Dopaminergic presynaptic modulation of nigral afferents: Its role in the generation of recurrent bursting in substantia nigra pars reticulata neurons
Por:
Aceves J.J., Rueda-Orozco P.E., Hernández R., Plata V., Ibañez-Sandoval O., Galarraga E., Bargas J.
Publicada:
1 ene 2011
Resumen:
Previous work has shown the functions associated with activation of dopamine presynaptic receptors in some substantia nigra pars reticulata (SNr) afferents: (i) striatonigral terminals (direct pathway) posses presynaptic dopamine D 1-class receptors whose action is to enhance inhibitory postsynaptic currents (IPSCs) and GABA transmission. (ii) Subthalamonigral terminals posses D 1- and D 2-class receptors where D 1-class receptor activation enhances and D 2-class receptor activation decreases excitatory postsynaptic currents. Here we report that pallidonigral afferents posses D 2-class receptors (D 3 and D 4 types) that decrease inhibitory synaptic transmission via presynaptic modulation. No action of D 1-class agonists was found on pallidonigral synapses. In contrast, administration of D 1-receptor antagonists greatly decreased striatonigral IPSCs in the same preparation, suggesting that tonic dopamine levels help in maintaining the function of the striatonigral (direct) pathway. When both D 3 and D 4 type receptors were blocked, pallidonigral IPSCs increased in amplitude while striatonigral connections had no significant change, suggesting that tonic dopamine levels are repressing a powerful inhibition conveyed by pallidonigral synapses (a branch of the indirect pathway). We then blocked both D 1- and D 2-class receptors to acutely decrease direct pathway (striatonigral) and enhance indirect pathways (subthalamonigral and pallidonigral) synaptic force. The result was that most SNr projection neurons entered a recurrent bursting fringe mode similar to that observed during Parkinsonism in both patients and animal models. These results raise the question as to whether the lack of dopamine in basal ganglia output nuclei is enough to generate some pathological signs of Parkinsonism. © 2011 Aceves, Rueda-Orozco, Hernández, Plata, Ibañez-Sandoval, Galarraga and Bargas.
Filiaciones:
Aceves J.J.:
Division of Neuroscience, Institute of Cell Physiology, Universidad Nacional Autónoma de México, Distrito Federal México 04510, Mexico
Rueda-Orozco P.E.:
Division of Neuroscience, Institute of Cell Physiology, Universidad Nacional Autónoma de México, Distrito Federal México 04510, Mexico
Hernández R.:
Division of Neuroscience, Institute of Cell Physiology, Universidad Nacional Autónoma de México, Distrito Federal México 04510, Mexico
Plata V.:
Division of Neuroscience, Institute of Cell Physiology, Universidad Nacional Autónoma de México, Distrito Federal México 04510, Mexico
Ibañez-Sandoval O.:
Division of Neuroscience, Institute of Cell Physiology, Universidad Nacional Autónoma de México, Distrito Federal México 04510, Mexico
Galarraga E.:
Division of Neuroscience, Institute of Cell Physiology, Universidad Nacional Autónoma de México, Distrito Federal México 04510, Mexico
Bargas J.:
Division of Neuroscience, Institute of Cell Physiology, Universidad Nacional Autónoma de México, Distrito Federal México 04510, Mexico
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