Kd. Sumida et al., TRAINING SUPPRESSES HEPATIC LACTATE-DEHYDROGENASE ACTIVITY WITHOUT ALTERING THE ISOENZYME PROFILE, Medicine and science in sports and exercise, 27(4), 1995, pp. 507-511
A decrease in hepatic lactate dehydrogenase (LDH) activity following e
ndurance training has been a consistent observation. In the present st
udy, we sought to determine whether the training-induced decrease in h
epatic LDH activity (pyruvate = substrate) was associated with a shift
in the isoenzyme profile and/or alteration in other kinetic parameter
s. Animals (rats) were randomly assigned to either an endurance traine
d group (running 90 min at 30 m . min(-1), 10% grade) or sedentary con
trol group. Eight weeks of endurance training resulted in a significan
t decrease in maximal hepatic LDH activity for the forward reaction (p
yruvate double right arrow lactate), 107.3 +/- 5.5 mu mol . min(-1). g
(-1) when compared with control animals, 147.3 +/- 5.6 mu mol . min(-1
). g(-1) A similar decrease was observed for maximal LDH activity in t
he reverse reaction (lactate double right arrow pyruvate), 49.8 +/- 2.
1 vs 66.7 +/- 2.9 mu mol . min(-1). g(-1), trained and controls, respe
ctively. Training was also observed to decrease the Km for the reverse
reaction, 5.18 +/- 0.78 mM vs 6.94 +/- 0.55 mM, for trained and contr
ols, respectively. Km for the forward reaction was unaffected by train
ing. Gel electrophoresis with densitometric evaluation revealed no shi
ft in the isoenzyme pattern following endurance training. LDH(5) accou
nted for 89% +/- 2%, whereas 6% +/- 0.5% was observed in LDH(4), and 4
% +/- 0.3% was observed in LDH, for both groups. The densitometric are
a was similar to 34% lower from trained liver homogenates, a fractiona
l decrease similar to that observed for maximal LDH activity. The decr
ease in hepatic LDH activity with endurance training appears attributa
ble to a down regulation of enzyme content, with no significant altera
tion in isoenzyme distribution.