Giles Erin D, Hagman Jennifer, Pan Zhaoxing, MacLean Paul S, Higgins Janine A
Center for Human Nutrition, University of Colorado Anschutz Medical Campus, Aurora, CO USA ; Division of Endocrinology, Diabetes and Metabolism, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO USA.
Department of Psychiatry, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO USA.
Nutr Metab (Lond). 2016 Mar 1;13:18. doi: 10.1186/s12986-016-0077-y. eCollection 2016.
There is currently no standard clinical refeeding diet for the treatment of anorexia nervosa (AN). To provide the most efficacious AN clinical care, it is necessary to define the metabolic effects of current refeeding diets.
An activity-based model of anorexia nervosa (AN) was used in female rats. AN was induced over 7d by timed access to low fat (LF) diet with free access to a running wheel. Plasma hormones/metabolites and body composition were assessed at baseline, AN diagnosis (day 0), and following 28d of refeeding on LF diet. Energy balance and expenditure were measured via continuous indirect calorimetry on days -3 to +3.
AN induction caused stress as indicated by higher levels of corticosterone versus controls (p < 0.0001). The rate of weight gain during refeeding was higher in AN rats than controls (p = 0.0188), despite lower overall energy intake (p < 0.0001). This was possible due to lower total energy expenditure (TEE) at the time of AN diagnosis which remained significantly lower during the entire refeeding period, driven by markedly lower resting energy expenditure (REE). AN rats exhibited lower lipid accumulation in visceral adipose tissues (VAT) but much higher liver accumulation (62 % higher in AN than control; p < 0.05) while maintaining the same total body weight as controls. It is possible that liver lipid accumulation was caused by overfeeding of carbohydrate suggesting that a lower carbohydrate, higher fat diet may be beneficial during AN treatment. To test whether such a diet would be accepted clinically, we conducted a study in adolescent female AN patients which showed equivalent palatability and acceptability for LF and moderate fat diets. In addition, this diet was feasible to provide clinically during inpatient treatment in this population.
Refeeding a LF diet to restore body weight in female AN rats caused depressed TEE and REE which facilitated rapid regain. However, this weight gain was metabolically unhealthy as it resulted in elevated lipid accumulation in the liver. It is necessary to investigate the use of other diets, such as lower carbohydrate, moderate fat diets, in pre-clinical models to develop the optimal clinical refeeding diets for AN.
目前尚无用于治疗神经性厌食症(AN)的标准临床再喂养饮食方案。为了提供最有效的AN临床护理,有必要明确当前再喂养饮食的代谢效应。
在雌性大鼠中使用基于活动的神经性厌食症模型。通过限时获取低脂(LF)饮食并可自由使用跑步轮,在7天内诱导出AN。在基线、AN诊断时(第0天)以及在LF饮食再喂养28天后,评估血浆激素/代谢物和身体组成。在第-3天至+3天通过连续间接量热法测量能量平衡和消耗。
与对照组相比,较高水平的皮质酮表明AN诱导引起了应激(p < 0.0001)。尽管总体能量摄入量较低(p < 0.0001),但AN大鼠再喂养期间的体重增加率高于对照组(p = 0.0188)。这是可能的,因为在AN诊断时总能量消耗(TEE)较低,并且在整个再喂养期间仍显著较低,这是由明显较低的静息能量消耗(REE)驱动的。AN大鼠在内脏脂肪组织(VAT)中的脂质积累较低,但肝脏积累要高得多(AN比对照组高62%;p < 0.05),同时保持与对照组相同的总体重。肝脏脂质积累可能是由于碳水化合物过量喂养所致,这表明在AN治疗期间,低碳水化合物、高脂肪饮食可能有益。为了测试这种饮食在临床上是否会被接受,我们在青春期女性AN患者中进行了一项研究,结果表明LF饮食和中度脂肪饮食具有同等的适口性和可接受性。此外,这种饮食在该人群的住院治疗期间在临床上提供是可行的。
给雌性AN大鼠再喂养LF饮食以恢复体重会导致TEE和REE降低,这有助于快速恢复体重。然而,这种体重增加在代谢上是不健康的,因为它导致肝脏脂质积累增加。有必要在临床前模型中研究使用其他饮食,如低碳水化合物、中度脂肪饮食,以开发针对AN的最佳临床再喂养饮食方案。