Lewis H M, Kendall M J, Wright A D, Bratty J R, Maxwell S
Department of Medicine, Medical School, Edgbaston, Birmingham, U.K.
J Clin Pharm Ther. 1991 Jun;16(3):161-6. doi: 10.1111/j.1365-2710.1991.tb00299.x.
The effects of steady-state flosequinan, a new peripheral vasodilator, and propranolol on glucose tolerance and plasma lipids in 22 non-insulin-dependent diabetics were investigated in a randomized double-blind placebo-controlled, three-way crossover trial. Flosequinan produced no impairment of glucose tolerance compared with placebo. Propranolol produced significant increases in fasting plasma glucose (P less than 0.01) and increases in the area under the glucose tolerance curve (P less than 0.05) compared to placebo. No significant effects on cholesterol levels were seen on either treatment but triglyceride levels were significantly elevated on propranolol compared with placebo (P less than 0.01). These data suggest that flosequinan, used in therapeutic dosage, has no adverse metabolic effects on the non-insulin-dependent diabetic and this may be an advantage for a drug used in the treatment of hypertension or congestive heart failure.
在一项随机双盲安慰剂对照的三向交叉试验中,研究了新型外周血管扩张剂稳态氟司喹南和普萘洛尔对22名非胰岛素依赖型糖尿病患者糖耐量和血脂的影响。与安慰剂相比,氟司喹南未损害糖耐量。与安慰剂相比,普萘洛尔使空腹血糖显著升高(P<0.01),糖耐量曲线下面积增加(P<0.05)。两种治疗对胆固醇水平均无显著影响,但与安慰剂相比,普萘洛尔使甘油三酯水平显著升高(P<0.01)。这些数据表明,治疗剂量的氟司喹南对非胰岛素依赖型糖尿病患者无不良代谢影响,这对于用于治疗高血压或充血性心力衰竭的药物可能是一个优势。