Katsilambros N, Philippides P, Toskas A, Protopapas J, Frangaki D, Marangos M, Siskoudis P, Anastasopoulou K, Xefteri H, Hillebrand I
Arzneimittelforschung. 1986 Jul;36(7):1136-8.
Miglitol (Bay m 1099), a deoxynojirimycin derivative, is a new glucosidase inhibitor. The possible hypoglycemic effect of this new product was tested in 12 volunteer noninsulin-dependent diabetics (NIDDs) in a double-blind crossover acute study. The patients twice received a test meal (1554 kJ including 34 g carbohydrates), once with placebo and on another day with a 50-mg tablet of Bay m 1099. A wash-out period of 2 to 7 days separated the test days. Venous blood samples were collected before and every 30 min for a total of 3 h after the drug administration. Mean blood sugar values were in general lower after the meal + Bay m 1099 than the meal + placebo. The differences were statistically significant at the 60- and 90-min time intervals (8.43 versus 11.17 and 9.24 versus 11.59 mmol/l, respectively, p less than 0.05). No flatulence, diarrhea or other untoward effects were observed. Furthermore no changes in serum glutamic oxaloacetic transaminase, serum glutamic pyruvic transaminase, creatinine, alkaline phosphatase, bilirubin, haemoglobin, white blood count and differential counts were noted. Thus, in a one-day study 50 mg of Bay m 1099 reduced the postprandial hyperglycemia in NIDDs. No signs of any acute renal, liver and blood toxicity were observed.
米格列醇(Bay m 1099),一种脱氧野尻霉素衍生物,是一种新型糖苷酶抑制剂。在一项双盲交叉急性研究中,对12名非胰岛素依赖型糖尿病志愿者(NIDDs)测试了这种新产品可能的降血糖作用。患者两次接受试验餐(1554千焦,含34克碳水化合物),一次服用安慰剂,另一天服用50毫克Bay m 1099片剂。两次测试日之间间隔2至7天的洗脱期。给药前及给药后每30分钟采集静脉血样,共采集3小时。一般来说,餐后服用Bay m 1099后的平均血糖值低于餐后服用安慰剂后的血糖值。在60分钟和90分钟时间间隔时,差异具有统计学意义(分别为8.43对11.17以及9.24对11.59毫摩尔/升,p小于0.05)。未观察到肠胃胀气、腹泻或其他不良反应。此外,未发现血清谷草转氨酶、血清谷丙转氨酶、肌酐、碱性磷酸酶、胆红素、血红蛋白、白细胞计数及分类计数有变化。因此,在为期一天的研究中,50毫克Bay m 1099降低了NIDDs患者的餐后高血糖。未观察到任何急性肾、肝和血液毒性迹象。