Literature DB >> 22219222

The selective serotonin reuptake inhibitor, escitalopram, enhances inhibition of prepotent responding and spatial reversal learning.

Holden D Brown1, Dionisio A Amodeo, John A Sweeney, Michael E Ragozzino.   

Abstract

Previous findings indicate treatment with a selective serotonin reuptake inhibitor (SSRI) facilitates behavioral flexibility when conditions require inhibition of a learned response pattern. The present experiment investigated whether acute treatment with the SSRI, escitalopram, affects behavioral flexibility when conditions require inhibition of a naturally biased response pattern (elevated conflict test) and/or reversal of a learned response pattern (spatial reversal learning). An additional experiment was carried out to determine whether escitalopram, at doses that affected behavioral flexibility, also reduced anxiety as tested in the elevated plus-maze. In each experiment, Long-Evans rats received an intraperitoneal injection of either saline or escitalopram (0.03, 0.3 or 1.0 mg/kg) 30 min prior to behavioral testing. Escitalopram, at all doses tested, enhanced acquisition in the elevated conflict test, but did not affect performance in the elevated plus-maze. Escitalopram (0.3 and 1.0 mg/kg) did not alter acquisition of the spatial discrimination, but facilitated reversal learning. In the elevated conflict and spatial reversal learning test, escitalopram enhanced the ability to maintain the relevant strategy after being initially selected. The present findings suggest that enhancing serotonin transmission with an SSRI facilitates inhibitory processes when conditions require a shift away from either a naturally biased response pattern or a learned choice pattern.

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Year:  2012        PMID: 22219222      PMCID: PMC3345307          DOI: 10.1177/0269881111430749

Source DB:  PubMed          Journal:  J Psychopharmacol        ISSN: 0269-8811            Impact factor:   4.153


  79 in total

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Journal:  J Neurosci       Date:  2010-12-15       Impact factor: 6.167

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5.  Short- and long-term memory are differentially regulated by monoaminergic systems in the rat brain.

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6.  Serotonin and substance P afferents to parafascicular and central medial nuclei.

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  16 in total

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2.  Maternal immune activation impairs cognitive flexibility and alters transcription in frontal cortex.

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3.  Cognitive set shifting deficits and their relationship to repetitive behaviors in autism spectrum disorder.

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Journal:  J Autism Dev Disord       Date:  2015-03

4.  Sequential reversal learning: a new touchscreen schedule for assessing cognitive flexibility in mice.

Authors:  Anna U Odland; Rune Sandahl; Jesper T Andreasen
Journal:  Psychopharmacology (Berl)       Date:  2020-10-30       Impact factor: 4.530

5.  Reduced behavioral flexibility in autism spectrum disorders.

Authors:  Anna-Maria D'Cruz; Michael E Ragozzino; Matthew W Mosconi; Sunil Shrestha; Edwin H Cook; John A Sweeney
Journal:  Neuropsychology       Date:  2013-03       Impact factor: 3.295

Review 6.  The neural basis of reversal learning: An updated perspective.

Authors:  A Izquierdo; J L Brigman; A K Radke; P H Rudebeck; A Holmes
Journal:  Neuroscience       Date:  2016-03-12       Impact factor: 3.590

7.  Pedunculopontine tegmental nucleus lesions impair probabilistic reversal learning by reducing sensitivity to positive reward feedback.

Authors:  Anam Syed; Phillip M Baker; Michael E Ragozzino
Journal:  Neurobiol Learn Mem       Date:  2016-03-11       Impact factor: 2.877

8.  Cognitive flexibility impairment and reduced frontal cortex BDNF expression in the ouabain model of mania.

Authors:  Dionisio A Amodeo; Gena Grospe; Hui Zang; Yogesh Dwivedi; Michael E Ragozzino
Journal:  Neuroscience       Date:  2016-06-04       Impact factor: 3.590

9.  Risperidone and the 5-HT2A receptor antagonist M100907 improve probabilistic reversal learning in BTBR T + tf/J mice.

Authors:  Dionisio A Amodeo; Joshua H Jones; John A Sweeney; Michael E Ragozzino
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Review 10.  Using mice to model Obsessive Compulsive Disorder: From genes to circuits.

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