Kageyama M, Nishimura K, Takada T, Miyawaki N, Yamauchi H
Central Research Laboratories, Santen Pharmaceutical Co., Ltd., Osaka, Japan.
J Cardiovasc Pharmacol. 1991 Jan;17(1):102-7. doi: 10.1097/00005344-199101000-00015.
We compared the effects of SD-3211, a novel calcium antagonist, on blood pressure, heart rate, and atrioventricular conduction with those of diltiazem using conscious renal hypertensive dogs (one-kidney, one-clip type). We also examined the combined effects of these calcium antagonists with a beta-adrenoceptor antagonist, propranolol, on these variables. Oral administration of SD-3211 (1.25, 2.5, and 5 mg/kg) resulted in a dose-dependent decrease in blood pressure without affecting heart rate. SD-3211 at all three doses significantly decreased systolic blood pressure. At 2.5 and 5 mg/kg the compound elicited significant decreases in mean blood pressure and diastolic blood pressure. Hypotension obtained with the highest dose of SD-3211 lasted for at least 9 h. No significant alteration in PR interval was observed in electrocardiograms after administration of SD-3211. Diltiazem, given orally at doses of 2.5 and 5 mg/kg but not 1.25 mg/kg, produced significant hypotension with little change in heart rate. The duration of hypotension induced by the highest dose of diltiazem was only 3 h. Diltiazem prolonged PR interval in a dose-dependent manner, causing second-degree atrioventricular block in some dogs. Combined administration of SD-3211 or diltiazem (2.5 mg/kg) with propranolol (30 mg/kg) resulted in enhanced hypotension with no alteration in heart rate. SD-3211 plus propranolol had little effect on the PR interval, whereas diltiazem plus propranolol caused a markedly enhanced prolongation. These results indicate that SD-3211 is an antihypertensive agent with long-lasting action and little effect on heart rate and atrioventricular conduction and, when administered alone or in combination with propranolol, may be useful in the treatment of hypertension.
我们使用清醒的肾性高血压犬(单肾、单夹型),比较了新型钙拮抗剂SD - 3211与地尔硫䓬对血压、心率及房室传导的影响。我们还研究了这些钙拮抗剂与β - 肾上腺素能受体拮抗剂普萘洛尔联合应用对上述指标的影响。口服SD - 3211(1.25、2.5和5mg/kg)导致血压呈剂量依赖性下降,而心率不受影响。SD - 3211的所有三个剂量均显著降低收缩压。在2.5和5mg/kg时,该化合物可显著降低平均血压和舒张压。SD - 3211最高剂量引起的低血压持续至少9小时。给予SD - 3211后,心电图的PR间期未观察到明显改变。口服2.5和5mg/kg但非1.25mg/kg剂量的地尔硫䓬可产生显著低血压,心率变化不大。地尔硫䓬最高剂量引起的低血压持续时间仅为3小时。地尔硫䓬以剂量依赖性方式延长PR间期,在一些犬中导致二度房室传导阻滞。SD - 3211或地尔硫䓬(2.5mg/kg)与普萘洛尔(30mg/kg)联合给药导致低血压增强,心率无改变。SD - 3211加普萘洛尔对PR间期影响不大,而地尔硫䓬加普萘洛尔则导致PR间期显著延长。这些结果表明,SD - 3211是一种具有长效作用且对心率和房室传导影响较小的抗高血压药物,单独或与普萘洛尔联合使用时,可能对高血压治疗有用。