Véniant M, Clozel J P, Hess P, Wolfgang R
Pharma Division, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
J Cardiovasc Pharmacol. 1991;18 Suppl 10:S55-8.
Ro 40-5967 is a new calcium antagonist that binds to the same site as verapamil but that has been shown to have a much lesser negative inotropic effect than verapamil. The goal of the present study was to assess the hemodynamic profile of Ro 40-5967 not only in comparison with verapamil but also with diltiazem and amlodipine. For this purpose, hemodynamic parameters were assessed in conscious normotensive rats by measuring mean arterial pressure (MAP), left ventricular (LV) dP/dtmax, and heart rate. Dose-response curves were obtained with intravenous injection of the four drugs. Despite similar decreases in arterial pressure, the effects of the four drugs on left ventricular contractility and heart rate were different. Verapamil and diltiazem were markedly negative inotropic. Amlodipine decreased left ventricular contractility only at the highest dose. Ro 40-5967 was less negative inotropic than amlodipine. Verapamil, diltiazem, and Ro 40-5967 did not alter heart rate or slightly decreased it. In contrast, amlodipine induced a reflex tachycardia. In conclusion, because of its very low negative inotropism and its lack of reflex tachycardia, Ro 40-5967 seems to have a unique hemodynamic profile among calcium antagonists.
Ro 40 - 5967是一种新型钙拮抗剂,它与维拉帕米结合于同一位点,但已证明其负性肌力作用比维拉帕米小得多。本研究的目的是不仅将Ro 40 - 5967的血流动力学特征与维拉帕米进行比较,还要与地尔硫䓬和氨氯地平进行比较。为此,通过测量平均动脉压(MAP)、左心室(LV)dP/dtmax和心率,对清醒的正常血压大鼠的血流动力学参数进行评估。通过静脉注射这四种药物获得剂量 - 反应曲线。尽管动脉压下降相似,但这四种药物对左心室收缩力和心率的影响不同。维拉帕米和地尔硫䓬具有明显的负性肌力作用。氨氯地平仅在最高剂量时降低左心室收缩力。Ro 40 - 5967的负性肌力作用比氨氯地平小。维拉帕米、地尔硫䓬和Ro 40 - 5967不改变心率或使其略有下降。相比之下,氨氯地平会引起反射性心动过速。总之,由于Ro 40 - 5967极低的负性肌力作用以及缺乏反射性心动过速,它在钙拮抗剂中似乎具有独特的血流动力学特征。