Matzkies F, Stechert R, Rauber G, Matzkies F, Drescher U
Kurparkklinik, Bad Neustadt/Saale und Boehringer Ingelheim KG, Abteilung Medizin, Ingelheim, Rhein.
Arzneimittelforschung. 1989 Sep;39(9):1171-2.
For eight days 8 healthy volunteers were treated with a formula diet and additional 1680 purine base per day. Beginning with day 5, doqualast was administered orally in a dosage of 200 mg t.i.d. Serum uric acid level was lowered by doqualast from 7.84 +/- 0.9 mg/dl to 5.09 +/- 0.8 mg/dl (p less than 0.01). Uric acid clearance increased from 7.6 +/- 2.5 ml/min to 11.5 +/- 2.4 ml/min (p less than 0.05). Excretion of uric acid in urine increased from 622 +/- 231 mg/d to 890 +/- 233 mg/d at the end of therapy. Total cholesterol in serum was lowered from 222 +/- 70 mg/dl to 159 +/- 48 mg/dl (p less than 0.05). The new uric acid lowering drug doqualast was well tolerated clinically. No adverse effects on biochemistry parameters were observed.
8名健康志愿者接受了8天的配方饮食治疗,每天额外摄入1680嘌呤碱基。从第5天开始,口服多夸司特,剂量为200毫克,每日3次。多夸司特使血清尿酸水平从7.84±0.9毫克/分升降至5.09±0.8毫克/分升(p<0.01)。尿酸清除率从7.6±2.5毫升/分钟增加到11.5±2.4毫升/分钟(p<0.05)。治疗结束时,尿中尿酸排泄量从622±231毫克/天增加到890±233毫克/天。血清总胆固醇从222±70毫克/分升降至159±48毫克/分升(p<0.05)。新型降尿酸药物多夸司特在临床上耐受性良好。未观察到对生化参数的不良反应。