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Treatments with losartan or enalapril are equally sensitive to deterioration in renal function from cyclooxygenase inhibition.

机译:氯沙坦或依那普利治疗对环氧合酶抑制引起的肾功能恶化同样敏感。

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摘要

Background: The beneficial effects of angiotensin converting enzyme (ACE)-inhibitors are in part mediated through the inhibition of the degradation of the vasodilator bradykinin. The bradykinin effect is counteracted by cyclooxygenase-inhibitors. Angiotensin receptor blockers (ARBs) do not affect bradykinin. Aims: To test the hypothesis that renal counteraction from a cyclooxygenase-inhibitor, diclofenac, is different in subjects treated with an ACE-inhibitor, enalapril compared with an ARB, losartan. Methods: Twelve elderly, healthy, slightly over-hydrated subjects received diclofenac orally after pre-treatment with a diuretic, bendroflumethiazide, and enalapril or bendroflumethiazide and losartan, in a double-blind cross-over fashion, with a wash-out period of at least 1 week. Results: Diclofenac reduced GFR significantly from 81(64-98) ml/min at first observations after dose for enalapril to 29(16-42) and from 76 (64-88) afler losartan to 35(24-46). There was no significant difference between enalapril and losartan in GFR. Diclofenac induced decreases in urine flow, excretion rates and clearances of sodium, osmolality clearance and free water clearance, irrespective of treatment with enalapril or losartan. However, serum potassium and handling of potassium were significantly lower after losartan-treatment. Conclusion: The negative renal effects of diclofenac administration in subjects with activation of the renin-angiotensin system and enalapril treatment are the same in subjects with activation of the renin-angiotensin system and losartan treatment.
机译:背景:血管紧张素转换酶(ACE)抑制剂的有益作用部分是通过抑制血管扩张剂缓激肽的降解而介导的。缓激肽作用被环氧合酶抑制剂抵消。血管紧张素受体阻滞剂(ARB)不会影响缓激肽。目的:为了检验以下假设:在接受ACE抑制剂依那普利治疗的受试者中,环氧合酶抑制剂双氯芬酸的肾对抗作用与氯沙坦ARB相比有所不同。方法:十二个老年,健康,水合作用过度的受试者,在双盲交叉方式下,以利尿剂,苯达氟甲酰肼,依那普利或苯达氟甲酰肼和氯沙坦预处理,口服双氯芬酸,洗净时间为。至少1周。结果:双氯芬酸将依那普利给药后的首次观察到的GFR从81(64-98)ml / min显着降低至29(16-42),从氯沙坦的76(64-88)降低至35(24-46)。依那普利和氯沙坦在GFR中无显着差异。双氯芬酸诱导的尿液流量减少,排泄率和钠清除率,重量克分子渗透浓度清除率和游离水清除率降低,而与依那普利或氯沙坦治疗无关。然而,氯沙坦治疗后,血清钾和钾的处理明显降低。结论:双氯芬酸给药对肾素-血管紧张素系统激活和依那普利治疗的受试者的肾脏负作用与肾素-血管紧张素系统激活和氯沙坦治疗的受试者相同。

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