Dopaminergic Modulation of the Striatal Microcircuit: Receptor-Specific Configuration of Cell Assemblies


Por: Carrillo-Reid, L, Hernandez-Lopez, S, Tapia, D, Galarraga, E, Bargas, J

Publicada: 19 oct 2011
Categoría: Neuroscience (miscellaneous)

Resumen:
Selection and inhibition of motor behaviors are related to the coordinated activity and compositional capabilities of striatal cell assemblies. Striatal network activity represents a main step in basal ganglia processing. The dopaminergic system differentially regulates distinct populations of striatal medium spiny neurons (MSNs) through the activation of D(1)- or D(2)-type receptors. Although postsynaptic and presynaptic actions of these receptors are clearly different in MSNs during cell-focused studies, their activation during network activity has shown inconsistent responses. Therefore, using electrophysiological techniques, functional multicell calcium imaging, and neuronal population analysis in rat corticostriatal slices, we describe the effect of selective dopaminergic receptor activation in the striatal network by observing cell assembly configurations. At the microcircuit level, during striatal network activity, the selective activation of either D(1)- or D(2)-type receptors

Filiaciones:
Carrillo-Reid, L:
 Univ Nacl Autonoma Mexico, Inst Cellular Physiol, Div Neurosci, Fac Med, Mexico City 04510, DF, Mexico

Hernandez-Lopez, S:
 Univ Nacl Autonoma Mexico, Fac Med, Dept Physiol, Mexico City 04510, DF, Mexico

Tapia, D:
 Univ Nacl Autonoma Mexico, Inst Cellular Physiol, Div Neurosci, Fac Med, Mexico City 04510, DF, Mexico

Galarraga, E:
 Univ Nacl Autonoma Mexico, Inst Cellular Physiol, Div Neurosci, Fac Med, Mexico City 04510, DF, Mexico

Bargas, J:
 Univ Nacl Autonoma Mexico, Inst Cellular Physiol, Div Neurosci, Fac Med, Mexico City 04510, DF, Mexico
ISSN: 02706474





JOURNAL OF NEUROSCIENCE
Editorial
Society for Neuroscience, 11 DUPONT CIRCLE, NW, STE 500, WASHINGTON, DC 20036 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 31 Número: 42
Páginas: 1497-1498
WOS Id: 000296274000016
ID de PubMed: 22016530

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