Background-Low-dose dopamine is frequently used in patients In the int
ensive care setting. Dopamine may inhibit chemoreceptor afferents and
hence decrease chemoreflex sensitivity to hypoxia, Methods and Results
-In a double-blind, randomized, crossover study, we determined the eff
ects of dopamine (5 mu g . kg(-1) . min(-1)) and placebo infusion on o
xygen saturation, minute ventilation, and sympathetic nerve activity d
uring normoxia and 5 minutes of hypoxia in 10 normal young subjects. W
e further investigated the effects of dopamine and placebo on minute v
entilation during normoxic breathing in 8 patients with severe heart f
ailure and in 8 age-matched control subjects. Dopamine did not decreas
e minute ventilation during normoxia in normal subjects. During hypoxi
a, minute ventilation was 12.9+/-1.3 L/min on dopamine and 15.8+/-1.5
L/min on placebo (P<0.0001). Oxygen saturation during hypoxia was lowe
r with dopamine (78+/-3%) than placebo (84+/-2%; P<0.0001). Sympatheti
c nerve activity during hypoxia was not enhanced with dopamine despite
the lower O-2 saturation. Subjects were able to maintain a voluntary
apnea to a lower oxygen saturation on dopamine than on placebo (P<0.05
), In heart failure patients breathing room air, but not in age-matche
d control subjects, dopamine decreased minute ventilation despite decr
eased oxygen saturation and increased PETCO2 during dopamine (all P le
ss than or equal to 0.02). Conclusions-Dopamine inhibits chemoreflex r
esponses during hypoxic breathing in normal humans, preferentially aff
ecting the ventilatory response more than the sympathetic response. Do
pamine also depresses ventilation in normoxic heart failure patients b
reathing room air. Ventilatory inhibition by low-dose dopamine may adv
ersely influence outcome in hypoxic patients, especially in patients w
ith heart failure.