Jungmann E, Seel K, Hofmann E, Scheuermann E H, Schöffling K
Zentrum der Inneren Medizin, Johann Wolfgang Goethe-Universität Frankfurt am Main.
Klin Wochenschr. 1989 Dec 4;67(23):1174-81. doi: 10.1007/BF01716204.
We examined renal responses to a pharmacological dosage of human atrial natriuretic peptide (hANP) and the potential interference of nifedipine administration with the effects of hANP on kidney function in healthy subjects and normoglycemic patients with type 1 diabetes mellitus. Ten healthy volunteers (age, 28 +/- 1 years) and ten patients (age, 33 +/- 2 years; diabetes duration; 14 +/- 3 years; HbAI 7.2% +/- 0.2%) were studied. According to a double-blind, randomized, placebo-controlled trial design, three experiments were performed in each subject using the double-dummy technique: placebo only, hANP only, and nifedipine + hANP. As i.v. bolus injection 100 micrograms hANP was given; nifedipine was applied buccally, at a dose of 10 mg 90 min before and at a dose of 5 mg together with hANP injection. At base-line and in the placebo only experiment, patients did not differ from controls. In the hANP only experiment, in both groups hANP resulted in increased urinary volume and both sodium and chloride excretion (P less than 0.05 vs placebo only experiment). In patients, hANP-induced increase in electrolyte excretion was greater than in controls (P less than 0.05). In the nifedipine + hANP experiment, hANP-induced changes in renal indexes were enhanced in controls (P less than 0.05 vs hANP only experiment) but not in patients. Thus, diuretic response to nifedipine + hANP in patients was decreased in comparison with controls (P less than 0.05). In patients, however, nifedipine administration decreased the hANP-induced increase in urinary albumin excretion (P less than 0.05 vs hANP only experiment). Creatinine clearance was uninfluenced throughout the experiments.(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究了健康受试者以及血糖正常的1型糖尿病患者对药理学剂量的人心房利钠肽(hANP)的肾脏反应,以及硝苯地平给药对hANP肾脏功能效应的潜在干扰。研究了10名健康志愿者(年龄28±1岁)和10名患者(年龄33±2岁;糖尿病病程14±3年;糖化血红蛋白7.2%±0.2%)。根据双盲、随机、安慰剂对照试验设计,采用双模拟技术在每个受试者身上进行了三个实验:仅安慰剂、仅hANP、硝苯地平+hANP。静脉推注给予100微克hANP;硝苯地平经口腔给药,在hANP注射前90分钟给予10毫克剂量,与hANP注射同时给予5毫克剂量。在基线和仅安慰剂实验中,患者与对照组无差异。在仅hANP实验中,两组中hANP均导致尿量增加以及钠和氯排泄增加(与仅安慰剂实验相比,P<0.05)。在患者中,hANP诱导的电解质排泄增加大于对照组(P<0.05)。在硝苯地平+hANP实验中,hANP诱导的肾脏指标变化在对照组中增强(与仅hANP实验相比,P<0.05),但在患者中未增强。因此,与对照组相比,患者对硝苯地平+hANP的利尿反应降低(P<0.05)。然而,在患者中,硝苯地平给药降低了hANP诱导的尿白蛋白排泄增加(与仅hANP实验相比,P<0.05)。整个实验过程中肌酐清除率未受影响。(摘要截断于250字)