Main effect of session, **P < 0.01
No main effect of group, P > 0.05
No significant interaction, P > 0.05
Šidák multiple comparisons test showed significant differences between groups for session 4, **P < 0.01, and 5, *P < 0.05.
Comparable Weight Loss Patterns Across Sexes with Sex-Based Weight Differences.
Increased Running Activity in ABA Mice, Influenced by Sex and Group Over Time.
Note: Due to imbalances in session duration and sex distribution across cohorts, no statistical analyses were conducted to assess sex differences. However, qualitative observations are provided.
Main effect of session, **P < 0.01
Main effect of group, *P < 0.05
Group by session interaction,****P < 0.0001
Šidák multiple comparisons test showed no significant group differences over the 6 sessions.
Main effect of session, **P < 0.01
No main effect of group, P > 0.05
Group by session interaction, ***P < 0.001
Šidák multiple comparisons test showed no significant group differences over sessions 3-6.
Main effect of group, *P < 0.05
No main effect of session, P > 0.05
Group by session interaction, **P < 0.01
Šidák multiple comparisons test showed no significant group differences over sessions 3-6.
Main effect of session, *P < 0.05
No main effect of group, P > 0.05
Group by session interaction, **P < 0.01.
Šidák multiple comparisons test showed no significant group differences over sessions 3-6.
Note: Due to the low sample size in the EXE group (n=1), statistical analyses were not conducted for male mice running activity. However, observations are described.
Mice that were restricted to 2 hours of food access per day exhibited significantly increased wheel running activity, particularly in the hours preceding food presentation.
The combination of food restriction and running wheel access led to greater weight loss in the ABA mice compared to the non-restricted EXE mice.
FAA likely plays a crucial role in ABA development for adolescent mice, as indicated by the increased activity levels during their sleep/light cycle and decreased activity levels upon food presentation.
The male mice took longer to acclimate to the running wheel and remained in the ABA paradigm longer, suggesting sex differences in ABA progression.
These findings show that the ABA paradigm in mice successfully induced some behaviors seen in human AN, supporting its use in studying the underlying neurobiology of AN.
We successfully established the activity-based anorexia paradigm in adolescent male and female C57BL/6J mice.
Future studies will investigate the neurobiological mechanisms underlying compulsive hyperactivity in ABA mice to identify potential psychopharmacological interventions to aid in the treatment of AN.