Abstract

Studies on prefrontal cortex (PFC) dopamine (DA) function have revealed its essential role in mediating a variety of cognitive and executive functions. A general principle that has emerged (primarily from studies on working memory) is that PFC DA, acting on D1 receptors, regulates cognition in accordance to an “inverted-U” shaped function, so that too little or too much activity has detrimental effects on performance. However, contemporary studies have indicated that the receptor mechanisms through which mesocortical DA regulates different aspects of behavioral flexibility can vary considerably across different DA receptors and cognitive operations. This article will review psychopharmacological and neurochemical data comparing and contrasting the cognitive effects of antagonism and stimulation of different DA receptors in the medial PFC. Thus, set-shifting is dependent on a co-operative interaction between PFC D1 and D2 receptors, yet, supranormal stimulation of these receptors does not appear to have detrimental effects on this function. On the other hand, modification of cost/benefit decision biases in situations involving reward uncertainty is regulated in complex and sometimes opposing ways by PFC D1 vs. D2 receptors. When viewed collectively, these findings suggest that the “inverted-U” shaped dose-response curve underlying D1 receptor modulation of working memory is not a one-size-fits-all function. Rather, it appears that mesocortical DA exerts its effects via a family of functions, wherein reduced or excessive DA activity can have a variety of effects across different cognitive domains.

Highlights

  • Studies on prefrontal cortex (PFC) dopamine (DA) function have revealed its essential role in mediating a variety of cognitive and executive functions

  • The notion that normal PFC functioning is dependent on an optimum range of DA activity, whereas “too little” or “too much” D1 receptor stimulation has detrimental effects on working memory has become a cornerstone of our understanding of how mesocortical DA regulates cognition

  • Expression of D1 receptors on principle pyramidal neurons appears to be substantially greater than D2 receptors (Gaspar et al, 1995), whereas both types of receptors have been localized on GABAergic interneurons and may reside on presynaptic excitatory glutamate terminals (Sesack et al, 1995; Mrzijak et al, 1996; Muly et al, 1998; Wedzony et al, 2001)

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Summary

Introduction

Studies on prefrontal cortex (PFC) dopamine (DA) function have revealed its essential role in mediating a variety of cognitive and executive functions. The fact that blockade of DA receptors in the rat medial PFC did not impair delayed alternation suggests that this form of delayed responding is not a sensitive paradigm for assessing PFC DA regulation of working memory functions in rodents.

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