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Updated: Jan 7, 2026

Using the Activity-based Anorexia Rodent Model to Study the Neurobiological Basis of Anorexia Nervosa
Published on: October 22, 2015
Reduced Ventral Tegmental Area GABA neuron output contributes to hyperactivity in the activity-based anorexia model
Fabien Ducrocq1,2, Lianne Delwel3, Nick Papavoine3
1Department of Translational Neuroscience, Brain Center, UMC Utrecht, Utrecht University, Utrecht, The Netherlands. fabien.ducrocq@inrae.fr.
Abstract:
Anorexia nervosa (AN) has the highest mortality among psychiatric disorders, with hyperactivity being one of the most persistent and deleterious symptoms. Increased dopamine transmission is linked to AN and hyperactivity, though the underlying mechanisms remain unclear. Local GABAergic neurons powerfully regulate the dopamine system but their involvement in AN is unknown. Using the activity-based anorexia (ABA) mouse model, we found that GABAergic transmission onto ventral tegmental area dopamine (VTADA) neurons modulates hyperactivity in female mice. Indeed, female mice exposed to the ABA model displayed higher firing rates in VTADA compared to controls, along with reduced GABAergic transmission onto VTADA cells and decreased excitability of VTAGABA neurons. Chemogenetic stimulation of GABA neurons excitability in the midbrain reduced hyperactivity and body weight loss in ABA mice, while reducing GABA neuron activity worsened this phenotype. In summary, decreased GABAergic control over VTA dopamine neurons contributes to development of hyperactivity in the ABA model.

