Harry J D, Linden R J, Snow H M
Br J Pharmacol. 1974 Oct;52(2):275-81. doi: 10.1111/j.1476-5381.1974.tb09710.x.
1 The effects of propranolol, oxprenolol and practolol on the isometric twitch responses to electrical stimulation of isolated diaphragm muscles from the rat and of isolated papillary muscles from the rabbit are described.2 Depression of the twitch responses of the diaphragm muscle was produced by propranolol (20 mug/ml), by oxprenolol (100 mug/ml) and by practolol (500 mug/ml).3 Depression of the twitch responses of the papillary muscles was produced by propranolol (20 mug/ml) by oxprenolol (100 mug/ml) and by practolol (200 mug/ml).4 No increase of twitch tension was produced by oxprenolol or practolol on either tissue.5 It is concluded that propranolol, oxprenolol and practolol produce negative inotropic actions on isolated cardiac muscle by a mechanism unrelated to blockade of beta-adrenoceptors and which occurs at doses which are well in excess of those doses required to produce beta-blockade.
描述了普萘洛尔、氧烯洛尔和普拉洛尔对大鼠离体膈肌及兔离体乳头肌电刺激引起的等长收缩反应的影响。
普萘洛尔(20微克/毫升)、氧烯洛尔(100微克/毫升)和普拉洛尔(500微克/毫升)可使膈肌的收缩反应减弱。
普萘洛尔(20微克/毫升)、氧烯洛尔(100微克/毫升)和普拉洛尔(200微克/毫升)可使乳头肌的收缩反应减弱。
氧烯洛尔或普拉洛尔对两种组织均未引起收缩张力增加。
得出结论:普萘洛尔、氧烯洛尔和普拉洛尔对离体心肌产生负性肌力作用,其机制与β-肾上腺素受体阻断无关,且发生在远超过产生β-阻断所需剂量的剂量水平。