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Cluster of dopamine neurons drives eating behaviours

Florida State University researchers has revealed new insights into the role our brains play in why we vigorously seek food when we are hungry. Led by Assistant Professor of Psychology and Neuroscience Dr Xiaobing Zhang, the research team found specific neural circuits in the brain that control both hunger-driven, or homeostatic, and non-hunger-motivated, or hedonic, food-seeking behaviours. The study's findings suggest behavioural therapies may be an effective long-term solution for obesity and disordered eating, particularly binge-eating disorder.

ZI DA axonal terminals in the PVT were activated for food approach but inhibited during food consumption.(A) AAV-hSynapsin1-FLEx-axon-GCaMP6s was injected into ZI of TH-Cre mice for fiber-photometry imaging of ZI DA axon terminals in PVT. (B) Representative images show GCaMP6s was expressed in both ZI DA somas (top) and axonal terminals in the PVT (bottom). (C) Heatmap of normalized z-scores of ZI-PVT DA axonal terminals from 132 feeding trials of six ZITH-GCaMP mice. (D) z-scores of ZI-PVT DA axonal terminals aligned to the time of pellet retrieval from 132 trials of six ZITH-GCaMP mice. (E) Bar graph with data plots showing the averages of z-score at the time of −5, 0, and 5 s (n = 6 mice). One-way RM ANOVA with post hoc Bonferroni test. Credit: Science Advances (2023). DOI: 10.1126/sciadv.adi5326

"Behavioural therapy is some of the best treatment to combat eating disorders and obesity because it targets the behaviour’s roots and does not cause drug-induced side effects," said Zhang, whose research programme focuses on defining the connectivity and function of neural circuits that regulate food consumption and food-motivated behaviours.


Zhang's research team has found the zona incerta, a region deep in the brain's core that is not well understood, plays a critical role in controlling eating behaviours.


"Normally, food-seeking and eating behaviours are orchestrated by metabolic signals related to the body's energy state," Zhang said. "However, the brain's feeding centres, such as the zona incerta, may sometimes be activated by food-associated cues or conditioned environmental stimuli instead of relying only on energy needs to drive action."


Working in mouse models, Zhang, along with doctoral student, Qiying Ye, and research assistant Jeremiah Nunez, isolated a tiny group of dopamine neurons within the zona incerta that activate quickly to drive food-seeking behaviour when the body's energy levels dip and deactivate while food is consumed. Dopamine acts in the brain's reward system and current research suggests a group of specific dopamine neurons drives homeostatic food seeking.

The Zhang team intentionally silenced these dopamine neurons, which caused the study subjects to not seek food, even when hungry. However, subjects with silenced dopamine neurons still consumed a substantial amount of food when it was freely available.


The findings help researchers understand biologically complex phenomena at the root of eating-related topics such as obesity and eating disorders. The Zhang Lab's advances shed light on the neural mechanisms that lead to these conditions to enable psychologists and physicians to take different approaches and deliver more effective therapies and treatments to patients.


While conducting this study, Zhang also discovered that zona incerta dopamine neurons help develop contextual memories related to food seeking. Going forward, Zhang hopes to study what specific effects contextual memory has on eating regulation and behaviour.


"This is the first time the lab's research has been published in a journal we consider high-impact, and I feel inspired by the work we have done in my lab," Zhang said. "This publication is important for guiding the future direction of my research and my ability to add talented young scientists to the team."


The findings were published in the paper, Zona incerta dopamine neurons encode motivational vigor in food seeking', Science Advances. To access this paper, please click here

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