Intragastric acidity under the prostaglandin E2 analog trimoprostil. Increased inhibitory effect through administration after meals].[前列腺素E2类似物曲莫前列素作用下的胃内酸度。餐后给药增强抑制作用]
Arzneimittelforschung. 1986 Mar;36(3):500-2.
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Acute and chronic effects of oral enprostil, a synthetic dehydroprostaglandin E2, on uterine contractility.口服恩前列素(一种合成的脱氢前列腺素E2)对子宫收缩性的急性和慢性影响。
Prostaglandins Leukot Essent Fatty Acids. 1989 Apr;36(1):15-9. doi: 10.1016/0952-3278(89)90156-7.
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Trimoprostil plasma concentration-gastric acid inhibition relationships in duodenal ulcer patients.十二指肠溃疡患者中曲莫前列素血浆浓度与胃酸抑制的关系。
J Clin Pharmacol. 1986 Jan;26(1):48-54. doi: 10.1002/j.1552-4604.1986.tb02902.x.
6
Lack of effect of arbaprostil on the human non-pregnant uterus.阿巴前列素对人非妊娠子宫无作用。
Acta Obstet Gynecol Scand. 1985;64(8):645-7. doi: 10.3109/00016348509158206.
7
A multicentre comparison of trimoprostil and cimetidine in the treatment of duodenal ulcer. U.K. Trimoprostil Study Collaborative Group.曲莫前列素与西咪替丁治疗十二指肠溃疡的多中心比较。英国曲莫前列素研究协作组。
Scand J Gastroenterol. 1988 Mar;23(2):134-8. doi: 10.3109/00365528809103957.
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[Anti-ulcerogenic and cytoprotective effects of trimoprostil (Ro 21-6937), a trimethylprostaglandin E2 derivative].三甲基前列腺素E2衍生物曲莫前列素(Ro 21-6937)的抗溃疡和细胞保护作用
Nihon Yakurigaku Zasshi. 1983 Aug;82(2):131-47.
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Trimoprostil plasma concentration--gastric acid inhibition relationships: potentiation by food.曲莫前列素血浆浓度与胃酸抑制的关系:食物的增强作用
Clin Pharmacol Ther. 1985 Feb;37(2):113-7. doi: 10.1038/clpt.1985.21.
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Trimoprostil decreases acid disappearance from the human stomach.曲莫前列素可减少胃酸从人胃中的消失。
Curr Med Res Opin. 1986;10(5):308-12. doi: 10.1185/03007998609111095.