Harter H R, Meltzer V N, Tindira C A, Naumovich A D, Goldberg A P
Am J Med. 1986 Feb 14;80(2A):82-9. doi: 10.1016/0002-9343(86)90164-6.
A prospective, crossover study was used to evaluate the effects of prazosin and propranolol on lipid metabolism in 10 hypertensive patients receiving long-term hemodialysis therapy. Adequate blood pressure control was achieved with either agent (mean predialysis blood pressure was 144/77 mm Hg). Total triglyceride levels increased by 27 +/- 4 percent during propranolol therapy but decreased during prazosin therapy by 8 +/- 2 percent (p less than 0.05). These changes were accounted for by a 21 +/- 1.5 percent increase in very-low-density lipoprotein triglyceride during propranolol therapy and a 6 +/- 2 percent decrease in very-low-density lipoprotein triglyceride during prazosin therapy (p less than 0.05). Although no change in total cholesterol occurred with either agent, a significant decrease (19 +/- 1 percent, p less than 0.01) in high-density lipoprotein cholesterol occurred with propranolol therapy and an increase of 16 +/- 4 percent occurred during treatment with prazosin (not significant). The high-density lipoprotein2 cholesterol levels decreased by 22 +/- 4 percent after treatment with propranolol and increased by 4 percent after prazosin therapy. Propranolol reduced high-density lipoprotein3 cholesterol levels by 18 +/- 2 percent, whereas prazosin increased these values by 19 +/- 2 percent (p less than 0.01). These changes were associated with a reduction in tissue lipoprotein lipase activity after propranolol therapy (2.4 +/- 0.3 percent) and an increase after prazosin therapy (2.5 +/- 1 percent, p less than 0.05). These data suggest that treatment with propranolol may be associated with unfavorable changes in the lipid profile that are not observed after treatment with prazosin.
一项前瞻性交叉研究用于评估哌唑嗪和普萘洛尔对10例接受长期血液透析治疗的高血压患者脂质代谢的影响。两种药物均实现了充分的血压控制(透析前平均血压为144/77 mmHg)。在普萘洛尔治疗期间,总甘油三酯水平升高了27±4%,而在哌唑嗪治疗期间降低了8±2%(p<0.05)。这些变化是由于普萘洛尔治疗期间极低密度脂蛋白甘油三酯增加了21±1.5%,而哌唑嗪治疗期间极低密度脂蛋白甘油三酯降低了6±2%(p<0.05)。虽然两种药物治疗后总胆固醇均无变化,但普萘洛尔治疗后高密度脂蛋白胆固醇显著降低(19±1%,p<0.01),而哌唑嗪治疗期间升高了16±4%(无统计学意义)。普萘洛尔治疗后高密度脂蛋白2胆固醇水平降低了22±4%,哌唑嗪治疗后升高了4%。普萘洛尔使高密度脂蛋白3胆固醇水平降低了18±2%,而哌唑嗪使这些值升高了19±2%(p<0.01)。这些变化与普萘洛尔治疗后组织脂蛋白脂肪酶活性降低(2.4±0.3%)以及哌唑嗪治疗后升高(2.5±1%,p<0.05)有关。这些数据表明,普萘洛尔治疗可能与脂质谱的不良变化有关,而哌唑嗪治疗后未观察到这种情况。