KUR-1246, a novel β2-adrenoceptor agonist, as a tocolytic agent

被引:10
|
作者
Kiguchi, S
Matsuda, T
Cho, K
Okuyama, K
Akahane, M
Fujimoto, S
机构
[1] Hokkaido Univ, Sch Med, Dept Obstet & Gynecol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
[2] Hokkaido Univ, Sch Med, Dept Pediat, Sapporo, Hokkaido 0608638, Japan
[3] Kissei Pharmaceut Co Ltd, Pharmacol Res Lab, Res & Dev, Matsumoto, Nagano, Japan
来源
OBSTETRICS AND GYNECOLOGY | 2002年 / 100卷 / 03期
关键词
D O I
10.1016/S0029-7844(02)02141-5
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: To examine the effects of KUR-1246 on oxytocin-induced uterine contractions, the cardiovascular system, and general metabolism of pregnant sheep and their fetuses. METHODS: At 123-125 days' gestation, ewes (n = 8) were infused with oxytocin (1.0 mU/kg/minute) to induce uterine contractions. One hour later, KUR-1246 was infused for 3 consecutive hours beginning at a dose of 0.001 mug/kg/minute for 30 minutes and increasing stepwise every 30 minutes to 0.3 mug/kg/minute in the KUR-1246 group (n = 4). The control received saline instead (n = 4). Statistical comparisons of changes with time in the physiologic parameters between the two groups were carried out (analysis of variance). RESULTS: KUR-1246 suppressed oxytocin-induced uterine contractions more than 90% at doses over 0.03 mug/kg/minute. Significant differences between the two groups were found at high doses over 0.03 mug/kg/minute for the following parameters: maternal heart rate, diastolic blood pressure, mean blood pressure, base excess, blood K+, blood lactate, plasma glucose, plasma insulin, plasma nonesterified fatty acid levels, and fetal plasma glucose and Plasma insulin levels. CONCLUSION: KUR-1246 significantly inhibited oxytocin-induced uterine contractions at doses over 0.03 mug/kg/minute and showed reduced cardiovascular and metabolic side effects compared with ritodrine hydrochloride studied earlier in pregnant sheep. (C) 2002 by The American College of Obstetricians and Gynecologists.
引用
收藏
页码:487 / 494
页数:8
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