Hahn D W, McGuire J L, Vanderhoof M, Ericson E, Pasquale S A
Am J Obstet Gynecol. 1984 Mar 15;148(6):775-8. doi: 10.1016/0002-9378(84)90565-9.
Reported are pharmacologic data from a new animal model used for evaluating drugs from several therapeutic classes for their potential use in the treatment of premature labor. This model measures the spontaneous delivery time between the first and second rat pups in a term pregnancy. In control animals, this averaged 16.3 +/- 4.2 minutes. Ethanol (3.5 gm/kg) and the beta-agonists ritodrine (12.5 mg/kg) and albuterol (0.25 mg/kg) significantly delayed delivery of the second pup. The calcium blockers nifedipine, verapamil, and diltiazem were the most active of all compounds tested in this model. The nonsteroidal anti-inflammatory agents indomethacin and naproxen were inactive at doses as high as 5 and 25 mg/kg, respectively. Metiamide, an H2-antagonist, and dimenhydrinate, an H1-antagonist, were inactive.
报道了一种新的动物模型的药理学数据,该模型用于评估来自几个治疗类别的药物在治疗早产方面的潜在用途。该模型测量足月妊娠大鼠第一只和第二只幼崽之间的自然分娩时间。在对照动物中,这一平均时间为16.3±4.2分钟。乙醇(3.5克/千克)、β-激动剂利托君(12.5毫克/千克)和沙丁胺醇(0.25毫克/千克)显著延迟了第二只幼崽的分娩。钙通道阻滞剂硝苯地平、维拉帕米和地尔硫䓬是该模型中测试的所有化合物中活性最高的。非甾体抗炎药吲哚美辛和萘普生分别在高达5毫克/千克和25毫克/千克的剂量下无活性。H2拮抗剂甲硫米特和H1拮抗剂茶苯海明无活性。