Strano A, Novo S, Raineri A, Alaimo G, Abrignani M G, Cutietta A
J Hypertens Suppl. 1986 Apr;4(1):S103-6.
Ketanserin is a new potent antiserotonergic drug which, unlike previous ones, is selective for S2-serotoninergic receptors and does not have an agonist action. A trial was carried out on medium-term treatment with ketanserin or propranolol in subjects suffering from mild to moderate hypertension. The trial was designed as a double-blind crossover randomized study comparing either ketanserin or propranolol with placebo. Thirteen patients completed the study, which was divided into two groups (A and B). Systolic (SBP), diastolic (DBP) and mean (MBP) blood pressures were measured by non-invasive, intermittent ambulatory monitoring performed using a Pressurometer II, from Del Mar Avionics. Heart rate was measured using a continuous electrocardiogram monitoring. Systolic blood pressure was significantly reduced both after ketanserin (A:11.1%; B:10.8%) and propranolol (A:11.7%; B:11.8%) but in group A its decrease was more pronounced after propranolol (P less than 0.01). Diastolic blood pressure was significantly reduced both after ketanserin (A:11.5%; B:11.1%) and propranolol (A:11.4%; B:11.9%), as was MBP (A:11.9%; B:11.8% for ketanserin and A:11.9%; B:11.9% for propranolol). The heart rate diminished significantly only after propranolol administration (P less than 0.01). Ambulatory monitoring showed a significant 24-h reduction of SBP after administration of propranolol (P less than 0.0025) and ketanserin (A:P less than 0.0025, B: P less than 0.005). Diastolic blood pressure was also significantly reduced after ketanserin (P less than 0.0005) and propranolol (A: P less than 0.0025, B: P less than 0.0005). The heart rate obtained by continuous electrocardiogram monitoring diminished significantly only after propranolol administration (P less than 0.0005). No significant changes of circadian behaviour of blood pressure were observed.
酮色林是一种新型强效抗血清素能药物,与以往药物不同,它对S2 - 血清素能受体具有选择性,且无激动剂作用。对患有轻至中度高血压的受试者进行了酮色林或普萘洛尔中期治疗试验。该试验设计为双盲交叉随机研究,将酮色林或普萘洛尔与安慰剂进行比较。13名患者完成了研究,研究分为两组(A组和B组)。收缩压(SBP)、舒张压(DBP)和平均血压(MBP)通过使用德尔马航空电子公司的Pressurometer II进行的非侵入性间歇动态监测来测量。心率通过连续心电图监测来测量。服用酮色林后(A组:11.1%;B组:10.8%)和普萘洛尔后(A组:11.7%;B组:11.8%)收缩压均显著降低,但在A组中,服用普萘洛尔后收缩压下降更为明显(P小于0.01)。服用酮色林后(A组:11.5%;B组:11.1%)和普萘洛尔后(A组:11.4%;B组:11.9%)舒张压均显著降低,平均血压也是如此(酮色林A组:11.9%;B组:11.8%,普萘洛尔A组:11.9%;B组:11.9%)。仅在服用普萘洛尔后心率显著降低(P小于0.01)。动态监测显示,服用普萘洛尔后24小时收缩压显著降低(P小于0.0025),服用酮色林后也显著降低(A组:P小于0.0025,B组:P小于0.005)。服用酮色林(P小于0.0005)和普萘洛尔后(A组:P小于0.0025,B组:P小于0.0005)舒张压也显著降低。通过连续心电图监测获得的心率仅在服用普萘洛尔后显著降低(P小于0.0005)。未观察到血压昼夜行为的显著变化。