Gibson T, Simmonds H A, Armstrong R D, Fairbanks L D, Rodgers A V
Br J Rheumatol. 1984 Feb;23(1):44-51. doi: 10.1093/rheumatology/23.1.44.
In a metabolic ward study of five patients, azapropazone lowered plasma uric acid but exerted only a modest and variable uricosuric effect without altering urinary xanthine and hypoxanthine levels. An alternative mechanism other than uricosuria or xanthine oxidase inhibition must account for some of the hypouricaemic action of this drug. During the first day of treatment urine volume and pH declined sharply. In a separate investigation, 22 patients were given azapropazone and 18 were given allopurinol combined with colchicine for 3 months. Allopurinol reduced plasma uric acid more quickly but at the end of the study there was little difference in the hypouricaemic results achieved by both drugs. Recurrent gout occurred more frequently with allopurinol but side-effects were confined to those taking azapropazone. A slight rise in blood urea and creatinine and a fall in haemoglobin were also features of long-term azapropazone treatment.
在一项针对5名患者的代谢病房研究中,阿扎丙宗降低了血浆尿酸水平,但仅产生了适度且变化不定的促尿酸尿作用,且未改变尿中的黄嘌呤和次黄嘌呤水平。除了促尿酸尿或抑制黄嘌呤氧化酶之外,必然存在其他机制可解释该药物的部分降尿酸作用。在治疗的第一天,尿量和尿液pH值急剧下降。在另一项研究中,22名患者服用阿扎丙宗,18名患者服用别嘌醇并联合秋水仙碱,疗程为3个月。别嘌醇降低血浆尿酸的速度更快,但在研究结束时,两种药物实现的降尿酸效果几乎没有差异。别嘌醇治疗后痛风复发更为频繁,但副作用仅出现在服用阿扎丙宗的患者中。长期服用阿扎丙宗还会导致血尿素和肌酐略有升高以及血红蛋白水平下降。