Cl. Oltman et al., ENDOTHELIUM-DEPENDENT VASODILATION OF PROXIMAL CORONARY-ARTERIES FROMEXERCISE-TRAINED PIGS, Journal of applied physiology, 79(1), 1995, pp. 33-40
We recently reported that alpha-adrenergic vasoconstriction is blunted
and adenosine-induced vasodilation is enhanced in proximal coronary a
rteries of exercise-trained miniature swine [C. L. Oltman, J. L. Parke
r, H. R. Adams, and M. H. Laughlin. Am. J. Physiol. 263 (Heart Circ. P
hysiol. 32): H372-H382, 1992]. The purpose of the present study was to
determine whether this model of exercise training also alters endothe
lium-dependent vasodilator responses of proximal coronary arteries. Fe
male Yucatan miniature swine were exercise trained (ET) on a motor-dri
ven treadmill or were cage confined (Sed) for 13-20 wk. Exercise toler
ance, heart weight-to-body weight ratios, and skeletal muscle oxidativ
e capacity were all significantly greater in ET than in Sed animals. V
asodilator responses were evaluated in vitro by determining concentrat
ion-response curves by using vascular rings (3.5-4 mm in axial length)
isolated from right and left coronary arteries. Vasorelaxation respon
ses were determined, after tone had been produced with either 30 mu M
prostaglandin F-2 alpha, 30 mM KCl, or 30 nM endothelin. Concentration
-response curves were obtained to endothelium-dependent vasodilators i
ncluding bradykinin (10(-9)-10(-6) M), substance P (10(-12)-10(-6) M),
clonidine (10(-9)-10(-6) M), serotonin (10(-10)-10(-5) M), and the Ca
2+ ionophore A-23187 (10(-10)-10(-6) M). Endothelium-independent vasod
ilator responses to sodium nitroprusside (10(-9)-10(-4) M) were not di
fferent between arteries from Sed and ET. Bradykinin, substance P, and
A-23187 were potent vasodilators in arteries from both groups, wherea
s serotonin and clonidine did not consistently produce vasodilation. T
here were no significant differences between the vasodilator responses
of arteries from ET and Sed pigs for any agent used in this study. We
conclude that endothelium-dependent vasodilation of proximal coronary
arteries is not altered in exercise-trained miniature swine.