Background. Physical conditioning has been reported to increase liver oxida
tive metabolism determined by antipyrine clearance. The purpose of this inv
estigation was to study effects of aerobic conditioning on the different me
tabolic pathways of antipyrine by comparing the production clearances of an
tipyrine metabolites.
Methods. Participant: volunteers not engaged in the systematic practice of
any sport (n=14) were compared with aerobically-conditioned subjects (n=14)
Gong distance runners, defined as men running >80 km/week). Interventions:
antipyrine was administered orally. Saliva samples were collected under ba
sal conditions and at 8, 16, 24, 32 and 40 hrs following antipyrine adminis
tration. Urine was collected for 24 hrs after antipyrine ingestion.
Measures: endurance performance was expressed by the maximal oxygen uptake
((V) over dot O(2)max), the ventilatory threshold and the 4 mM.l(-1) lactat
e threshold (OBLA). Antipyrine pharmacokinetic parameters (antipyrine clear
ance and half-live) were obtained from saliva samples by the standard multi
ple-sample method.
Results. (V) over dot O(2)max, ventilatory threshold and OBLA were higher i
n trained than in control subjects (+32 %, +16% and +74%, respectively). Sa
livary antipyrine clearance was higher, whether or not this variable was co
rrected for weight (+26% and +38%, respectively), and antipyrine half-life
was significantly reduced (-31%) in runners. There was no significant chang
e with training in the renal clearance of antipyrine or in the norantipyrin
e (NORA) formation clearance but significant increases were observed in hyd
roxymethylantipyrine (HMA) and 4-hydroxyantipyrine (OHA) formation clearanc
es (+42 and +37%, respectively).
Conclusions. The findings indicate that aerobic conditioning leads to incre
ased disposition of antipyrine and that the main metabolic pathways of the
compound are changed differently.