Purpose: Although pyruvate supplementation enhances endurance in human
s and increases cardiac output in dogs, its effects on cardiac and per
ipheral vascular function are not known. Thus, we assessed the cardiov
ascular effects of pyruvate infusion. Materials and Methods: Aortic, l
eft ventricular (LV), and pulmonary (Ppa) pressures and LV stroke volu
me (SVlv; derived from aortic flow probe) were measured after thoracot
omy in eight anesthetized dogs. LV area or volume changes were measure
d using either an epicardial echocardiography (n = 6) or a conductance
catheter (n = 2). LV end-systolic elastance (Ees(lv)) and preload rec
ruitable stroke force (PRSF(lv)) relations, as estimates of contractil
ity, were generated by transient inferior vena cava occlusion. Simulta
neous stroke volume to arterial pressure relations during the occlusio
ns were used to measure arterial elastance (Ea), and steady-state syst
emic and pulmonary vascular resistances were used as measures of arter
ial tone. Graded doses of pyruvate (8, 16, and 32 mg/kg/min), dobutami
ne mine (positive control) and propranolol (negative control) and plac
ebo (volume control) were sequentially given. Results: Dobutamine incr
eased Ees(lv), PRSF(lv), whereas propranolol had the opposite effect o
n Ees(lv) and PRSF(lv). Pyruvate at 32 mg/kg/min increased heart rate,
Ppa, and SVlv and decreased LV end-diastolic area, and systemic vascu
lar resistance without changing arterial pressure, Ees(lv), PRSF(lv),
or Ea. Conclusions: We conclude that pyruvate infusion in normal dogs
induces venodilation but does not alter either cardiac contractility o
r arterial tone. Copyright (C) 1995 by W.B. Saunders Company