Woodcock B G, Herrmann W, Habedank W D
Department of Clinical Pharmacology, University Clinic Frankfurt, Germany.
Int J Clin Pharmacol Ther Toxicol. 1992 Feb;30(2):63-5.
In a placebo controlled trial in 20 patients (mean age 38 years) with mild/moderate essential hypertension 4.5 mg slow-release co-dergocrine mesylate was administered once daily for 6 weeks and antihypertensive effects and plasma co-dergocrine concentrations determined 9 hours post-dose. Mean plasma co-dergocrine concentrations were 299 pg/ml, 357 pg/ml and 331 pg/ml measured after 2-, 4-, and 6-weeks administration respectively. Despite these relatively low concentrations there were statistically significant reductions in supine (-6/-6 mmHg), standing (-9/-8 mmHg) and exercise (-8/-5 mmHg) systolic and diastolic blood pressure. Blood glucose fell progressively and was 10% lower (p less than 0.02) after 6 weeks medication. Clinical and laboratory parameters showed that slow-release co-dergocrine mesylate was well tolerated with negligible adverse reactions.
在一项针对20名(平均年龄38岁)轻度/中度原发性高血压患者的安慰剂对照试验中,每天一次给予4.5毫克缓释甲磺酸麦角隐亭,持续6周,并在给药后9小时测定降压效果和血浆麦角隐亭浓度。分别在给药2周、4周和6周后测得的平均血浆麦角隐亭浓度为299 pg/ml、357 pg/ml和331 pg/ml。尽管这些浓度相对较低,但仰卧位(-6/-6 mmHg)、站立位(-9/-8 mmHg)和运动时(-8/-5 mmHg)的收缩压和舒张压均有统计学意义的降低。血糖逐渐下降,用药6周后降低了10%(p<0.02)。临床和实验室参数表明,缓释甲磺酸麦角隐亭耐受性良好,不良反应可忽略不计。