Abstract:
Motor deficits observed in Parkinson’s disease (PD) are caused by the
loss of dopaminergic neurons and the subsequent dopamine depletion in different
brain areas. The most common therapy to treat motor symptoms for patients with
this disorder is the systemic intake of L- DOPA that increases dopamine levels in all
the brain, making it difficult to discern the main locus of dopaminergic action in the
alleviation of motor control. Caged compounds are molecules with the ability to
release neuromodulators locally in temporary controlled conditions using light. In the
present study, we measured the turning behavior of unilateral dopamine depleted
mice before and after dopamine uncaging. The optical delivery of dopamine in the
striatum of lesioned mice produced contralateral turning behavior that resembled, to
a lesser extent, the contralateral turning behavior evoked by a systemic injection of
apomorphine.
Contralateral turning behavior induced by dopamine uncaging was temporarily tied
to the transient elevation of dopamine concentration and was reversed when
dopamine decreased to pathological levels. Remarkably, contralateral turning
behavior was tuned by changing the power and frequency of light stimulation,
opening the possibility to modulate dopamine fluctuations using different light
stimulation protocols. Moreover, striatal dopamine uncaging recapitulated the motor
effects of a low concentration of systemic L-DOPA, but with better temporal control
of dopamine levels. Finally, dopamine uncaging reduced the pathological
synchronization of striatal neuronal ensembles that characterize unilateral
dopamine- depleted mice. We conclude that optical delivery of dopamine in the
striatum resembles the motor effects induced by systemic injection of dopaminergic
agonists in unilateral dopamine-depleted mice. Future experiments using this
approach could help to elucidate the role of dopamine in different brain nuclei in
normal and pathological conditions.