The aim of our study was to evaluate the influence of low-intensity exercis
e on levodopa absorption and levodopa motor effect. We studied the pharmaco
kinetics and pharmacodynamics of levodopa under resting conditions and unde
r a workload of 50 watts for 2 hours on a cycle ergometer in 12 parkinsonia
n patients with predictable fluctuations of motor disability. The patients
attended the hospital on both days in a provoked off state. After a baselin
e assessment of motor disability using the Columbia University rating scale
(CURS scale) and a blood test for measurement of the baseline levodopa con
centration in the plasma, 100 mg levodopa and 25 mg benserazide were admini
stered as a single dose orally. Blood samples for measurement of the levodo
pa concentration in the plasma were taken, and motor assessments were condu
cted at 15-minute intervals for 240 minutes and at 30-minute intervals from
240 to 360 minutes. All patients were able to perform the exercise program
. The baseline Columbia University rating scale score did not differ signif
icantly between both days. The mean levodopa concentration in plasma at hal
f-maximal motor effect tended to be higher juring exercise and indicated th
at the patients needed a higher levodopa concentration in plasma to achieve
the half-maximal motor effect. The maximal levodopa concentration in plasm
a tended to be higher with exercise. Both trends did not reach statistical
significance. In summary, there was not a negative or a positive net effect
of exercise on pharmacokinetics and pharmacodynamics of levodopa. However,
there were two counteracting trends: a trend toward better levodopa absorp
tion and a trend toward a deteriorated concentration-effect correlation.