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某些甲基前列腺素衍生物对猪体内动脉导管的作用。

The effects of some methyl prostaglandin derivatives on the ductus arteriosus of swine in vivo.

作者信息

Starling M B, Neutze J M, Elliott R L, Taylor I M, Elliott R B

出版信息

Prostaglandins Med. 1978 Oct;1(4):267-81. doi: 10.1016/0161-4630(78)90046-0.

Abstract

Three methylated analogues of prostaglandin E1 and E2 were examined for their ability to open the ductus arterious of neonatal piglets in vivo. Fifteen (S) 15 methyl prostaglandin E1 (15-Me PGE1), 15 (S) 1K methyl prostaglandin E2 (15-Me PGE2), and 16' 16' dimethyl prostaglandin E1 (16-diMe PGE1) all opened the ductus when given intravenously, intramuscularly or orally. The effects on ductal patency lasted four hours or more in many instances. Side-effects included apnea with intravenous and intramuscular dosages, and with high oral dosages of 15-Me PGE1. A transient drop in heart rate and blood pressure occurred with each dose. In one animal the ductus was kept open for 19 days with six-hourly intramuscular injections of 3 microgram/kg 15-Me PGE1. Transient sedation occurred with each dose. Death occurred on the 19th day and histological studies showed that the morphology of the ductus wall was similar to that seen in a two day old animal. These studies suggest that maintenance od ductal patency in the infant may be possible with oral administration of methyl prostaglandin derivatives.

摘要

研究了前列腺素E1和E2的三种甲基化类似物在体内打开新生仔猪动脉导管的能力。十五(S)-15-甲基前列腺素E1(15-Me PGE1)、十五(S)-15-甲基前列腺素E2(15-Me PGE2)和16′,16′-二甲基前列腺素E1(16-二甲基PGE1)静脉内、肌内或口服给药时均能打开动脉导管。在许多情况下,对导管通畅的影响持续4小时或更长时间。副作用包括静脉内和肌内给药以及15-Me PGE1高口服剂量时出现呼吸暂停。每次给药后心率和血压都会短暂下降。在一只动物中,通过每6小时肌内注射3微克/千克的15-Me PGE1,动脉导管保持开放19天。每次给药后都会出现短暂的镇静作用。该动物在第19天死亡,组织学研究表明,动脉导管壁的形态与2日龄动物相似。这些研究表明,口服甲基前列腺素衍生物可能维持婴儿动脉导管的通畅。

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