期刊论文详细信息
Diurnal variation in endothelium-dependent vasodilatation is not apparent in coronary artery disease
Article
关键词: SUDDEN CARDIAC DEATH;    C-REACTIVE PROTEIN;    CIRCADIAN VARIATION;    MYOCARDIAL-INFARCTION;    NITRIC-OXIDE;    CARDIOVASCULAR-DISEASE;    HYPERTENSIVE PATIENTS;    VASCULAR ENDOTHELIUM;    MORNING INCREASE;    UNSTABLE ANGINA;   
DOI  :  10.1161/01.CIR.103.6.806
来源: SCIE
【 摘 要 】

Background-Acute coronary syndromes present with an increased incidence from 6:00 AM to 12:00 noon. Whether endothelial function follows a diurnal rhythm and whether this rhythm is impaired in coronary artery disease (CAD) has not previously been studied. Methods and Results-Diurnal variation in endothelium-dependent vasodilatation was examined in 10 CAD patients and 10 control subjects. Forearm blood flow responses to acetylcholine, sodium nitroprusside, and N-G-monomethyl-L-arginine were determined by plethysmography at 8:00 AM, 2:00 PM, and 8:00 PM. Heart rate, blood pressure, plasma cortisol, and inflammatory markers were also determined. Heart rate and the low-frequency component of heart rate variability were greatest in the morning in control subjects, suggesting a diurnal variation in sympathetic activity. Basal forearm blood flows were significantly reduced in control subjects at 8:00 PM compared with 8:00 AM and 2:00 PM (1.2+/-0.2 versus 2.1+/-0.2 [8:00 AM] and 2.1+/-0.3 [2:00 PM] mL . 100 mL(-1) . min(-1); P<0.05) but unchanged in the CAD group. Acetylcholine (37 g/min) responses were greater at 8:00 AM than at 8:00 PM in control subjects (12.5+/-3.7 versus 19.6+/-2.9 mL . 100 mL(-1) . min(-1), respectively; P<0.05), but these responses were not time dependent in the CAD group. Responses to sodium nitroprusside were similar at all time points and between those with and without CAD. Conclusions-Thus, normal volunteers have a diurnal variation in their endothelium-dependent vasodilatation that may counteract other, potentially adverse, diurnal variations in hemodynamic and other parameters. In contrast, CAD patients who had presented with acute coronary syndromes showed a loss of this protective mechanism.

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