Ropinirole is the first non-ergoline receptor agonist with a high, specific
affinity to the D-2 receptor family, no affinity to D-1 receptors, and onl
y a slight affinity to other neurotransmitters worldwide. Ropinirole has be
en approved for initial monotherapy of Parkinson's disease. The structure o
f this agent from the second generation of dopamine agonists is similar to
that of dopamin. Clinical studies have shown ropinirole to be highly potent
in the treatment of Parkinson's disease. The efficacy of ropinirole in ear
ly stages of the disease is comparable to that of L-dopa. Ropinirole shows
a remarkably low tendency to cause dyskinesias. Early treatment of Parkinso
n's disease with ropinirole as monotherapy delays the initiation of necessa
ry L-dopa therapy, thereby reducing long-term complications associated with
high-dosage L-dopa monotherapy. Combination therapy with ropinirole and L-
dopa facilitates maintenance therapy with low doses of L-dopa, thereby sign
ificantly reducing the L-dopa load and "off" periods as well as possible dy
skinesias induced by L-dopa treatment. The currently available clinical fin
dings on the treatment of Parkinson's disease allow the conclusion that neu
roprotection needs to be incorporated in the therapeutic concept right from
the start. The indication that ropinirole may possess neuroprotectiv prope
rties, together with its favourable safety profile, make this agent an effe
ctive dopamine agonist in the treatment of Parkinson's disease.