Among the neurodegenerative movement disorders, Parkinson's disease (PD) is the most prevalent (Schapira, 2009), affecting about 1% of people aged over 55 years, with a increase of fivefold by the age of 70, characterizing aging as the most important risk factor for this pathology (Collier et al., 2007). The first description of PD was made in 1817 by the British physician James Parkinson, who described a syndrome mainly characterized by an involuntary tremulous motion, defined as a “shaking palsy” (Parkinson, 1817). Two forms of PD have been identified: a sporadic form, which affects most than 90% of all patients and whose etiology is still unknown (Tanner, 2003), and a familial form accounting for about 10% remaining, directly linked to mutations in specific genes (Dauer and Przedborski, 2003).

The main histopathological feature of PD is the loss of dopaminergic neurons of the substantia nigra pars compacta (SNpc) (Dauer and Przedborski, 2003) with a further depletion of dopamine in the striatum. Degenerating dopaminergic neurons in PD are characterized by the presence of the accumulation of cytoplasmatic inclusions named Lewy bodies, constituted by fibrillar proteins alpha-synuclein and ubiquitin (Lees et al., 2009). Following the neuronal degeneration there is a loss of the striatal dopaminergic innervation, which ultimately results in the characteristic motor dysfunction observed in PD. In addition to the motor dysfunction, cognitive, and behavioral alterations are also observed in PD, since other neuronal groups are affected for instance in the locus coeruleus, the nucleus basalis of Meynert, and in later stages, in the neocortex (Braak et al., 2003). Although these disturbances currently do not take part in the diagnostic of PD, animal models point that they may emerge earlier than the motor disturbs (Da Cunha et al., 2001).

Though the mechanisms responsible for the loss of dopaminergic cells in PD are still unclear, there are evidences that inflammation, oxidative stress, and excitotoxicity are involved in the progression of the disease (Dawson and Dawson, 2003; Kim and Joh, 2006), albeit these events do not be specific to PD since they also contribute to other acute and chronic neurodegenerative disorders (Guimarães et al., 2009). Inflammation seems to be widely implicated to neuronal degeneration in PD because microglial cells are an important source of potentially harmful substances such as nitric oxide, free radicals, interleukin 1-beta, and tumor necrosis factor alpha (Hirsch and Hunot, 2009; Long-Smith et al., 2009).

The main dysfunctions of movement affecting PD patients are bradykinesia (slowless of movement), tremor, rigidity, postural instability, and loss of motor skills (Gelb et al., 1999). One of the treatments mostly employed to alleviate these symptoms is the administration of l-3,4-dihydroxyphenylalanine (levodopa), the dopamine precursor substance. According to Olanow et al. (2004) there are two main questions related to the action of levodopa: (1) Is it toxic? (2) Its prolonged use causes motor complications? Concerning the first point, evidences point that levodopa is toxic in cell culture (Mytilineou et al., 1993), although this had not been reported on in vivo models. Regarding the later question, Barroso-Chinea and Bezard (2010) contribute with a comprehensive review in Frontiers in Neuroanatomy. In that article the authors review the general organization of the basal ganglia and focus on the abnormal disturbance of movement developed after a continuous treatment with levodopa, termed levodopa-induced dyskinesia. This phenomenon appears to be a “side effect” of the prolonged levodopa administration, though, as pointed out by the authors, some people do not develop this disturb even after several years of levodopa treatment. Why this occurs? Even with all efforts to understand the basis of the phenomenon, it still remains unclear. This dual action of levodopa can be exemplified by the control of levels of glutamic acid decarboxylase (GAD), the enzyme of synthesis of γ-amino butyric acid (GABA), in different models of PD. While some studies report a decrease of GAD expression after administration of levodopa, others, conversely, attest an increase in its expression (Barroso-Chinea and Bezard, 2010). One hypothesis is that besides of its specific action in dopaminergic neurons, levodopa could also be involved with metabolic alterations of others neuronal groups related to motor control.

Barroso-Chinea and Bezard also highlight the efforts in the development/use of imaging techniques to study the basal ganglia, which could be employed as biomarkers to, for instance, help in an early-onset diagnosis of PD or to characterize the progression of the disease. The authors cite positron emission tomography (PET) and single photon emission computed tomography (SPECT) as tools capable of provide important information regarding the events underlying the appearing/progression of the PD. In addition, animal models reproducing neuropathological/behavioral aspects of PD also are important to a better understanding of the alterations observed during this disease.

In conclusion, more studies emphasizing not only the motor deficits but also the alterations observed in areas associative and related to cognition can provide a more comprehensive understanding of PD, especially correlated to the development of more effective drugs to reduce the disturbs observed in this pathology or even to a better understanding concerning the action of drugs already known.