Effect of Allopurinol Administration on the Prevention of Muscle Mass Loss in Subject Immobilized.
Status:
Completed
Trial end date:
2016-07-01
Target enrollment:
Participant gender:
Summary
Generating critical levels of power is a prerequisite for performing simple daily activities,
such as rising from a chair or climbing stairs. For a young healthy person these activities
can be performed easily, however after a prolonged period of forced inactivity (such as
during the recovery from a sports injury, prolonged bed rest or spaceflight) a loss of muscle
mass occurs. It has been suggested that this loss may be triggered by oxidative stress. An
enzyme involved in the production of free radicals in various experimental models, including
immobilization, is xanthine oxidase (XO). Although allopurinol is an inhibitor of XO widely
used in clinical practice, its effect on the maintenance of muscle mass after an
immobilization protocol is unknown. Thus, the major aim of this clinical trial is to
determine the effect of allopurinol administration on the prevention of muscle mass loss in
immobilized subjects.
This is a prospective, randomized study in which fifty young male subjects (aged between 25
and 40 years) diagnosed with grade II ankle sprain will be recruited. After immobilization
the patients will be assigned randomly to one of two experimental groups, one treated with
allopurinol (n=25) and the other with placebo (n=25). The dosage of allopurinol will be the
same as recommended for gout patients, i.e. 300 mg/day orally, during all the immobilization
period, which will last fifteen days. This medication will be delivered to the patients when
they agree to participate in the clinical trial. They will be immobilized by posterior knee
splint, preventing use of that leg.
We will determine muscle mass loss by performing two magnetic resonances of both legs before
and after the immobilization period. We will also take two blood samples (before and after
immobilization) to measure oxidative stress parameters (malondialdehyde, protein carbonyls,
and XO activity), inflammatory parameters (IL-6, C-reactive protein and 1-antichymotrypsin),
as well as vitamin D levels.