» Articles » PMID: 20153781

Selective Lesions of the Dorsomedial Striatum Impair Serial Spatial Reversal Learning in Rats

Overview
Journal Behav Brain Res
Date 2010 Feb 16
PMID 20153781
Citations 89
Authors
Affiliations
Soon will be listed here.
Abstract

Impairments in reversal learning have been attributed to orbitofrontal cortex (OFC) dysfunction in many species. However, the role of subcortical areas interconnected with the OFC such as the striatum remains poorly understood. This study directly evaluated the contribution of core and shell sub-regions of the nucleus accumbens (NAc), dorsomedial (DMS) and dorsolateral (DLS) striatum to reversal learning of an instrumental two-lever spatial discrimination task in rats. Selective NAc core, DMS and DLS lesions were achieved with microinjections of quinolinic acid and NAc shell lesions with ibotenic acid. Damage to NAc core or shell did not affect retention of a previously acquired instrumental spatial discrimination. In contrast, DLS and DMS lesions produced changes in aspects of discrimination performance such as the latency to collect earned food pellets. Neither NAc core or shell lesions nor DLS lesions affected the main indices of reversal performance. Conversely, DMS lesion rats showed a significant impairment in reversal learning. DMS damage increased the number of errors to reach criteria that were perseverative in nature. The deficit in reversal learning in DMS lesion rats was not associated with an impairment to extinguish instrumental responding. There were no effects on spontaneous locomotor activity. Our data are in agreement with recent work showing that lesions of the medial striatum in marmoset monkeys produce perseverative impairments during a serial visual discrimination reversal task and support the hypothesis that dorsomedial striatal dysfunction contributes to pathological perseveration, which is a common feature of many psychiatric disorders.

Citing Articles

Assessing cognitive flexibility in mice using a custom-built touchscreen chamber.

Pais R, Goldani A, Hutchison J, Mazrouei A, Khavaninzadeh M, Molina L Front Behav Neurosci. 2025; 19:1536458.

PMID: 40017733 PMC: 11865062. DOI: 10.3389/fnbeh.2025.1536458.


The Aggregation of -Synuclein in the Dorsomedial Striatum Significantly Impairs Cognitive Flexibility in Parkinson's Disease Mice.

Chen J, Liu Y, Su M, Sun Y, Liu C, Sun S Biomedicines. 2024; 12(8).

PMID: 39200099 PMC: 11351470. DOI: 10.3390/biomedicines12081634.


Postnatal Phencyclidine-Induced Deficits in Decision Making Are Ameliorated by Optogenetic Inhibition of Ventromedial Orbitofrontal Cortical Glutamate Neurons.

Tranter M, Faget L, Hnasko T, Powell S, Dillon D, Barnes S Biol Psychiatry Glob Open Sci. 2024; 4(1):264-274.

PMID: 38298783 PMC: 10829674. DOI: 10.1016/j.bpsgos.2023.08.002.


Dissociating the contributions of sensorimotor striatum to automatic and visually guided motor sequences.

Mizes K, Lindsey J, Escola G, Olveczky B Nat Neurosci. 2023; 26(10):1791-1804.

PMID: 37667040 PMC: 11187818. DOI: 10.1038/s41593-023-01431-3.


Enhancing reinforcement learning models by including direct and indirect pathways improves performance on striatal dependent tasks.

Blackwell K, Doya K PLoS Comput Biol. 2023; 19(8):e1011385.

PMID: 37594982 PMC: 10479916. DOI: 10.1371/journal.pcbi.1011385.


References
1.
Cools R, Lewis S, Clark L, Barker R, Robbins T . L-DOPA disrupts activity in the nucleus accumbens during reversal learning in Parkinson's disease. Neuropsychopharmacology. 2006; 32(1):180-9. DOI: 10.1038/sj.npp.1301153. View

2.
Floresco S, Ghods-Sharifi S, Vexelman C, Magyar O . Dissociable roles for the nucleus accumbens core and shell in regulating set shifting. J Neurosci. 2006; 26(9):2449-57. PMC: 6793649. DOI: 10.1523/JNEUROSCI.4431-05.2006. View

3.
Boulougouris V, Dalley J, Robbins T . Effects of orbitofrontal, infralimbic and prelimbic cortical lesions on serial spatial reversal learning in the rat. Behav Brain Res. 2007; 179(2):219-28. DOI: 10.1016/j.bbr.2007.02.005. View

4.
Ragozzino M, Detrick S, Kesner R . Involvement of the prelimbic-infralimbic areas of the rodent prefrontal cortex in behavioral flexibility for place and response learning. J Neurosci. 1999; 19(11):4585-94. PMC: 6782617. View

5.
Balleine B, Liljeholm M, Ostlund S . The integrative function of the basal ganglia in instrumental conditioning. Behav Brain Res. 2008; 199(1):43-52. DOI: 10.1016/j.bbr.2008.10.034. View