Summary: Cocaine and sucrose neuron ensembles in the nucleus accumbens are mostly non-overlapping.
Source: University of Wyoming
Nucleus accumbens in the brain play a central role in the risk-reward circuit. Their operation is based chiefly on three essential neurotransmitters: dopamine, which promotes desire; serotonin, whose effects include satiety and inhibition; and glutamate, which drives goal-directed behaviors and responses to reward-associated cues and contexts.
In a study using genetically modified mice, a University of Wyoming faculty member found that the nucleus accumbens ensembles recruited by cocaine use are largely distinct from nucleus accumbens ensembles recruited by sucrose, or table sugar. Because they are separate, this poses the possibility that drug use can be addressed without affecting biologically adaptive seeking of reward.
“We established that, in the nucleus accumbens, a key brain region of reward processing, the neuronal ensembles — a sparse network of neurons activated simultaneously — are reward-specific, and sucrose and cocaine ensembles are mostly nonoverlapping,” says Ana Clara Bobadilla, a UW assistant professor in the School of Pharmacy and in the WWAMI (Washington, Wyoming, Alaska, Montana and Idaho) Medical Education Program.
Bobadilla is lead author of a paper, titled “Cocaine and Sucrose Rewards Recruit Different Seeking Ensembles in the Nucleus Accumbens Core,” that was published in the Sept. 28 issue of Molecular Psychiatry. The journal publishes work aimed at elucidating biological mechanisms underlying psychiatric disorders and their treatment. The emphasis is on studies at the interface of pre-clinical and clinical research, including studies at the cellular, molecular, integrative, clinical, imaging and psychopharmacology levels.
Bobadilla conducted the research while completing her postdoctoral work at the Medical University of South Carolina. The project began in mid-2017. One contributor to the study is now working at the University of Colorado Anschutz Medical Campus.
Currently, the recruitment process within each reward-specific ensemble is unknown, she says. However, using molecular biology tools, Bobadilla was able to identify what type of cells was recruited in both the cocaine and sucrose ensemble.
These cells are known as GABAergic projection neurons, also called medium spiny neurons. They comprise 90 percent to 95 percent of the neuronal population with the nucleus accumbens. These medium spiny neurons express the dopamine D1 or D2 receptor.
The study determined the sucrose and cocaine ensembles recruited mostly D1 receptor expressing medium spiny neurons. These results are in line with the general understanding in the field that activation of the D1 pathway promotes reward seeking, while D2 pathway activation can lead to aversion or reduced seeking, Bobadilla says.
“In humans, drugs are rarely used in the vacuum. Most of us have complex lives including lots of sources of nondrug rewards, such as food, water, social interaction or sex,” Bobadilla explains. “Like drugs, these rewards drive and influence our behavior constantly. The dual cocaine and sucrose model used in this study allows us to characterize the cocaine-specific ensemble after the mice experienced sucrose, another type of competing reward.
“It is a more complex model, but one that is closer to what occurs in people suffering from substance use disorders, who fight competing rewards daily,” she adds.
Bobadilla is now focused on the question of how cells are recruited in ensembles. Additionally, she aims to address another fundamental question in addiction research: whether the same network-specific mechanisms underlie the seeking of all drug rewards.
“All drugs of abuse share high probability of relapse,” she says. “However, each class of addictive drug displays different acute pharmacology and synaptic plasticity. We are now investigating if reward-specific properties of ensembles can explain these differences.”
Funding: The study was funded, in part, by Bobadilla’s postdoctoral mentor, Peter Kalivas, a professor and chair of neuroscience at the Medical University of South Carolina, and by a National Institutes of Health Pathway to Independence Award Bobadilla obtained in early 2019.
About this neuroscience research news
Source: University of Wyoming Contact: Ana Clara Bobadilla – University of Wyoming Image: The image is in the public domain
Cocaine and sucrose rewards recruit different seeking ensembles in the nucleus accumbens core
Poorly regulated reward seeking is a central feature of substance use disorder. Recent research shows that rewarding drug-related experiences induce synchronous activation of a discrete number of neurons in the nucleus accumbens that are causally linked to reward-related contexts. Here we comprehensively characterize the specific ensemble of neurons built through experience that are linked to seeking behavior. We additionally address the question of whether or not addictive drugs usurp the neuronal networks recruited by natural rewards by evaluating cocaine- and sucrose-associated ensembles within the same mouse. We used FosCreERT2/+/Ai14 transgenic mice to tag cells activated by and potentially encoding cocaine and sucrose seeking. We tagged ~1% of neurons in the core subregion of the accumbens (NAcore) activated during cue-induced seeking for cocaine or sucrose. The majority of tagged cells in the seeking ensembles were D1-MSNs, and specifically activated during seeking, not during extinction or when mice remained in the home cage. To compare different reward-specific ensembles within the same mouse, we used a dual cocaine and sucrose self-administration protocol allowing reward-specific seeking. Using this model, we found ~70% distinction between the cells constituting the cocaine- compared to the sucrose-seeking ensemble. Establishing that cocaine recruits an ensemble of NAcore neurons largely distinct from neurons recruited into an ensemble coding for sucrose seeking suggest a finely tuned specificity of ensembles. The findings allow further exploration of the mechanisms that transform reward-based positive reinforcement into maladaptive drug seeking.