Beyer K H, Gelarden R T, Vary J E, Brown L E, Vesell E S
Department of Pharmacology, Pennsylvania State University College of Medicine, Hershey 17033.
Clin Pharmacol Ther. 1990 May;47(5):629-38. doi: 10.1038/clpt.1990.84.
In patients with azotemia, urea excretion, urea clearance, and urea/creatinine clearance ratio were increased by pyrazinoylguanidine in a dose-related manner. Urine volume and excretion of sodium greater than chloride greater than potassium tended to increase during administration of pyrazinoylguanidine. Systemic arterial pressure declined while pyrazinoylguanidine was given at 300 or 600 mg b.i.d. for 3 days. At both doses pyrazinoylguanidine reduced plasma renin activity during the first 2 hours. Between days 1 and 3 only the high dose of pyrazinoylguanidine decreased plasma renin activity and plasma aldosterone levels. These findings with pyrazinoylguanidine are consistent with those of secretion of urea in human subjects across the renal tubules and indicate that this process is susceptible to pharmacologic alteration, even in the presence of severe renal insufficiency.
在氮质血症患者中,吡嗪酰胍可使尿素排泄、尿素清除率以及尿素/肌酐清除率比值呈剂量依赖性增加。在给予吡嗪酰胍期间,尿量以及钠、氯、钾的排泄量均有增加趋势,且钠的排泄量大于氯大于钾。当给予吡嗪酰胍300或600mg,每日两次,持续3天时,体循环动脉压下降。在这两种剂量下,吡嗪酰胍在最初2小时内均降低了血浆肾素活性。仅在第1天至第3天,高剂量的吡嗪酰胍降低了血浆肾素活性和血浆醛固酮水平。吡嗪酰胍的这些发现与人类受试者肾小管尿素分泌的研究结果一致,表明即使在严重肾功能不全的情况下,这一过程也易受药物改变的影响。