A new animal model of binge eating: Key synergistic role of past caloric restriction and stress

被引:133
作者
Hagan, MM [1 ]
Wauford, PK [1 ]
Chandler, PC [1 ]
Jarrett, LA [1 ]
Rybak, RJ [1 ]
Blackburn, K [1 ]
机构
[1] Univ Alabama Birmingham, Dept Psychol, Behav Neurosci Div, Birmingham, AL 35294 USA
关键词
eating disorders; bulimia; binge eating disorder; stress-induced eating; rats; hyperphagia; reward; foot shock; opioids; behavior; refeeding; food intake; female; dieting;
D O I
10.1016/S0031-9384(02)00809-0
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Dieting and stress are important in the etiology and maintenance of eating disorders, and dieting strongly predicts stress-induced overeating in humans. We hypothesized that caloric restriction and stress interact in a unique manner to promote binge eating. To test this hypothesis, a group of young female rats were cycled through a restriction period (4 days of 66% of control food intake) followed by 6 days of free feeding prior to being stressed by acute foot shock. After three of these cycles, the food intake of rats exposed only to restriction (R), or only to stress (S), did not differ from controls. However, R+S rats that were restricted and refed, despite normal body weight and food intake after free feeding, engaged in a powerful bout of hyperphagia when stressed (Experiment 1). The R+S effect was replicated in an older group of rats (Experiment 2). The hyperphagia was characteristically binge-like, it constituted a 40% selective increase in highly palatable (HP) food (P<.001) over a discrete period of time (within 24 h post-stress), and reflected feeding for reward (higher HP:chow ratio) over metabolic need as occurred after restriction (higher chow:HP ratio). Subsequent experiments revealed that binge eating did not occur if only chow was available (Experiment 3) or if restriction-refeeding (R-R) did not proximally precede stress (Experiment 4). Experiment 5 revealed that a history of R-R cycles followed by only one stress episode was sufficient to increase intake to 53% above controls as early as 2 h after stress (P<.001). This animal model of binge eating should facilitate investigations into the neurochemical changes induced by dieting and environmental stress to produce disordered eating and provide a preclinical tool to test preventive strategies and treatments more relevant to bulimia nervosa, multiple cases of binge eating disorder (BED) and binge-purge type anorexia nervosa. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:45 / 54
页数:10
相关论文
共 77 条
[1]   HOW PATIENTS DESCRIBE BULIMIA OR BINGE EATING [J].
ABRAHAM, SF ;
BEUMONT, PJV .
PSYCHOLOGICAL MEDICINE, 1982, 12 (03) :625-635
[2]  
Akana S F, 1999, Stress, V3, P131, DOI 10.3109/10253899909001118
[3]   Effects of chronic stress on food acquisition, plasma hormones, and the estrous cycle of female rats [J].
Anderson, SM ;
Saviolakis, GA ;
Bauman, RA ;
Chu, KY ;
Ghosh, S ;
Kant, GJ .
PHYSIOLOGY & BEHAVIOR, 1996, 60 (01) :325-329
[4]   EFFECT OF DEPRESSED MOOD ON EATING AMONG OBESE AND NON-OBESE DIETING AND NON-DIETING PERSONS [J].
BAUCOM, DH ;
AIKEN, PA .
JOURNAL OF PERSONALITY AND SOCIAL PSYCHOLOGY, 1981, 41 (03) :577-585
[5]  
BERTIERE MC, 1984, PHARMACOL BIOCHEM BE, V20, P675, DOI 10.1016/0091-3057(84)90183-7
[6]   Feeding, drug abuse, and the sensitization of reward by metabolic need [J].
Carr, KD .
NEUROCHEMICAL RESEARCH, 1996, 21 (11) :1455-1467
[8]   Ketoconazole suppresses food restriction-induced increases in heroin self-administration in rats: Sex differences [J].
Carroll, ME ;
Campbell, UC ;
Heideman, P .
EXPERIMENTAL AND CLINICAL PSYCHOPHARMACOLOGY, 2001, 9 (03) :307-316
[9]   Limited access to a dietary fat option affects ingestive behavior but not body composition in male rats [J].
Corwin, RL ;
Wojnicki, FHE ;
Fisher, JO ;
Dimitriou, SG ;
Rice, HB ;
Young, MA .
PHYSIOLOGY & BEHAVIOR, 1998, 65 (03) :545-553
[10]   Binge eating and other psychopathology in patients with Type II diabetes mellitus [J].
Crow, S ;
Kendall, D ;
Praus, B ;
Thuras, P .
INTERNATIONAL JOURNAL OF EATING DISORDERS, 2001, 30 (02) :222-226