Pittner H
Wien Klin Wochenschr Suppl. 1985;162:1-21.
The Intrinsic Sympathetic Activity (ISA) of the beta-1-adrenoceptor blocker celiprolol was tested in a series of pharmacological and clinical investigations. Celiprolol shows much more pronounced positive chronotropic effects in spontaneously beating atria of cats than in those of guinea-pigs and rats. Positive inotropic effects of celiprolol are much pronounced in the left kitten atrium, but scarcely demonstrable in the kitten papillary muscle. Celiprolol has no influence on the adenylyl cyclase activity of the dog heart. In reserpinized rats and reserpinized, adrenalectomized, vagotomized cats celiprolol increases the heart rate to the same extent as the beta-blocker pindolol. In ganglion-blocked dogs celiprolol distinctly increases heart rate and left ventricular contraction force. Celiprolol relaxes isolated human arterial and venous strips and induces a transient increase of the femoral arterial blood flow in anaesthetized dogs. Celiprolol relaxes isolated bovine tracheal muscle preparations and reduces the airway resistance in anaesthetized cats infused with serotonin. The intrinsic chronotropic effects of celiprolol in cat atria in vitro and in reserpinized rats in vivo and the relaxing effects of celiprolol in isolated bovine tracheal muscles are antagonized by propranolol, and therefore these actions may be explained by the ISA of celiprolol. However the vascular relaxing effects of celiprolol in vitro and in vivo and the bronchodilating effects in the serotonin-infused cat are not blocked by propranolol. In order to obtain a more precise characterization of these surprising effects, further pharmacological investigations were done. In the isolated femoral artery of the dog the concentration-response curve of calcium chloride is not influenced by celiprolol while it is antagonized by verapamil. A serotonin antagonistic effect cannot be demonstrated for celiprolol either in receptor binding studies or on the blood pressure of anaesthetized dogs. Celiprolol inhibits the methacholine bronchospasm in rats and the prostaglandin F2 alpha-induced bronchoconstriction in cats. The histamine-induced bronchoconstriction in dogs is scarcely affected by celiprolol while it is enhanced by propranolol. In radioligand studies celiprolol shows a tenfold higher affinity for alpha-2 in comparison to alpha-1 receptors. Celiprolol enhances the inhibitory effect of clonidine in the electrically stimulated vas deferens of the rat in vitro.(ABSTRACT TRUNCATED AT 400 WORDS)
在一系列药理和临床研究中对β1肾上腺素能阻滞剂塞利洛尔的内在交感活性(ISA)进行了测试。与豚鼠和大鼠的心房相比,塞利洛尔在猫的自主搏动心房中显示出更明显的正性变时作用。塞利洛尔的正性肌力作用在左小猫心房中更为明显,但在小猫乳头肌中几乎无法显示。塞利洛尔对犬心脏的腺苷酸环化酶活性没有影响。在利血平化大鼠以及利血平化、肾上腺切除、迷走神经切断的猫中,塞利洛尔使心率增加的程度与β受体阻滞剂吲哚洛尔相同。在神经节阻断的犬中,塞利洛尔明显增加心率和左心室收缩力。塞利洛尔使离体的人动脉和静脉条带舒张,并在麻醉犬中引起股动脉血流短暂增加。塞利洛尔使离体的牛气管肌肉制剂舒张,并降低输注血清素的麻醉猫的气道阻力。塞利洛尔在体外猫心房和体内利血平化大鼠中的内在变时作用以及在离体牛气管肌肉中的舒张作用被普萘洛尔拮抗,因此这些作用可能由塞利洛尔的ISA来解释。然而,塞利洛尔在体外和体内的血管舒张作用以及在输注血清素的猫中的支气管舒张作用未被普萘洛尔阻断。为了更精确地表征这些惊人的作用,进行了进一步的药理研究。在犬的离体股动脉中,氯化钙的浓度 - 反应曲线不受塞利洛尔影响,而维拉帕米可拮抗该曲线。在受体结合研究或麻醉犬的血压上,塞利洛尔也未显示出5 - 羟色胺拮抗作用。塞利洛尔抑制大鼠的乙酰甲胆碱支气管痉挛和猫的前列腺素F2α诱导的支气管收缩。犬的组胺诱导的支气管收缩几乎不受塞利洛尔影响,而普萘洛尔可增强该作用。在放射性配体研究中,与α1受体相比,塞利洛尔对α2的亲和力高10倍。塞利洛尔增强可乐定对体外大鼠电刺激输精管的抑制作用。(摘要截取自400字)