Trnavský K, Rovenský J
Pharmacology. 1976;14(4):378-84. doi: 10.1159/000136618.
In experiments with rats, the influence of the treatment with sodium salicylate (350 mg/kg), phenylbutazone (100 mg/kg), cyclophosphamide (5 mg/kg), 6-mercaptopurine (25 mg/kg) and D-penicillamine (50 mg/kg), on urinary lactate dehydrogenase, leucine aminopeptidase and alanine aminopeptidase was investigated. All these drugs caused an increase in the enzyme levels in urine. In the case of sodium salicylate, the increase occurred only after the first administration of the drug; phenylbutazone caused a gradual increase of the enzymes. Cytostatic drugs caused an increase in the level of the investigated enzymes in urine with a maximum after 1 week of treatment.
在对大鼠进行的实验中,研究了水杨酸钠(350毫克/千克)、保泰松(100毫克/千克)、环磷酰胺(5毫克/千克)、6-巯基嘌呤(25毫克/千克)和D-青霉胺(50毫克/千克)处理对尿乳酸脱氢酶、亮氨酸氨肽酶和丙氨酸氨肽酶的影响。所有这些药物均导致尿中酶水平升高。就水杨酸钠而言,仅在首次给药后酶水平出现升高;保泰松导致酶水平逐渐升高。细胞毒性药物使尿中所研究酶的水平升高,在治疗1周后达到最高值。