Circulation, Vol 72, 982-990, Copyright © 1985 by American Heart Association
J Staessen, R Fiocchi, R Bouillon, R Fagard, P Lijnen, E Moerman, A De Schaepdryver and A Amery
After 30 min rest in the lying position, 12 healthy male volunteers
(average age 22 years) received, in a randomized double-blind cross- over
protocol, either saline or naloxone (10 mg iv followed by a continuous
infusion of 10 mg/hr). Thereafter they rested for a further 30 min in the
recumbent position and for 15 min sitting on a bicycle ergometer; they then
exercised to exhaustion. At rest plasma levels of adrenocorticotropin
(ACTH), cortisol, and aldosterone increased during infusion of naloxone,
while body temperature decreased. During exercise the difference in plasma
ACTH between naloxone and saline periods was abolished, while the
differences in plasma cortisol and aldosterone lost statistical
significance. Intra-arterial pressure, heart rate, ventilation, O2 uptake,
and CO2 output were continuously monitored throughout the experiment and
were not affected by naloxone. This was also the case for several hormonal
and biochemical measurements, including those of plasma renin, angiotensin
II, norepinephrine, 13,14- dihydro-15-keto-prostaglandin F2 alpha, glucose
and lactate, and serum insulin and growth hormone. Exercise performance was
not changed by naloxone. In conclusion (1) during exhaustive graded
exercise of short duration opioidergic inhibition of the
pituitary-adrenocortical axis is probably not sustained, (2) apart from the
latter mechanism, the present study does not support the hypothesis that
endogenous opioids are involved in various hemodynamic, respiratory, and
hormonal responses to this type of exercise.
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The nature of opioid involvement in the hemodynamic respiratory and humoral responses to exercise
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