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      The role of 5-HT 2C receptors in touchscreen visual reversal learning in the rat: a cross-site study

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          Abstract

          Rationale

          Reversal learning requires associative learning and executive functioning to suppress non-adaptive responding. Reversal-learning deficits are observed in e.g. schizophrenia and obsessive-compulsive disorder and implicate neural circuitry including the orbitofrontal cortex (OFC). Serotonergic function has been strongly linked to visual reversal learning in humans and experimental animals but less is known about which receptor subtypes are involved.

          Objectives

          The objectives of the study were to test the effects of systemic and intra-OFC 5-HT 2C-receptor antagonism on visual reversal learning in rats and assess the psychological mechanisms underlying these effects within novel touchscreen paradigms.

          Methods

          In experiments 1–2, we used a novel 3-stimulus task to investigate the effects of 5-HT 2C-receptor antagonism through SB 242084 (0.1, 0.5 and 1.0 mg/kg i.p.) cross-site. Experiment 3 assessed the effects of SB 242084 in 2-choice reversal learning. In experiment 4, we validated a novel touchscreen serial visual reversal task suitable for neuropharmacological microinfusions by baclofen-/muscimol-induced OFC inactivation. In experiment 5, we tested the effect of intra-OFC SB 242084 (1.0 or 3.0 μg/side) on performance in this task.

          Results

          In experiments 1–3, SB 242084 reduced early errors but increased late errors to criterion. In experiment 5, intra-OFC SB 242084 reduced early errors without increasing late errors in a reversal paradigm validated as OFC dependent (experiment 4).

          Conclusion

          Intra-OFC 5-HT 2C-receptor antagonism decreases perseveration in novel touchscreen reversal-learning paradigms for the rat. Systemic 5-HT 2C-receptor antagonism additionally impairs late learning—a robust effect observed cross-site and potentially linked to impulsivity. These conclusions are discussed in terms of neural mechanisms underlying reversal learning and their relevance to psychiatric disorders.

          Electronic supplementary material

          The online version of this article (doi:10.1007/s00213-015-3963-5) contains supplementary material, which is available to authorized users.

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          Most cited references66

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          Abstract reward and punishment representations in the human orbitofrontal cortex.

          The orbitofrontal cortex (OFC) is implicated in emotion and emotion-related learning. Using event-related functional magnetic resonance imaging (fMRI), we measured brain activation in human subjects doing an emotion-related visual reversal-learning task in which choice of the correct stimulus led to a probabilistically determined 'monetary' reward and choice of the incorrect stimulus led to a monetary loss. Distinct areas of the OFC were activated by monetary rewards and punishments. Moreover, in these areas, we found a correlation between the magnitude of the brain activation and the magnitude of the rewards and punishments received. These findings indicate that one emotional involvement of the human orbitofrontal cortex is its representation of the magnitudes of abstract rewards and punishments, such as receiving or losing money.
            • Record: found
            • Abstract: found
            • Article: not found

            Dissociation in prefrontal cortex of affective and attentional shifts.

            The prefrontal cortex is implicated in such human characteristics as volition, planning, abstract reasoning and affect. Frontal-lobe damage can cause disinhibition such that the behaviour of a subject is guided by previously acquired responses that are inappropriate to the current situation. Here we demonstrate that disinhibition, or a loss of inhibitory control, can be selective for particular cognitive functions and that different regions of the prefrontal cortex provide inhibitory control in different aspects of cognitive processing. Thus, whereas damage to the lateral prefrontal cortex (Brodmann's area 9) in monkeys causes a loss of inhibitory control in attentional selection, damage to the orbito-frontal cortex in monkeys causes a loss of inhibitory control in 'affective' processing, thereby impairing the ability to alter behaviour in response to fluctuations in the emotional significance of stimuli. These findings not only support the view that the prefrontal cortex has multiple functions, but also provide evidence for the distribution of different cognitive functions within specific regions of prefrontal cortex.
              • Record: found
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              • Article: not found

              Cognitive inflexibility after prefrontal serotonin depletion.

              Serotonergic dysregulation within the prefrontal cortex (PFC) is implicated in many neuropsychiatric disorders, but the precise role of serotonin within the PFC is poorly understood. Using a serial discrimination reversal paradigm, we showed that upon reversal, selective serotonin depletion of the marmoset PFC produced perseverative responding to the previously rewarded stimulus without any significant effects on either retention of a discrimination learned preoperatively or acquisition of a novel discrimination postoperatively. These results highlight the importance of prefrontal serotonin in behavioral flexibility and are highly relevant to obsessive-compulsive disorder, schizophrenia, and the cognitive sequelae of drug abuse in which perseveration is prominent.

                Author and article information

                Contributors
                +44 1223 766157 , ja476@cam.ac.uk
                Journal
                Psychopharmacology (Berl)
                Psychopharmacology (Berl.)
                Psychopharmacology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0033-3158
                1432-2072
                26 May 2015
                26 May 2015
                2015
                : 232
                : 21-22
                : 4017-4031
                Affiliations
                [ ]Department of Psychology, University of Cambridge, Cambridge, CB2 3EB UK
                [ ]Behavioural and Clinical Neuroscience Institute, University of Cambridge, Cambridge, CB2 3EB UK
                [ ]Department of Neuroscience, Unit of Functional Neurobiology, University of Uppsala, Uppsala, SE-75124 Sweden
                [ ]Lilly Centre for Cognitive Neuroscience, Eli Lilly & Co. Ltd., Erl Wood Manor, Windlesham, GU20 6PH UK
                Article
                3963
                10.1007/s00213-015-3963-5
                4600472
                26007324
                f7fa5341-50bf-4f74-b997-ff180eaef08e
                © The Author(s) 2015

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 15 January 2015
                : 7 May 2015
                Categories
                Original Investigation
                Custom metadata
                © Springer-Verlag Berlin Heidelberg 2015

                Pharmacology & Pharmaceutical medicine
                reversal learning,sb 242084,5-ht2c receptor,orbitofrontal cortex,rat

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