» Articles » PMID: 33420731

Circuit Selectivity in Drug Versus Natural Reward Seeking Behaviors

Overview
Journal J Neurochem
Specialties Chemistry
Neurology
Date 2021 Jan 9
PMID 33420731
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Substance use disorder (SUD) is characterized, in part by behavior biased toward drug use and away from natural sources of reward (e.g., social interaction, food, sex). The neurobiological underpinnings of SUDs reveal distinct brain regions where neuronal activity is necessary for the manifestation of SUD-characteristic behaviors. Studies that specifically examine how these regions are involved in behaviors motivated by drug versus natural reward allow determinations of which regions are necessary for regulating seeking of both reward types, and appraisals of novel SUD therapies for off-target effects on behaviors motivated by natural reward. Here, we evaluate studies directly comparing regulatory roles for specific brain regions in drug versus natural reward. While it is clear that many regions drive behaviors motivated by all reward types, based on the literature reviewed we propose a set of interconnected regions that become necessary for behaviors motivated by drug, but not natural rewards. The circuitry is selectively necessary for drug seeking includes an Action/Reward subcircuit, comprising nucleus accumbens, ventral pallidum, and ventral tegmental area, a Prefrontal subcircuit comprising prelimbic, infralimbic, and insular cortices, a Stress subcircuit comprising the central nucleus of the amygdala and the bed nucleus of the stria terminalis, and a Diencephalon circuit including lateral hypothalamus. Evidence was mixed for nucleus accumbens shell, insular cortex, and ventral pallidum. Studies for all other brain nuclei reviewed supported a necessary role in regulating both drug and natural reward seeking. Finally, we discuss emerging strategies to further disambiguate the necessity of brain regions in drug- versus natural reward-associated behaviors.

Citing Articles

Understanding the development of a functional brain circuit: reward processing as an illustration.

Opendak M, Meyer H, Callaghan B, Abramson L, John S, Bath K Transl Psychiatry. 2025; 15(1):53.

PMID: 39962048 PMC: 11832941. DOI: 10.1038/s41398-025-03280-z.


Individual differences in prelimbic neural representation of food and cocaine seeking.

Glanzberg J, Denman A, Beacher N, Broomer M, Liang B, Li Y Cell Rep. 2024; 43(12):115022.

PMID: 39607827 PMC: 11744894. DOI: 10.1016/j.celrep.2024.115022.


Dissociable dorsal medial prefrontal cortex ensembles are necessary for cocaine seeking and fear conditioning in mice.

Liu S, Nawarawong N, Liu X, Liu Q, Olsen C Transl Psychiatry. 2024; 14(1):387.

PMID: 39313502 PMC: 11420216. DOI: 10.1038/s41398-024-03068-7.


Dynamics of human serotonin synthesis differentially link to reward anticipation and feedback.

Hahn A, Reed M, Murgas M, Vraka C, Klug S, Schmidt C Mol Psychiatry. 2024; 30(2):600-607.

PMID: 39179904 PMC: 11746133. DOI: 10.1038/s41380-024-02696-1.


Formation of an Enduring Ensemble of Accumbens Neurons Leads to Prepotent Seeking for Cocaine Over Natural Reward Cues.

Chalhoub R, Testen A, Hopkins J, Carthy C, Kalivas P bioRxiv. 2024; .

PMID: 39149274 PMC: 11326163. DOI: 10.1101/2024.08.05.606522.


References
1.
Floresco S, McLaughlin R, Haluk D . Opposing roles for the nucleus accumbens core and shell in cue-induced reinstatement of food-seeking behavior. Neuroscience. 2008; 154(3):877-84. DOI: 10.1016/j.neuroscience.2008.04.004. View

2.
Madsen H, Brown R, Short J, Lawrence A . Investigation of the neuroanatomical substrates of reward seeking following protracted abstinence in mice. J Physiol. 2012; 590(10):2427-42. PMC: 3424762. DOI: 10.1113/jphysiol.2011.225219. View

3.
Ruisoto P, Contador I . The role of stress in drug addiction. An integrative review. Physiol Behav. 2019; 202:62-68. DOI: 10.1016/j.physbeh.2019.01.022. View

4.
Mattson B, Morrell J . Preference for cocaine- versus pup-associated cues differentially activates neurons expressing either Fos or cocaine- and amphetamine-regulated transcript in lactating, maternal rodents. Neuroscience. 2005; 135(2):315-28. PMC: 1751484. DOI: 10.1016/j.neuroscience.2005.06.045. View

5.
Kruyer A, Kalivas P . Astrocytes as cellular mediators of cue reactivity in addiction. Curr Opin Pharmacol. 2020; 56:1-6. PMC: 7910316. DOI: 10.1016/j.coph.2020.07.009. View