ENDOTHELIN IN CORONARY ENDOTHELIAL DYSFUNCTION AND EARLY ATHEROSCLEROSIS IN HUMANS

被引:311
作者
LERMAN, A
HOLMES, DR
BELL, MR
GARRATT, KN
NISHIMURA, RA
BURNETT, JC
机构
[1] Div. Cardiovasc. Dis. and Int. Med., Mayo Clinic/Foundation, Rochester, MN
[2] Div. Cardiovasc. Dis. and Int. Med., Mayo Clinic, Rochester, MN 55905
关键词
ENDOTHELIUM; ENDOTHELIN; ACETYLCHOLINE GUANOSINE;
D O I
10.1161/01.CIR.92.9.2426
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The endothelium modulates vascular lone through release of vasodilating substances, such as endothelium-derived relaxing factors, and vasoconstricting substances, such as endothelin. Endothelin concentrations are elevated in humans with atherosclerosis and in hypercholesterolemic pigs. Furthermore, the endothelium-dependent vasodilator acetylcholine increases endothelin in hypercholesterolemia in association with coronary vasoconstriction. The present study was designed to test the hypotheses that coronary endothelial dysfunction in humans is characterized by enhanced coronary and circulating endothelin and that the vasoconstriction associated with acetylcholine results in further release of coronary endothelin. Methods and Results Coronary and circulating endothelin concentrations were measured at baseline and during intracoronary acetylcholine administration in 20 patients undergoing diagnostic coronary angiography. Patients were divided into two groups on the basis of their response to intracoronary acetylcholine. Group 1 (n=7) demonstrated a normal vasodilatory response, but group 2 (n=13) demonstrated coronary vasoconstriction. Baseline coronary and circulating endothelin concentrations (as determined by coronary sinus and femoral artery measurements, respectively) were higher in patients who responded to acetylcholine with coronary vasoconstriction (group 2) than in group 1 patients (coronary sinus, 15.9+/-1.0 pg/mL versus 7.1+/-1.0 pg/mL; femoral, 14.1+/-0.9 pg/mL versus 6.8+/-1.0 pg/mL, respectively; P<.01). rn response to intracoronary acetylcholine, a further increase in coronary endothelin was observed only in group 2; this increase correlated with changes in coronary artery diameter. Conclusions This study demonstrates that endothelin immunoreactivity is enhanced in the coronary and systemic circulation in humans with coronary endothelial dysfunction. Moreover, acetylcholine further increased coronary endothelin concentration in patients with coronary endothelial dysfunction and was associated with coronary vasoconstriction. These observations strongly support a role for endothelin as an early participant in and marker for coronary endothelial dysfunction in humans.
引用
收藏
页码:2426 / 2431
页数:6
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