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Effects of cyclooxygenase inhibition on endothelial function in hypertensive patients treated with angiotensin‐converting enzyme inhibitors
Author(s) -
Yamanari Hiroshi,
Nakamura Kazufumi,
Kakishita Mikio,
Ohe Tohru
Publication year - 2004
Publication title -
clinical cardiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.263
H-Index - 72
eISSN - 1932-8737
pISSN - 0160-9289
DOI - 10.1002/clc.4960270911
Subject(s) - medicine , aspirin , enalapril , cyclooxygenase , angiotensin converting enzyme , vasodilation , endocrinology , endothelium , ace inhibitor , prostaglandin , cyclic guanosine monophosphate , pharmacology , nitric oxide , enzyme , blood pressure , biochemistry , chemistry
Abstract Background : Cyclooxygenase inhibition restores en‐dothelium‐dependent vasodilatation in hypertension, but it is unknown whether it restores endothelial function in hypertensive patients treated with angiotensin‐converting enzyme (ACE) inhibitors. Hypothesis : The purpose of the present study was to evaluate the effects of cyclooxygenase inhibition on endothelial function in hypertensive patients treated with ACE inhibitors. Methods : Endothelium‐dependent flow‐mediated dilatation (FMD) and endothelium‐independent glyceryl trinitrate‐induced dilatation were investigated in 10 patients treated with enalapril (ACE group), 11 patients treated with manidipine and metoprolol (non‐ACE group), and 12 normotensive control subjects. After administration of 1000 mg of aspirin, FMD was investigated once again. Plasma cyclic guanosine monophos‐phate (cGMP) and eicosanoids were also measured during reactive hyperemia before and after aspirin administration. Results : Flow‐mediated dilatation was more impaired in the non‐ACE group than in the ACE group (8.3 ± 3.8%, 5.7 ± 1.7%, respectively, p<0.04). Glyceryl trinitrate‐induced dilatation was similar in the ACE group, the non‐ACE group, and in the control subjects. In the ACE group, FMD was reduced after administration of aspirin (5.3 ± 4.2%, p<0.05). The percent change in FMD after administration of aspirin correlated significantly with percent change in cGMP (r = 0.77, p<0.03; y‐intercept, −62.1%, p<0.01). After aspirin administration, levels of thromboxane B2 and 6‐keto‐prosta‐glandiniα were significantly decreased compared with those before aspirin administration in all groups. Conclusions : Cyclooxygenase inhibition may reduce the beneficial effect on endothelium‐dependent vasodilatation induced by ACE inhibitors. The results suggested that prostacy‐clin in addition to nitric oxide plays a significant role in the restoration of endothelial function in hypertensive patients treated with ACE inhibitors.

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