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1.
Ann N Y Acad Sci ; 1104: 270-88, 2007 May.
Artículo en Inglés | MEDLINE | ID: mdl-17360799

RESUMEN

While extracellular dopamine (DA) concentrations are increased by a wide category of salient stimuli, there is evidence to suggest that DA responses to primary and conditioned rewards may be distinct from those elicited by other types of salient events. A reward-specific mode of neuronal responding would be necessary if DA acts to strengthen behavioral response tendencies under particular environmental conditions or to set current environmental inputs as goals that direct approach responses. As described in this review, DA critically mediates both the acquisition and expression of learned behaviors during early stages of training, however, during later stages, at least some forms of learned behavior become independent of (or less dependent upon) DA transmission for their expression.


Asunto(s)
Conducta Animal , Conducta , Dopamina/fisiología , Aprendizaje , Recompensa , Animales , Benzazepinas/farmacología , Dopamina/metabolismo , Antagonistas de Dopamina/farmacología , Electrofisiología , Humanos , Modelos Biológicos , Modelos Neurológicos , Neuronas/metabolismo , Enfermedad de Parkinson/patología , Racloprida/farmacología
2.
J Neurosci ; 23(5): 1584-7, 2003 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-12629161

RESUMEN

Previous studies have shown that D(1) receptor blockade disrupts and D(2) receptor blockade enhances long-term potentiation. These data lead to the prediction that D(1) antagonists will attenuate and D(2) antagonists will potentiate at least some types of learning. The prediction is difficult to test, however, because disruptions in either D(1) or D(2) transmission lead to reduced locomotion, exploration, and response execution and are therefore likely to impair learning that requires behavioral responding (including exploration of an environment) during the learning episode. Under a paradigm that minimizes motor requirements, rats were trained to enter a food compartment during pellet presentation. Animals then received tone-food pairings under the influence of D(1) antagonist SCH23390 (0, 0.4, 0.8, and 0.16 mg/kg) or D(2) antagonist raclopride (0, 0.2, 0.4, and 0.8 mg/kg). An additional group received unpaired presentations of tone and food. On a drug-free test day 24 hr later, animals that had been under the influence of SCH23390 (like animals that had received unpaired presentations of tone and food) showed reduced head entries in response to the tone, whereas animals that had been under the influence of raclopride showed increased head entries in response to the tone compared with vehicle controls. These data demonstrate that, under a conditioned approach paradigm, D(1) and D(2) family receptor antagonists disrupt and promote learning, respectively, as predicted by the effects of D(1) and D(2) receptor blockade on neuronal plasticity.


Asunto(s)
Conducta Apetitiva/fisiología , Condicionamiento Clásico/fisiología , Receptores de Dopamina D1/metabolismo , Receptores de Dopamina D2/metabolismo , Estimulación Acústica , Animales , Conducta Apetitiva/efectos de los fármacos , Conducta Animal/efectos de los fármacos , Conducta Animal/fisiología , Benzazepinas/farmacología , Condicionamiento Clásico/efectos de los fármacos , Antagonistas de Dopamina/farmacología , Antagonistas de los Receptores de Dopamina D2 , Aprendizaje/efectos de los fármacos , Aprendizaje/fisiología , Actividad Motora/efectos de los fármacos , Actividad Motora/fisiología , Plasticidad Neuronal/efectos de los fármacos , Plasticidad Neuronal/fisiología , Racloprida/farmacología , Ratas , Ratas Sprague-Dawley , Tiempo de Reacción/efectos de los fármacos , Receptores de Dopamina D1/antagonistas & inhibidores
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