Eigenmann R, Blaber L, Nakamura K, Thorens S, Haeusler G
Arzneimittelforschung. 1981;31(9):1393-401.
N-(3,4-Dimethoxyphenethyl)-2-(3,4-dimethoxyphenyl)-N-methyl-m-dithiane-2-propylamine-1,1,3,3-tetraoxide hydrochloride (tiapamil, Ro 11-1781), a new homoveratrylamine derivative, was studied under various experimental conditions which allow the recognition of calcium antagonistic activity, and compared with the reference calcium antagonist verapamil. Similar to verapamil, tiapamil inhibited in a concentration-dependent manner calcium-induced contractions in isolated, potassium-depolarized preparations of rat renal artery, dog coronary artery and rabbit main pulmonary artery. The inhibitory effects of tiapamil and verapamil were overcome by raising the calcium concentration of the bath fluid and a competitive antagonism between calcium ions and both compounds was found. In the rabbit main pulmonary artery both tiapamil and verapamil reduced 45Ca influx into the potassium-depolarized vascular smooth muscle cells. Calcium-mediated slowly rising potentials were evoked in partially depolarized guinea-pig papillary muscles by electrical stimulation in the presence of isoprenaline. Tiapamil, like verapamil, inhibited the slow potentials, an effect which was antagonized by elevation of the concentration of calcium or isoprenaline in the bath fluid. Both tiapamil and verapamil decreased contractile force in isolated guinea-pig atria and papillary muscles as well as in isolated cat hearts. In the last preparation the two compounds also reduced heart rate and increased coronary flow. These results characterize tiapamil as a calcium antagonist in both vascular smooth muscle and cardiac muscle. A comparison between tiapamil and verapamil indicated that both drugs are of approximately equal calcium antagonistic potency in coronary vascular smooth muscle, but verapamil is 5--10 times more potent in smooth muscle of other arterial beds and in cardiac muscle. Thus tiapamil appears to be a calcium antagonist with some preference for coronary vascular smooth muscle.
N-(3,4-二甲氧基苯乙基)-2-(3,4-二甲氧基苯基)-N-甲基间二硫杂环戊烷-2-丙胺-1,1,3,3-四氧化物盐酸盐(替帕米,Ro 11-1781)是一种新型高藜芦胺衍生物,在各种能识别钙拮抗活性的实验条件下进行了研究,并与参比钙拮抗剂维拉帕米作了比较。与维拉帕米相似,替帕米在大鼠肾动脉、犬冠状动脉和兔主肺动脉的离体钾去极化标本中,以浓度依赖方式抑制钙诱导的收缩。提高浴液钙浓度可克服替帕米和维拉帕米的抑制作用,且发现钙离子与这两种化合物之间存在竞争性拮抗。在兔主肺动脉中,替帕米和维拉帕米均可减少45Ca流入钾去极化的血管平滑肌细胞。在异丙肾上腺素存在下,通过电刺激在部分去极化的豚鼠乳头肌中诱发钙介导的缓慢上升电位。替帕米与维拉帕米一样,可抑制缓慢电位,浴液中钙或异丙肾上腺素浓度升高可拮抗这一作用。替帕米和维拉帕米均可降低离体豚鼠心房和乳头肌以及离体猫心脏的收缩力。在最后一种标本中,这两种化合物还可降低心率并增加冠脉流量。这些结果表明替帕米在血管平滑肌和心肌中均为钙拮抗剂。替帕米与维拉帕米的比较表明,两种药物在冠状血管平滑肌中的钙拮抗效力大致相当,但维拉帕米在其他动脉床平滑肌和心肌中的效力比替帕米强5至10倍。因此,替帕米似乎是一种对冠状血管平滑肌有一定偏好的钙拮抗剂。