4.5 Article

Differential roles of medial prefrontal subregions in the regulation of drug seeking

期刊

BRAIN RESEARCH
卷 1628, 期 -, 页码 130-146

出版社

ELSEVIER
DOI: 10.1016/j.brainres.2014.12.024

关键词

Prefrontal; Frontal; Prelimbic; Infralimbic; Cortex; Addiction; Cocaine; Drugs; Cognition; Networks

资金

  1. National Institutes of Health [R21 DA032005, F31 DA035561, R01 DA006214]
  2. National Health and Medical Research Council [1072706]
  3. National Health and Medical Research Council of Australia [1072706] Funding Source: NHMRC

向作者/读者索取更多资源

The prefrontal cortex plays an important role in shaping cognition and behavior. Many studies have shown that medial prefrontal cortex (mPFC) plays a key role in seeking, extinction, and reinstatement of cocaine seeking in rodent models of relapse. Subregions of mPFC appear to play distinct roles in these behaviors, such that the prelimbic cortex (PL) is proposed to drive cocaine seeking and the infralimbic cortex (IL) is proposed to suppress cocaine seeking after extinction. This dichotomy of mPFC function may be a general attribute, as similar dorsal ventral distinctions exist for expression vs. extinction of fear conditioning. However, other results indicate that the role of mPFC neurons in reward processing is more complex than a simple PL-seek vs. IL-extinguish dichotomy. Both PL and IL have been shown to drive and inhibit drug seeking (and other types of behaviors) depending on a range of factors including the behavioral context, the drug-history of the animal, and the type of drug investigated. This heterogeneity of findings may reflect multiple subcircuits within each of these PFC areas supporting unique functions. It may also reflect the fact that the mPFC plays a multifaceted role in shaping cognition and behavior, including those overlapping with cocaine seeking and extinction. Here we discuss research leading to the hypothesis that dorsal and ventral mPFC differentially control drug seeking and extinction. We also present recent results calling the absolute nature of a PL vs. IL dichotomy into question. Finally, we consider alternate functions for mPFC that correspond less to response execution and inhibition and instead incorporate the complex cognitive behavior for which the mPFC is broadly appreciated. This article is part of a Special Issue entitled Addiction circuits. (C) 2014 Elsevier B.V. All rights reserved.

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