OBJECTIVE: Activity-based anorexia is a translational rodent model that results in severe weight loss, hyperactivity, and voluntary self-starvation. The goal of our investigation was to identify vulnerable and resistant phenotypes of activity-based anorexia in adolescent female rats. METHOD: Sprague-Dawley rats were maintained under conditions of restricted access to food (N = 64; or unlimited access, N = 16) until experimental exit, predefined as a target weight loss of 30-35% or meeting predefined criteria for animal health. Nonlinear mixed effects statistical modeling was used to describe wheel running behavior, time to event analysis was used to assess experimental exit, and a regressive partitioning algorithm was used to classify phenotypes. RESULTS: Objective criteria were identified for distinguishing novel phenotypes of activity-based anorexia, including a vulnerable phenotype that conferred maximal hyperactivity, minimal food intake, and the shortest time to experimental exit, and a resistant phenotype that conferred minimal activity and the longest time to experimental exit. DISCUSSION: The identification of objective criteria for defining vulnerable and resistant phenotypes of activity-based anorexia in adolescent female rats provides an important framework for studying the neural mechanisms that promote vulnerability to or protection against the development of self-starvation and hyperactivity during adolescence. Ultimately, future studies using these novel phenotypes may provide important translational insights into the mechanisms that promote these maladaptive behaviors characteristic of anorexia nervosa.
OBJECTIVE: Activity-based anorexia is a translational rodent model that results in severe weight loss, hyperactivity, and voluntary self-starvation. The goal of our investigation was to identify vulnerable and resistant phenotypes of activity-based anorexia in adolescent female rats. METHOD:Sprague-Dawley rats were maintained under conditions of restricted access to food (N = 64; or unlimited access, N = 16) until experimental exit, predefined as a target weight loss of 30-35% or meeting predefined criteria for animal health. Nonlinear mixed effects statistical modeling was used to describe wheel running behavior, time to event analysis was used to assess experimental exit, and a regressive partitioning algorithm was used to classify phenotypes. RESULTS: Objective criteria were identified for distinguishing novel phenotypes of activity-based anorexia, including a vulnerable phenotype that conferred maximal hyperactivity, minimal food intake, and the shortest time to experimental exit, and a resistant phenotype that conferred minimal activity and the longest time to experimental exit. DISCUSSION: The identification of objective criteria for defining vulnerable and resistant phenotypes of activity-based anorexia in adolescent female rats provides an important framework for studying the neural mechanisms that promote vulnerability to or protection against the development of self-starvation and hyperactivity during adolescence. Ultimately, future studies using these novel phenotypes may provide important translational insights into the mechanisms that promote these maladaptive behaviors characteristic of anorexia nervosa.
Authors: Eneda Pjetri; Ria de Haas; Simone de Jong; Cigdem Gelegen; Hugo Oppelaar; Linda A W Verhagen; Marinus J C Eijkemans; Roger A Adan; Berend Olivier; Martien J Kas Journal: PLoS One Date: 2012-11-30 Impact factor: 3.240
Authors: C Aoki; G Wable; T G Chowdhury; N A Sabaliauskas; K Laurino; N C Barbarich-Marsteller Journal: Neuroscience Date: 2014-01-18 Impact factor: 3.590
Authors: T Lee Gilman; W Anthony Owens; Christina M George; Lauren Metzel; Melissa Vitela; Livia Ferreira; Melodi A Bowman; Georgianna G Gould; Glenn M Toney; Lynette C Daws Journal: J Pharmacol Exp Ther Date: 2019-09-03 Impact factor: 4.030
Authors: Jeff A Beeler; Devry Mourra; Roseanna M Zanca; Abigail Kalmbach; Celia Gellman; Benjamin Y Klein; Rebecca Ravenelle; Peter Serrano; Holly Moore; Stephen Rayport; Susana Mingote; Nesha S Burghardt Journal: Biol Psychiatry Date: 2020-07-16 Impact factor: 13.382