Velasco M, Hurt E, Silva H, Urbina-Quintana A, Hernández-Pieretti O, Feldstein E, Camejo G
Am J Med. 1986 Feb 14;80(2A):109-13. doi: 10.1016/0002-9343(86)90169-5.
Prazosin and propranolol were compared in an open, crossover study to determine their effects on plasma lipids and lipoproteins. After a four-week placebo period, 10 hypertensive patients were randomly assigned to prazosin treatment (Group I) and another 10 to propranolol treatment (Group II) for eight weeks. After a second four-week placebo period, treatment in each group was switched to the alternative drug for eight weeks. The mean blood pressure was reduced to normal levels (diastolic blood pressure less than or equal to 90 mm Hg) by both drugs--prazosin (1 to 8 mg per day) and propranolol (40 to 240 mg per day). The results of the study indicate that prazosin decreases serum cholesterol levels. In contrast, propranolol not only increases serum triglyceride levels and very-low-density lipoprotein cholesterol, but decreases total high-density lipoprotein cholesterol, high-density lipoprotein2 cholesterol, high-density lipoprotein2, and apoprotein A-I. The data suggest that propranolol may induce significant, potentially atherogenic changes in lipid metabolism, whereas prazosin may represent an advantageous alternative as an antihypertensive agent, especially in subjects with an already atherogenic lipoprotein profile.
在一项开放性交叉研究中,对哌唑嗪和普萘洛尔进行了比较,以确定它们对血浆脂质和脂蛋白的影响。经过为期四周的安慰剂期后,10名高血压患者被随机分配接受哌唑嗪治疗(第一组),另外10名接受普萘洛尔治疗(第二组),为期八周。经过第二个为期四周的安慰剂期后,每组的治疗更换为另一种药物,持续八周。两种药物——哌唑嗪(每日1至8毫克)和普萘洛尔(每日40至240毫克)均将平均血压降至正常水平(舒张压小于或等于90毫米汞柱)。研究结果表明,哌唑嗪可降低血清胆固醇水平。相比之下,普萘洛尔不仅会升高血清甘油三酯水平和极低密度脂蛋白胆固醇,还会降低总高密度脂蛋白胆固醇、高密度脂蛋白2胆固醇、高密度脂蛋白2和载脂蛋白A-I。数据表明,普萘洛尔可能会在脂质代谢中引发显著的、潜在的致动脉粥样硬化变化,而哌唑嗪作为一种抗高血压药物可能是一种更具优势的选择,尤其是对于那些已经具有致动脉粥样硬化脂蛋白谱的患者。