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氯沙坦或依那普利治疗对环氧化酶抑制导致的肾功能恶化同样敏感。

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

作者信息

Juhlin Tord, Erhardt Leif R, Ottosson Helene, Jönsson Bo A G, Höglund Peter

机构信息

Department of Cardiology, Malmö University Hospital, Malmö, Sweden.

出版信息

Eur J Heart Fail. 2007 Feb;9(2):191-6. doi: 10.1016/j.ejheart.2006.05.015. Epub 2006 Jul 20.

Abstract

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) after 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.

摘要

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舒张剂缓激肽的降解来介导的。环氧化酶抑制剂可抵消缓激肽的作用。血管紧张素受体阻滞剂(ARB)不影响缓激肽。

目的

检验以下假设:与使用ARB氯沙坦治疗的受试者相比,使用ACE抑制剂依那普利治疗的受试者中,环氧化酶抑制剂双氯芬酸的肾脏拮抗作用有所不同。

方法

12名老年、健康、轻度水合过度的受试者,在预先使用利尿剂苄氟噻嗪和依那普利或苄氟噻嗪和氯沙坦进行预处理后,以双盲交叉方式口服双氯芬酸,洗脱期至少为1周。

结果

双氯芬酸使依那普利给药后首次观察时的肾小球滤过率(GFR)从81(64 - 98)ml/min显著降至29(16 - 42),使氯沙坦给药后的GFR从76(64 - 88)降至35(24 - 46)。依那普利和氯沙坦在GFR方面无显著差异。无论使用依那普利还是氯沙坦治疗,双氯芬酸均可导致尿流量、钠排泄率和清除率、渗透清除率和自由水清除率降低。然而,氯沙坦治疗后血清钾及钾的处理显著降低。

结论

在肾素 - 血管紧张素系统激活且接受依那普利治疗的受试者中,双氯芬酸给药的负面肾脏效应与肾素 - 血管紧张素系统激活且接受氯沙坦治疗的受试者相同。

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