New medications recently developed for treating Parkinson's disease in
clude two inhibitors of catechol-O-methyltransferase (COMT), entacapon
e and tolcapone, which, by decreasing the elimination of levodopa, ext
end the duration of its effects. Increased 'on' rime and less 'wearing
-off' symptomatology can be expected with the use of these COMT inhibi
tors. Two non-ergot dopaminergic agonists (pramipexole and ropinirole)
and a long-acting ergoline (cabergoline) are also being introduced. T
hese dopaminergic agonists, like the ergot derivatives currently avail
able (bromocriptine, lisuride, and pergolide), are useful as adjuncts
to levodopa, and are also efficacious as monotherapies.