Bayer B L, Förster W, Sperling J
Arch Int Pharmacodyn Ther. 1976 Jun;221(2):328-8.
The effects of PGE1, PGE2 and PGF2alpha on conduction time and functional refractory period in the isolated rabbit atrium and in the cat heart in vivo were investigated. In the isolated rabbit atrium the PGs (10(-8)--10(-5) g/ml) were without any effect in this respect. In contrast there was a dose-dependent decrease of conduction time and prolongation of functional refractory period in the cat heart in vivo following PG-infusions (2,0--8,0 mug/kg/min i.v. over a period of 5 min). These findings indicate the absence of a direct quinidine-like membrane action of PGs in the heart. The indirect, depressive effects of PGs on conduction time and functional refractory period in the heart in vivo, should be considered responsible for the antiarrhythmic action of PGs.
研究了前列腺素E1、前列腺素E2和前列腺素F2α对离体兔心房及猫活体心脏传导时间和功能不应期的影响。在离体兔心房中,前列腺素(10⁻⁸ - 10⁻⁵ g/ml)在这方面没有任何作用。相反,在猫活体心脏中静脉输注前列腺素(2.0 - 8.0 μg/kg/min,持续5分钟)后,传导时间呈剂量依赖性缩短,功能不应期延长。这些发现表明前列腺素在心脏中不存在类似奎尼丁的直接膜作用。前列腺素对活体心脏传导时间和功能不应期的间接抑制作用,应被认为是其抗心律失常作用的原因。