» Articles » PMID: 25673861

Prospective Coding of Dorsal Raphe Reward Signals by the Orbitofrontal Cortex

Overview
Journal J Neurosci
Specialty Neurology
Date 2015 Feb 13
PMID 25673861
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

The orbitofrontal cortex (OFC) is important for the cognitive processes of learning and decision making. Previous recordings have revealed that OFC neurons encode predictions of reward outcomes. The OFC is interconnected with the dorsal raphe nucleus (DRN), which is a major serotonin (5-HT) center of the brain. Recent studies have provided increasing evidence that the DRN encodes reward signals. However, it remains unclear how the activity of DRN neurons affects the prospective reward coding of OFC neurons. By combining single-unit recordings from the OFC and optogenetic activation of the DRN in behaving mice, we found that DRN stimulation is sufficient to organize and modulate the anticipatory responses of OFC neurons. During pavlovian conditioning tasks for mice, odorant cues were associated with the delayed delivery of natural rewards of sucrose solution or DRN stimulation. After training, OFC neurons exhibited prospective responses to the sucrose solution. More importantly, the coupling of an odorant with delayed DRN stimulation resulted in tonic excitation or inhibition of OFC neurons during the delay period. The intensity of the prospective responses was affected by the frequency and duration of DRN stimulation. Additionally, DRN stimulation bidirectionally modulated the prospective responses to natural rewards. These experiments indicate that signals from the DRN are incorporated into the brain reward system to shape the cortical prospective coding of rewards.

Citing Articles

Prefrontal Cortex subregions provide distinct visual and behavioral feedback modulation to the Primary Visual Cortex.

Ahrlund-Richter S, Osako Y, Jenks K, Odom E, Huang H, Arnold D bioRxiv. 2024; .

PMID: 39149348 PMC: 11326267. DOI: 10.1101/2024.08.06.606894.


Striatal Serotonin Release Signals Reward Value.

Spring M, Nautiyal K J Neurosci. 2024; 44(41).

PMID: 39117457 PMC: 11466065. DOI: 10.1523/JNEUROSCI.0602-24.2024.


A Role for Serotonin in Modulating Opposing Drive and Brake Circuits of Impulsivity.

Desrochers S, Spring M, Nautiyal K Front Behav Neurosci. 2022; 16:791749.

PMID: 35250501 PMC: 8892181. DOI: 10.3389/fnbeh.2022.791749.


Prospective representations in rat orbitofrontal ensembles.

Zhou J, Zong W, Jia C, Gardner M, Schoenbaum G Behav Neurosci. 2021; 135(4):518-527.

PMID: 34165997 PMC: 9344202. DOI: 10.1037/bne0000451.


A single dose of escitalopram blunts the neural response in the thalamus and caudate during monetary loss.

Lewis C, Mueller K, Zsido R, Reinelt J, Regenthal R, Okon-Singer H J Psychiatry Neurosci. 2021; 46(3):E319-E327.

PMID: 33904667 PMC: 8327975. DOI: 10.1503/jpn.200121.


References
1.
Schoenbaum G, Chiba A, Gallagher M . Orbitofrontal cortex and basolateral amygdala encode expected outcomes during learning. Nat Neurosci. 1999; 1(2):155-9. DOI: 10.1038/407. View

2.
Tremblay L, Schultz W . Relative reward preference in primate orbitofrontal cortex. Nature. 1999; 398(6729):704-8. DOI: 10.1038/19525. View

3.
Cavada C, Company T, Tejedor J, Cruz-Rizzolo R, Reinoso-Suarez F . The anatomical connections of the macaque monkey orbitofrontal cortex. A review. Cereb Cortex. 2000; 10(3):220-42. DOI: 10.1093/cercor/10.3.220. View

4.
Bechara A, Damasio H, Damasio A . Emotion, decision making and the orbitofrontal cortex. Cereb Cortex. 2000; 10(3):295-307. DOI: 10.1093/cercor/10.3.295. View

5.
Millan M . Improving the treatment of schizophrenia: focus on serotonin (5-HT)(1A) receptors. J Pharmacol Exp Ther. 2000; 295(3):853-61. View