Cargando…
Theta oscillations in anterior cingulate cortex and orbitofrontal cortex differentially modulate accuracy and speed in flexible reward learning
Flexible reward learning relies on frontal cortex, with substantial evidence indicating that anterior cingulate cortex (ACC) and orbitofrontal cortex (OFC) subregions play important roles. Recent studies in both rat and macaque suggest theta oscillations (5–10 Hz) may be a spectral signature that co...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348740/ https://www.ncbi.nlm.nih.gov/pubmed/37456140 http://dx.doi.org/10.1093/oons/kvad005 |
_version_ | 1785073727727206400 |
---|---|
author | Ye, Tony Romero-Sosa, Juan Luis Rickard, Anne Aguirre, Claudia G. Wikenheiser, Andrew M. Blair, Hugh T. Izquierdo, Alicia |
author_facet | Ye, Tony Romero-Sosa, Juan Luis Rickard, Anne Aguirre, Claudia G. Wikenheiser, Andrew M. Blair, Hugh T. Izquierdo, Alicia |
author_sort | Ye, Tony |
collection | PubMed |
description | Flexible reward learning relies on frontal cortex, with substantial evidence indicating that anterior cingulate cortex (ACC) and orbitofrontal cortex (OFC) subregions play important roles. Recent studies in both rat and macaque suggest theta oscillations (5–10 Hz) may be a spectral signature that coordinates this learning. However, network-level interactions between ACC and OFC in flexible learning remain unclear. We investigated the learning of stimulus–reward associations using a combination of simultaneous in vivo electrophysiology in dorsal ACC and ventral OFC, partnered with bilateral inhibitory DREADDs in ACC. In freely behaving male and female rats and using a within-subject design, we examined accuracy and speed of response across distinct and precisely defined trial epochs during initial visual discrimination learning and subsequent reversal of stimulus–reward contingencies. Following ACC inhibition, there was a propensity for random responding in early reversal learning, with correct vs. incorrect trials distinguished only from OFC, not ACC, theta power differences in the reversal phase. ACC inhibition also hastened incorrect choices during reversal. This same pattern of change in accuracy and speed was not observed in viral control animals. Thus, characteristics of impaired reversal learning following ACC inhibition are poor deliberation and weak theta signaling of accuracy in this region. The present results also point to OFC theta oscillations as a prominent feature of reversal learning, unperturbed by ACC inhibition. |
format | Online Article Text |
id | pubmed-10348740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-103487402023-07-14 Theta oscillations in anterior cingulate cortex and orbitofrontal cortex differentially modulate accuracy and speed in flexible reward learning Ye, Tony Romero-Sosa, Juan Luis Rickard, Anne Aguirre, Claudia G. Wikenheiser, Andrew M. Blair, Hugh T. Izquierdo, Alicia Oxf Open Neurosci Article Flexible reward learning relies on frontal cortex, with substantial evidence indicating that anterior cingulate cortex (ACC) and orbitofrontal cortex (OFC) subregions play important roles. Recent studies in both rat and macaque suggest theta oscillations (5–10 Hz) may be a spectral signature that coordinates this learning. However, network-level interactions between ACC and OFC in flexible learning remain unclear. We investigated the learning of stimulus–reward associations using a combination of simultaneous in vivo electrophysiology in dorsal ACC and ventral OFC, partnered with bilateral inhibitory DREADDs in ACC. In freely behaving male and female rats and using a within-subject design, we examined accuracy and speed of response across distinct and precisely defined trial epochs during initial visual discrimination learning and subsequent reversal of stimulus–reward contingencies. Following ACC inhibition, there was a propensity for random responding in early reversal learning, with correct vs. incorrect trials distinguished only from OFC, not ACC, theta power differences in the reversal phase. ACC inhibition also hastened incorrect choices during reversal. This same pattern of change in accuracy and speed was not observed in viral control animals. Thus, characteristics of impaired reversal learning following ACC inhibition are poor deliberation and weak theta signaling of accuracy in this region. The present results also point to OFC theta oscillations as a prominent feature of reversal learning, unperturbed by ACC inhibition. 2023 2023-03-28 /pmc/articles/PMC10348740/ /pubmed/37456140 http://dx.doi.org/10.1093/oons/kvad005 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Ye, Tony Romero-Sosa, Juan Luis Rickard, Anne Aguirre, Claudia G. Wikenheiser, Andrew M. Blair, Hugh T. Izquierdo, Alicia Theta oscillations in anterior cingulate cortex and orbitofrontal cortex differentially modulate accuracy and speed in flexible reward learning |
title | Theta oscillations in anterior cingulate cortex and orbitofrontal cortex differentially modulate accuracy and speed in flexible reward learning |
title_full | Theta oscillations in anterior cingulate cortex and orbitofrontal cortex differentially modulate accuracy and speed in flexible reward learning |
title_fullStr | Theta oscillations in anterior cingulate cortex and orbitofrontal cortex differentially modulate accuracy and speed in flexible reward learning |
title_full_unstemmed | Theta oscillations in anterior cingulate cortex and orbitofrontal cortex differentially modulate accuracy and speed in flexible reward learning |
title_short | Theta oscillations in anterior cingulate cortex and orbitofrontal cortex differentially modulate accuracy and speed in flexible reward learning |
title_sort | theta oscillations in anterior cingulate cortex and orbitofrontal cortex differentially modulate accuracy and speed in flexible reward learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10348740/ https://www.ncbi.nlm.nih.gov/pubmed/37456140 http://dx.doi.org/10.1093/oons/kvad005 |
work_keys_str_mv | AT yetony thetaoscillationsinanteriorcingulatecortexandorbitofrontalcortexdifferentiallymodulateaccuracyandspeedinflexiblerewardlearning AT romerososajuanluis thetaoscillationsinanteriorcingulatecortexandorbitofrontalcortexdifferentiallymodulateaccuracyandspeedinflexiblerewardlearning AT rickardanne thetaoscillationsinanteriorcingulatecortexandorbitofrontalcortexdifferentiallymodulateaccuracyandspeedinflexiblerewardlearning AT aguirreclaudiag thetaoscillationsinanteriorcingulatecortexandorbitofrontalcortexdifferentiallymodulateaccuracyandspeedinflexiblerewardlearning AT wikenheiserandrewm thetaoscillationsinanteriorcingulatecortexandorbitofrontalcortexdifferentiallymodulateaccuracyandspeedinflexiblerewardlearning AT blairhught thetaoscillationsinanteriorcingulatecortexandorbitofrontalcortexdifferentiallymodulateaccuracyandspeedinflexiblerewardlearning AT izquierdoalicia thetaoscillationsinanteriorcingulatecortexandorbitofrontalcortexdifferentiallymodulateaccuracyandspeedinflexiblerewardlearning |